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The prediction of protein–ligand interactions and their corresponding binding free energy is a challenging task in structure-based drug design and related applications. Docking and scoring is broadly used to propose the binding mode and underlying interactions as well as to provide a measure for ligand affinity or differentiate between active and inactive ligands. Various studies have revealed that most docking software packages reliably predict the binding mode, although scoring remains a challenge. Here, a diverse benchmark data set of 99 matched molecular pairs (3D-MMPs) with experimentally determined X-ray structures and corresponding binding affinities is introduced. This data set was used to study the predictive power of 13 commonly used scoring functions to demonstrate the applicability of the 3D-MMP data set as a valuable tool for benchmarking scoring functions.
Background: Immigration has a strong impact on the development of health systems, medicine and science worldwide. Therefore, this article provides a descriptive study on the overall research output.
Methods: Utilizing the scientific database Web of Science, data research was performed. The gathered bibliometric data was analyzed using the established platform NewQIS, a benchmarking system to visualize research quantity and quality indices.
Findings: Between 1900 and 2016 a total of 6763 articles on immigration were retrieved and analyzed. 86 different countries participated in the publications. Quantitatively the United States followed by Canada and Spain were prominent regarding the article numbers. On comparing by additionally taking the population size into account, Israel followed by Sweden and Norway showed the highest performance. The main releasing journals are the Public Health Reports, the Journal of Immigrant and Minority Health and Social Science & Medicine. Over the decades, an increasing number of Public, Environmental & Occupational Health articles can be recognized which finally forms the mainly used subject area.
Conclusion: Considerably increasing scientific work on immigration cannot only be explained by the general increase of scientific work but is also owed to the latest development with increased mobility, worldwide crises and the need of flight and migration. Especially countries with a good economic situation are highly affected by immigrants and prominent in their publication output on immigration, since the countries’ publication effort is connected with the appointed expenditures for research and development. Remarkable numbers of immigrants throughout Europe compel medical professionals to consider neglected diseases, requires the public health system to restructure itself and finally promotes science.
The HCV NS5A protein plays multiple roles during viral replication, including viral genome replication and virus particle assembly. The crystal structures of the NS5A N-terminal domain indicated the potential existence of the NS5A dimers formed via at least two or more distinct dimeric interfaces. However, it is unknown whether these different forms of NS5A dimers are involved in its numerous functions. To address this question, we mutated the residues lining the two different NS5A dimer interfaces and determined their effects on NS5A self-interaction, NS5A-cyclophilin A (CypA) interaction, HCV RNA replication and infectious virus production. We found that the mutations targeting either of two dimeric interfaces disrupted the NS5A self-interaction in cells. The NS5A dimer-interrupting mutations also inhibited both viral RNA replication and infectious virus production with some genotypic differences. We also determined that reduced NS5A self-interaction was associated with altered NS5A-CypA interaction, NS5A hyperphosphorylation and NS5A subcellular localization, providing the mechanistic bases for the role of NS5A self-interaction in multiple steps of HCV replication. The NS5A oligomers formed via different interfaces are likely its functional form, since the residues at two different dimeric interfaces played similar roles in different aspects of NS5A functions and, consequently, HCV replication. In conclusion, this study provides novel insight into the functional significance of NS5A self-interaction in different steps of the HCV replication, potentially, in the form of oligomers formed via multiple dimeric interfaces.
The NF-κB-like velvet domain protein VosA (viability of spores) binds to more than 1,500 promoter sequences in the filamentous fungus Aspergillus nidulans. VosA inhibits premature induction of the developmental activator gene brlA, which promotes asexual spore formation in response to environmental cues as light. VosA represses a novel genetic network controlled by the sclB gene. Bfunction is antagonistic to VosA, because it induces the expression of early activator genes of asexual differentiation as flbC and flbD as well as brlA. The SclB controlled network promotes asexual development and spore viability, but is independent of the fungal light control. SclB interactions with the RcoA transcriptional repressor subunit suggest additional inhibitory functions on transcription. SclB links asexual spore formation to the synthesis of secondary metabolites including emericellamides, austinol as well as dehydroaustinol and activates the oxidative stress response of the fungus. The fungal VosA-SclB regulatory system of transcription includes a VosA control of the sclB promoter, common and opposite VosA and SclB control functions of fungal development and several additional regulatory genes. The relationship between VosA and SclB illustrates the presence of a convoluted surveillance apparatus of transcriptional control, which is required for accurate fungal development and the linkage to the appropriate secondary metabolism.
This thesis investigates whether professionals on the global financial markets, such as investment bankers, traders, and analysts, form a global social class.
Over recent decades, rising inequality has reinvigorated interest in issues of class. Despite the experience of world-wide economic crises demonstrating the global reach of the contemporary economy, the research areas of globalisation and class remain surprisingly disengaged from each other. Especially the question of global class formation remains underexplored.
The first part of this thesis examines why the issue of globalisation remains a niche within research on class. Therefore, the theoretical foundations of the dominant approaches to class are investigated, identifying the causes for the implicit “methodological nationalism” of modern mainstream class analysis in the underlying theories of the economy and social action. Vice-versa, an examination of globalisation theory shows that similar obstacles persist in the theoretical reasoning on inequality from a global perspective, precluding a conceptualisation of global class formation. In dialogue with the few existing approaches to conceptualize class on a global level, a framework for the study of global class formation based on Pierre Bourdieu’s notion of social fields is developed.
In part two of the thesis this framework is employed to examine empirically, whether the global field of finance is currently the source for the formation of a global financial class. The field of finance as the most globalised economic sector is a paradigmatic case for studying the formation of a global class. An interview study on the career trajectories of financial professionals from Frankfurt and Sydney uncovers that despite the legacy of national economic specificities on the institutional level, financial actors draw in their social praxis on global forms of social, cultural, and economic capital and have developed a common culture, worldview, praxis, and habitus, delineating the formation of a global financial class.
Five new species belonging to Hermatomyces (Hermatomycetaceae, Pleosporales) are described based on morphological investigations of specimens collected on rotten twigs and stems of various plants in Panama as well as phylogenetic analyses of sequence data of nuclear ribosomal and protein coding genes (EF1-α, RPB2, β-TUB). The new species are described as: Hermatomyces bifurcatus, H. constrictus, H. megasporus, H. sphaericoides, and H. verrucosus spp. nov. Previously described species such as H. sphaericus and H. tucumanensis were identified among the studied specimens. The new combination, H. reticulatus, is made for Subicularium reticulatum based on examination of the holotype and fresh collections. Hermatomyces subiculosus, originally described from Thailand, is reduced to synonymy with H. reticulatus; H. tectonae is synonymized under H. sphaericus based on morphological and molecular evidence; and H. chiangmaiensis and H. thailandicus are considered later synonyms of H. krabiensis and H. indicus, respectively. The type material of Scyphostroma mirum was found to be conspecific with H. tucumanensis and, therefore, the generic name Hermatomyces should be conserved or protected against the older name Scyphostroma and the binomial H. tucumanensis against S. mirum. Sixteen species of Hermatomyces are recognized, their distinctive characteristics are highlighted in line drawings and a key is provided for their identification. The peculiar morphology and consistent phylogeny of new and previously known Hermatomyces species supports the recognition of the recently introduced monotypic family Hermatomycetaceae as a well delimited monophyletic taxon within the order Pleosporales.
Leaf-stripe smuts on grasses are a highly polyphyletic group within Ustilaginomycotina, occurring in three genera, Tilletia, Urocystis, and Ustilago. Currently more than 12 Ustilago species inciting stripe smuts are recognised. The majority belong to the Ustilago striiformis-complex, with about 30 different taxa described from 165 different plant species. This study aims to assess whether host distinct-lineages can be observed amongst the Ustilago leaf-stripe smuts using nine different loci on a representative set. Phylogenetic reconstructions supported the monophyly of the Ustilago striiformis-complex that causes leaf-stripe and the polyphyly of other leaf-stripe smuts within Ustilago. Furthermore, smut specimens from the same host genus generally clustered together in well-supported clades that often had available species names for these lineages. In addition to already-named lineages, three new lineages were observed, and described as new species on the basis of host specificity and molecular differences: namely Ustilago jagei sp. nov. on Agrostis stolonifera, U. kummeri sp. nov. on Bromus inermis, and U. neocopinata sp. nov. on Dactylis glomerata.
Background: Recent epidemics have entailed global discussions on revamping epidemic control and prevention approaches. A general consensus is that all sources of data should be embraced to improve epidemic preparedness. As a disease transmission is inherently governed by individual-level responses, pathogen dynamics within infected hosts posit high potentials to inform population-level phenomena. We propose a multiscale approach showing that individual dynamics were able to reproduce population-level observations.
Methods: Using experimental data, we formulated mathematical models of pathogen infection dynamics from which we simulated mechanistically its transmission parameters. The models were then embedded in our implementation of an age-specific contact network that allows to express individual differences relevant to the transmission processes. This approach is illustrated with an example of Ebola virus (EBOV).
Results: The results showed that a within-host infection model can reproduce EBOV’s transmission parameters obtained from population data. At the same time, population age-structure, contact distribution and patterns can be expressed using network generating algorithm. This framework opens a vast opportunity to investigate individual roles of factors involved in the epidemic processes. Estimating EBOV’s reproduction number revealed a heterogeneous pattern among age-groups, prompting cautions on estimates unadjusted for contact pattern. Assessments of mass vaccination strategies showed that vaccination conducted in a time window from five months before to one week after the start of an epidemic appeared to strongly reduce epidemic size. Noticeably, compared to a non-intervention scenario, a low critical vaccination coverage of 33% cannot ensure epidemic extinction but could reduce the number of cases by ten to hundred times as well as lessen the case-fatality rate.
Conclusions: Experimental data on the within-host infection have been able to capture upfront key transmission parameters of a pathogen; the applications of this approach will give us more time to prepare for potential epidemics. The population of interest in epidemic assessments could be modelled with an age-specific contact network without exhaustive amount of data. Further assessments and adaptations for different pathogens and scenarios to explore multilevel aspects in infectious diseases epidemics are underway.
In several tumor entities, transketolase-like protein 1 (TKTL1) has been suggested to promote the nonoxidative part of the pentose phosphate pathway (PPP) and thereby to contribute to a malignant phenotype. However, its role in glioma biology has only been sparsely documented. In the present in vitro study using LNT-229 glioma cells, we analyzed the impact of TKTL1 gene suppression on basic metabolic parameters and on survival following oxygen restriction and ionizing radiation. TKTL1 was induced by hypoxia and by hypoxia-inducible factor-1α (HIF-1α). Knockdown of TKTL1 via shRNA increased the cells’ demand for glucose, decreased flux through the PPP and promoted cell death under hypoxic conditions. Following irradiation, suppression of TKTL1 expression resulted in elevated levels of reactive oxygen species (ROS) and reduced clonogenic survival. In summary, our results indicate a role of TKTL1 in the adaptation of tumor cells to oxygen deprivation and in the acquisition of radioresistance. Further studies are necessary to examine whether strategies that antagonize TKTL1 function will be able to restore the sensitivity of glioma cells towards irradiation and antiangiogenic therapies in the more complex in vivo environment.
Cardiac sarcoidosis is a rare immunologic disease causing heart involvement in 5% of patients. Cardiac sarcoidosis may manifest clinically as a cardiomyopathy with impaired left ventricular (LV) function or as tachyarrhythmias or bradyarrhythmias. On autopsy, cardiac granulomas can be found in approximately 25% of patients. The most common location for granulomas and scars is the LV free wall, followed by the intraventricular septum, often with involvement of the conduction system. ...
Temperature- and field-dependent 1H-, 19F-, and 79,81Br-NMR measurements together with zero - field 79,81Br-NQR measurements on polycrystalline samples of barlowite, Cu4(OH)6FBr are conducted to study the magnetism and possible structural distortions on a microscopic level. The temperature dependence of the 79,81Br-NMR spin-lattice relaxation rates 1/T1 indicate a phase transition at TN ≃ 15 K which is of magnetic origin, but with an unusually weak slowing down of fluctuations below TN. Moreover, 1/T1T scales linear with the bulk susceptibility which indicates persisting spin fluctuations down to 2 K. Quadupolare resonance (NQR) studies reveal a pair of zero-field NQR- lines associated with the two isotopes of Br with the nuclear spins of I = 3/2. Quadrupole coupling constants of vQ ≃ 28.5 MHz and 24.7 MHz for 79Br- and 81Br-nuclei are determined from Br-NMR and the asymmetry parameter of the electric field gradient was estimated to η ≃ 0.2. The Br-NQR lines are consistent with our findings from Br-NMR and they are relatively broad, even above TN. This broadening and the relative large η value suggests a symmetry reduction at the Br- site reflecting the presence of a local distortion in the lattice. Our density-functional calculations show that the displacements of Cu2 atoms located between the kagome planes do not account for this relatively large η. On the other hand, full structural relaxation, including the deformation of kagome planes, leads to a better agreement with the experiment.
Exploring the ability of acoustic infant cry analysis for discriminating developmental pathologies
(2018)
This thesis aims at exploring the ability of acoustic infant cry analysis for discriminating developmental pathologies. Cries of healthy infants as well as cries of infants suffering from cleft lip and palate, hearing impairment, laryngomalacia, asphyxia and brain damage were recorded and acoustically analyzed. The acoustic properties of the infant cries were identified and tested on their suitability to predict the health state of the infants in an reliable, valid and objective way.
To test the reliability of infant cry analysis, Krippendorff’s Alpha coefficient was calculated to test how homogeneous cries of healthy infants as well as cries of infants suffering from various pathologies are.
To asses if valid methods exist for classifying infant cries, different approaches that can be used to differentiate between the groups and to predict the health state of the infants — e.g., analysis of variances, supervised-learning models and auditory discrimination by human listeners — were tested on their validity.
The objectivity of computer-based and human-based classification approaches was explored and techniques to enhance the objectivity for both approaches are proposed.
Computer-based approaches are more objective and reached higher sensitivity and specificity values in their classification to predict the health state of the infants. Especially C5.0 decision trees reached high and therefore promising classification results, even though infant cries have a great statistical spread and can be seen as very heterogeneous and are therefore not very reliable in general.
Tubulogenesis is essential for the formation and function of internal organs. One such organ is the trachea, which allows gas exchange between the external environment and the lungs. However, the cellular and molecular mechanisms underlying tracheal tube development remain poorly understood. Here, we show that the potassium channel KCNJ13 is a critical modulator of tracheal tubulogenesis. We identify Kcnj13 in an ethylnitrosourea forward genetic screen for regulators of mouse respiratory organ development. Kcnj13 mutants exhibit a shorter trachea as well as defective smooth muscle (SM) cell alignment and polarity. KCNJ13 is essential to maintain ion homeostasis in tracheal SM cells, which is required for actin polymerization. This process appears to be mediated, at least in part, through activation of the actin regulator AKT, as pharmacological increase of AKT phosphorylation ameliorates the Kcnj13-mutant trachea phenotypes. These results provide insight into the role of ion homeostasis in cytoskeletal organization during tubulogenesis.
Background: Most smokers start smoking during their early adolescence, often with the idea that smoking is glamorous. Interventions that harness the broad availability of mobile phones as well as adolescents' interest in their appearance may be a novel way to improve school-based prevention. A recent study conducted in Germany showed promising results. However, the transfer to other cultural contexts, effects on different genders, and implementability remains unknown.
Objective: In this observational study, we aimed to test the perception and implementability of facial-aging apps to prevent smoking in secondary schools in Brazil in accordance with the theory of planned behavior and with respect to different genders.
Methods: We used a free facial-aging mobile phone app ("Smokerface") in three Brazilian secondary schools via a novel method called mirroring. The students’ altered three-dimensional selfies on mobile phones or tablets and images were "mirrored" via a projector in front of their whole grade. Using an anonymous questionnaire, we then measured on a 5-point Likert scale the perceptions of the intervention among 306 Brazilian secondary school students of both genders in the seventh grade (average age 12.97 years). A second questionnaire captured perceptions of medical students who conducted the intervention and its conduction per protocol.
Results: The majority of students perceived the intervention as fun (304/306, 99.3%), claimed the intervention motivated them not to smoke (289/306, 94.4%), and stated that they learned new benefits of not smoking (300/306, 98.0%). Only a minority of students disagreed or fully disagreed that they learned new benefits of nonsmoking (4/306, 1.3%) or that they themselves were motivated not to smoke (5/306, 1.6%). All of the protocol was delivered by volunteer medical students.
Conclusions: Our data indicate the potential for facial-aging interventions to reduce smoking prevalence in Brazilian secondary schools in accordance with the theory of planned behavior. Volunteer medical students enjoyed the intervention and are capable of complete implementation per protocol.
The identification of inhibitors of eukaryotic protein biosynthesis, which are targeting single translation factors, is highly demanded. Here we report on a small molecule inhibitor, gephyronic acid, isolated from the myxobacterium Archangium gephyra that inhibits growth of transformed mammalian cell lines in the nM range. In direct comparison, primary human fibroblasts were shown to be less sensitive to toxic effects of gephyronic acid than cancer-derived cells. Gephyronic acid is targeting the protein translation system. Experiments with IRES dual luciferase reporter assays identified it as an inhibitor of the translation initiation. DARTs approaches, co-localization studies and pull-down assays indicate that the binding partner could be the eukaryotic initiation factor 2 subunit alpha (eIF2α). Gephyronic acid seems to have a different mode of action than the structurally related polyketides tedanolide, myriaporone, and pederin and is a valuable tool for investigating the eukaryotic translation system. Because cancer derived cells were found to be especially sensitive, gephyronic acid could potentially find use as a drug candidate.
Ludwig van Beethoven im Film
(2018)
Sissi im Film
(2018)
TEMPO spin labels protected with 2-nitrobenzyloxymethyl groups were attached to the amino residues of three different nucleosides: deoxycytidine, deoxyadenosine, and adenosine. The corresponding phosphoramidites could be incorporated by unmodified standard procedures into four different self-complementary DNA and two RNA oligonucleotides. After photochemical removal of the protective group, elimination of formic aldehyde and spontaneous air oxidation, the nitroxide radicals were regenerated in high yield. The resulting spin-labeled palindromic duplexes could be directly investigated by PELDOR spectroscopy without further purification steps. Spin–spin distances measured by PELDOR correspond well to the values obtained from molecular models.
Die Straßen deutscher Städte werden überwiegend vom Automobil dominiert, was nicht nur die gebaute Umwelt prägt, sondern auch die politischen Entscheidungen beeinflusst, wenn es um die Verteilung des Straßenraumes geht. Dass jedoch am Anfang der Mobilität das Zufußgehen steht und ein gut geplanter städtischer Fußverkehr nicht nur einen Beitrag zur Sicherheit der Fußgänger*innen leistet, sondern auch die Zukunft urbaner Mobilität gewährleistet, wird oft vergessen. Obwohl der Fußverkehr zahlreiche Potentiale bietet, bekommt er im öffentlichen Raum deutlich weniger Entfaltungsspielraum zur Verfügung gestellt. Die Zufußgehenden werden dort häufig kanalisiert und an den Rand gedrängt, was Einfluss auf ihr Verhalten nimmt. Diese Marginalisierung der Fußgänger*innen wird zusätzlich hervorgerufen durch eine geringe Beachtung jener in der städtischen Planung und Politik sowie in der Wissenschaft und Gesellschaft. Demnach stehen sie im Konfliktverhältnis zur persistenten und sozial konstruierten Struktur der Straße.
Die vorliegende Untersuchung überprüft, warum die Fortbewegung zu Fuß in der gebauten Straßenumwelt und ihrer Raumaufteilung im Vergleich zu anderen Verkehrsmitteln eine untergeordnete Rolle spielt und welchen Einfluss der planerische und politische Umgang und die Gestaltung des Straßenraumes darauf nimmt. Dies geschieht mittels eines Fallbeispiels in Frankfurt am Main, der Schweizer Straße. Im Rahmen der Studie werden Ergebnisse aus teilnehmenden Beobachtungen der Zufußgehenden der Schweizer Straße und deren Verhaltensweisen im öffentlichen Straßenraum sowie aus qualitativen Interviews mit Expert*innen der gebauten Straßenumwelt Frankfurts zusammengetragen. Das übergeordnete Ziel der Arbeit ist, ein Verständnis für die Wechselwirkung zwischen Raumstruktur, planerischem Einfluss und Mobilität zu entwickeln sowie die Konflikte der Raumaufteilung für die Fußgänger*innen herauszuarbeiten, um den Fußverkehr gezielter fördern zu können.
Dinge in Texten haben maßgeblich an der Konstruktion imaginärer Welten teil. Sie können intradiegetisch angefasst werden, sie riechen, haben ein spezifisches Gewicht und doch sind sie für die Leser in erster Linie: durch Zeichen repräsentierte Dinge. So einfach und so komplex lässt sich die doppelbödige Ausgangslage beschreiben, auf der die folgenden Überlegungen gründen. Denn auf diese Beobachtung kann Literaturwissenschaft in unterschiedlicher Weise reagieren: An einem Ende der Skala beschäftigt sie sich hauptsächlich mit der Zeichenhaftigkeit von repräsentierten Dingen, den Verweischarakteristiken, Funktionen und Bedeutungen, am anderen mit der Materialität, der Stofflichkeit und Widerständigkeit. Beide Pole haben ihre Verfechter, jeder der Ansätze seine Tradition und Konjunkturen. Bevor dieser Hintergrund, die Begrifflichkeit und der Forschungsstand erläutert werden, stehen in der Folge zwei literarische Beispiele im Zentrum, an denen gezeigt wird, welche Fragen sich mit literarischen Dingen stellen. Ludwig Tiecks 'Des Lebens Überfluß' (1838) und Ilija Trojanows 'Auf der Flucht' (2017) entstammen ganz unterschiedlichen Epochen und Kontexten, deshalb lässt sich an ihnen auch eine Bandbreite von Fragestellungen aufzeigen.
Das Peptidhormon Orexin (Hypokretin), das insbesondere in Neuronen des lateralen Hypothalamus synthetisiert wird, hat nach neueren Untersuchungen neben dem Einfluss auf das Essverhalten eine entscheidende Funktion im Schlaf-Wach Verhalten. In optogenetischen Untersuchungen, in denen modifizierte Zellen durch Licht aktiviert werden, konnte durch die Hochregulation von Orexin eine deutliche Wachheits- und Aktivitätszunahme der Tiere verzeichnet werden. Bei erhöhter MCH Freisetzung war eine vermehrte Schlafneigung beobachtet worden. Orexin und MCH scheinen demnach gegensinnige Funktionen in der Schlaf-Wach Regulation einzunehmen.
Mit der vorliegenden Arbeit wurden genauere Einblicke in das orexinerge System im Gehirn von zwei unterschiedlichen Mäusestämmen gewonnen. Es ist nach unserem Wissensstand die erste Arbeit, die das Reaktivitätsmuster von Orexin und MCH bei C3H- und C57BL-Mäusen im Hinblick auf Schlaf und Schlafentzug beleuchtet. Der Vergleich zwischen den Mäusestämmen ist im Besonderen interessant, weil die C57BL-Mäuse das pineale Schlafhormon Melatonin nicht bilden.
Beide Mäusestämme wurden nach Adaptation während drei unterschiedlicher Funktionszustände semiquantitativ immunhistochemisch untersucht: im Schlaf, im aktiven Zustand sowie nach 6-stündigem Schlafentzug. Nach Fixierung der Gehirne wurden die angefertigten Hirnschnitte immunhistochemisch gefärbt und mikroskopiert. Die Semi-Quantifizierung der Immunreaktivität erfolgte durch eine etablierte Bildbearbeitungsmethodik.
Das Verteilungsmuster Orexin- und MCH-ir Neurone ist zwischen den jeweiligen Mäusestämmen gleich und zeigt eine gegenseitige Innervation. Dies spricht für eine geregelte Interaktion beider Botenstoffsysteme.
Weiterhin zeigte sich eine deutliche Schlaf-physiologische Korrelation orexinerger Neurone mit der höchsten Immunreaktivität während der Wachheit. Es konnte jedoch kein Unterschied der Immunreaktivität in Bezug auf Lokalisation und Stadien zwischen C3H- und C57BL-Mäusen nachgewiesen werden, sodass davon auszugehen ist, dass die Melatonindefizienz der C57BL keine bedeutende Rolle in der zirkadianen Regulation von Orexin spielt.
Im Gegensatz zu Orexin konnte kein signifikanter Unterschied in der Immunreaktivität MCH-ir Neurone zu den unterschiedlichen Vigilanzstadien festgestellt werden.
Vermutlich spielt die relative Inaktivität von Orexin in Kombination mit aktiver Sekretion von MCH eine wichtige Rolle in der Induktion und Kontrolle von Schlaf.
Es sind noch viele Fragen offen; insbesondere die Interaktion zwischen Wachheit- und Schlaf-induzierenden Neuronen deren Regulation. Auch der Einfluss vom Nucleus suprachiasmaticus auf Oreginerge/MCHerge Neurone, sowie das Verhältnis von Melatonin zu Orexin und MCH bedarf weiterer Forschungen.
The thesis deals with the analysis and modeling of point processes emerging from different experiments in neuroscience. In particular, the description and detection of different types of variability changes in point processes is of interest.
A non-stationary rate or variance of life times is a well-known problem in the description of point processes like neuronal spike trains and can affect the results of further analyses requiring stationarity. Moreover, non-stationary parameters might also contain important information themselves. The goal of the first part of the thesis is the (further) development of a technique to detect both rate and variance changes that may occur in multiple time scales separately or simultaneously. A two-step procedure building on the multiple filter test (Messer et al., 2014) is used that first tests the null hypothesis of rate homogeneity allowing for an inhomogeneous variance and that estimates change points in the rate if the null hypothesis is rejected. In the second step, the null hypothesis of variance homogeneity is tested and variance change points are estimated. Rate change points are used as input. The main idea is the comparison of estimated variances in adjacent windows of different sizes sliding over the process. To determine the rejection threshold functionals of the Brownian motion are identified as limit processes under the null of variance homogeneity. The non-parametric procedure is not restricted to the case of at most one change point. It is shown in simulation studies that the corresponding test keeps the asymptotic significance level for a wide range of parameters and that the test power is remarkable. The practical applicability of the procedure is underlined by the analysis of neuronal spike trains.
Point processes resulting from experiments on bistable perception are analyzed in the second part of the thesis. Visual illusions allowing for than more possible perception lead to unpredictable changes of perception. In the thesis data from (Schmack et al., 2015) are used. A rotating sphere with switching perceived rotation direction was presented to the participants of the study. The stimulus was presented continuously and intermittently, i.e., with short periods of „blank display“ between the presentation periods. There are remarkable differences in the response patterns between the two types of presentation. During continuous presentation the distribution of dominance times, i.e., the intervals of constant perception, is a right-skewed and unimodal distribution with a mean of about five seconds. In contrast, during intermittent presentation one observes very long, stable dominance times of more than one minute interchanging with very short, unstable dominance times of less than five seconds, i.e., an increase of variability.
The main goal of the second part is to develop a model for the response patterns to bistable perception that builds a bridge between empirical data analysis and mechanistic modeling. Thus, the model should be able to describe both the response patterns to continuous presentation and to intermittent presentation. Moreover, the model should be fittable to typically short experimental data, and the model should allow for neuronal correlates. Current approaches often use detailed assumptions and large parameter sets, which complicate parameter estimation.
First, a Hidden Markov Model is applied. Second, to allow for neuronal correlates, a Hierarchical Brownian Model (HBM) is introduced, where perception is modeled by the competition of two neuronal populations. The activity difference between these two populations is described by a Brownian motion with drift fluctuating between two borders, where each first hitting time causes a perceptual change. To model the response patterns to intermittent presentation a second layer with competing neuronal populations (coding a stable and an unstable state) is assumed. Again, the data are described very well, and the hypothesis that the relative time in the stable state is identical in a group of patients with schizophrenia and a control group is rejected. To sum up, the HBM intends to link empirical data analysis and mechanistic modeling and provides interesting new hypotheses on potential neuronal mechanisms of cognitive phenomena.
Hippodamia variegata (Goeze) (Coleoptera: Coccinellidae), a Palearctic lady beetle that has become established in North America, is reported for the first time from the state of Iowa, U.S.A. The earliest specimen of H. variegata from Iowa was collected in 2009, with two subsequent specimens in 2012. Collection records of an advancing, non-native species like H. variegata are important for determining comparative rates of geographic spread across various regions and understanding its invasion dynamics.
Modellierung der klimatischen Habitateignung verschiedener krankheitsübertragender Vektorarten
(2018)
Der Klimawandel hat einen starken Einfluss auf die Verbreitungsgebiete von Arten. Infolgedessen kann sich das Verbreitungsgebiet von Arten verschieben, einschränken oder ausweiten. Bei thermophilen Arten wird vermutet, dass sie von den klimatischen Änderungen profitieren und sie sich wahrscheinlich ausbreiten werden. Eine solche Ausbreitung, wozu auch die Einwanderung von gebietsfremden Arten zählt, hätte nicht nur zahlreiche Konsequenzen für diese Ökosysteme, sondern könnte sich auch zu einem ernsten Gesundheitsrisiko entwickeln, wenn es sich bei den einwandernden Neobiota um Vektorarten handelt.
Stechmücken und Sandmücken, als blutsaugende Insekten, zählen zu den bekanntesten Vektorarten. Sie sind in der Lage, eine Vielzahl von Infektionskrankheiten wie das Denguefieber oder das Gelbfieber, aber auch protozoische Parasiten wie "Leishmania"-Arten zu übertragen. Als thermophile Arten sind viele dieser Vektoren aktuell in ihrer Verbreitung weitgehend auf tropische und subtropische Gebiete beschränkt. Eine Einwanderung in gemäßigtere Gebiete kann zu einer Einschleppung der durch sie übertragenden Erreger führen und damit zum Ausbruch von Infektionskrankheiten. Aufgrund der medizinischen Relevanz dieser Arten ist es essentiell, die räumliche Verbreitung, sowie die abiotischen Ansprüche der Vektorarten zu kennen, um deren mögliche Ausbreitung nachzuvollziehen.
Vor diesem Hintergrund beschäftigte sich die vorliegende kumulative Dissertation mit den klimawandelinduzierten Änderungen der Habitateignung verschiedener medizinisch relevanter Vektorarten. Dabei wurden die zwei invasiven Stechmückenarten "Aedes albopictus" (I-III) und "Aedes japonicus" (III), sowie zehn in Europa bereits vorkommende Sandmückenarten der Gattung "Phlebotomus" (IV), untersucht. Die Arbeit basiert auf vier (ISI-) Publikationen. Unter Verwendung ökologischer Nischenmodellierung wurden geeignete Gebiete unter aktuellen und zukünftigen Klimabedingungen bestimmt. Um dabei sowohl räumliche als auch zeitliche Aspekte zu berücksichtigen, wurden mehrere räumliche Skalen (Deutschland und Europa), sowie Zeitperioden (2030, 2050 und 2070) betrachtet. Des Weiteren wurden verschiedene Ansätze (einzelne Algorithmen und Ensemble-Modelle) zur Modellierung der Habitateignung verwendet.
Die Ergebnisse dieser Dissertation zeigen eine zukünftige klimawandelbedingte Ausweitung der geeigneten Gebiete für viele der betrachteten Vektorarten. So konnte gezeigt werden, dass die Habitateignung für "Aedes albopictus" in Deutschland (I) und in Europa (III) zukünftig deutlich zunimmt. Auch für die Sandmückenarten "Phlebotomus alexandri", "Phlebotomus neglectus", "Phlebotomus papatasi", "Phlebotomus perfiliewi" und "Phlebotomus tobbi" konnte eine deutliche Zunahme der klimatisch geeigneten Gebieten projiziert werden (IV).
Lediglich Arten, wie die Asiatische Buschmücke "Aedes japonicus" (III) und auch kältetolerantere Sandmücken, wie "Phlebotomus ariasi" und "Phlebotomus mascittii" (IV) scheinen weniger von diesen klimatischen Veränderungen zu profitieren und könnten in Zukunft sogar aktuell geeignete Gebiete verlieren (klimawandelinduzierte Arealverkleinerung). Bei "Aedes japonicus" konnte dies auf eine engeren Nische mit einem Optimum bei vergleichsweise niedrigen Temperaturen zurückgeführt werden (III).
Am Beispiel von "Aedes albopictus" wurden ferner Umweltfaktoren identifiziert, die die Verbreitung der Art limitieren (II). Als wärmeliebende Art spielen bei "Aedes albopictus" in Mitteleuropa insbesondere die niedrigen Temperaturen eine Rolle, während in Zukunft die Sommertrockenheit in Südeuropa zunehmend eine Rolle spielen könnte.
Nischenmodellierung stellt trotz ihrer vereinfachenden Annahmen und Unsicherheiten, eine hilfreiche Methode zur Untersuchung klimawandelinduzierter Arealverschiebungen dar. Mit Hilfe der Modellierungsergebnisse konnten Gebiete mit einem hohen Etablierungsrisiko für die Vektorarten identifiziert werden, welche daher im Fokus künftiger Überwachungsprogramme stehen sollten. In Zukunft könnten mehr Vektorarten geeignete Bedingungen in Mitteleuropa finden, wodurch die Vektordiversität zunehmen wird. Dadurch könnte auch das Risiko für einen Ausbruch der durch die Vektoren übertragenen Krankheiten steigen.
Auch wenn das Vorhandensein eines kompetenten Vektors eine unerlässliche Voraussetzung für den Ausbruch einer Infektionskrankheit darstellt, gibt es noch weitere Faktoren, wie das Vorhandensein des Erregers. In Bezug auf die Risikoabschätzung vektorassoziierter Krankheiten sollten neben der Verbreitung des Vektors und des Erregers auch die abiotischen Bedingungen für die Entwicklung des Erregers berücksichtigt werden. Neben neu eingewanderten Arten sollten zudem auch die heimischen Arten in Bezug auf ihre Vektorkompetenz untersucht werden, da diese ebenfalls als potentielle Vektoren dienen und somit das Gesundheitsrisiko weiter erhöhen könnten.
Based on morphological features of the adult female, the Brazilian soft scale, Mesolecanium ferum Hempel, 1920 (= Toumeyella ferum) (Hemiptera: Coccomorpha: Coccidae) is transferred to the genus Neotoumeyella Kondo and Williams, 2009, as Neotoumeyella ferum (Hempel), comb. nov. The genus Neotoumeyella is rediagnosed in order to accommodate the unique features of M. ferum and an updated key to the six species of the genus is provided. An English translation of the Spanish redescription of M. ferum (as T. ferum) by Granara de Willink (2012) is also provided, with the author’s comments and interpretations.
A combination of five characters supports the arrangement of three species in the Anthocharis sara complex (Lepidoptera: Pieridae: Pierinae: Anthocharidini) consisting of Anthocharis sara Lucas, 1852 (Sara orangetip), Anthocharis thoosa Scudder, 1878 (southwestern orangetip), and Anthocharis julia W.H. Edwards, 1872 (Julia orangetip). These five characters include adult phenotypes, fifth instar larval coloration, pupal cone curvature and color, number of overwintering cycles, and interspecific contact zone behavior. This taxonomic treatment is generated from extensive life history studies from 12 western U.S. states through most of the sara complex distribution.
Diese Arbeit beschäftigt sich mit inversen Problemen für partielle Differentialgleichungen. Moderne Lösungsverfahren solcher inversen Probleme müssen die zugehörige partielle Differentialgleichung (PDGL) oft sehr häufig lösen. Mit Hinblick auf die Rechenzeit solcher Verfahren stellt das häufige Lösen der PDGL den Hauptanteil der benötigten Rechenzeit dar. Daraus resultiert die Grundidee dieser Arbeit: es sollen Lösungsverfahren von inversen Problemen beschleunigt werden, indem die für die Vorwärtslösung benötigte Rechenzeit verringert wird. Genauer gesagt soll anstatt der Vorwärtslösung eine Approximation an diese, welche kostengünstig zu berechnen ist, verwendet werden. Für die Bestimmung einer kostengünstigen Annäherung an die Vorwärtslösung wird die Reduzierte Basis Methode, eine Modellreduktionstechnik, verwendet.
Das Ziel der klassischen Reduzierten Basis Methode ist es einen globalen Reduzierte Basis Raum (RB-Raum) zu konstruieren. Dabei handelt es sich um einen niedrigdimensionalen Teilraum des Lösungsraumes der PDGL, welcher für jeden Parameter aus dem Parameterraum eine gute Näherung der PDGL-Lösung liefert. Eine beispielhafte Methode zur Konstruktion eines solchen Raumes ist es, geschickt Parameter auszuwählen und die dazu gehörigen PDGL-Lösungen als Basisvektoren des RB-Raumes zu verwenden. Die orthogonale Projektion der PDGL auf diesen RB-Raum liefert die entsprechenden Reduzierte Basis Lösungen. Das Besondere in dieser Arbeit ist, dass die betrachteten PDGLn einen sehr hochdimensionalen und unbeschränkten Parameterraum besitzen, und es ist bekannt, dass dies für die Reduzierte Basis Methode eine immense Schwierigkeit darstellt.
In Kapitel 1 wird ein schlechtgestelltes inverses Modellproblem, die Rekonstruktion der Wärmeleitfähigkeit eines Gegenstandes aus der Messung der Temperatur desselben, eingeführt und das nichtlineare Landweber-Verfahren als iteratives Regularisierungsverfahren zur Lösung dieses inversen Problems vorgestellt. Die Grundlagen der Reduzierten Basis Methode werden dargelegt und es wird erläutert, warum die klassische Variante der Methode in diesem Kontext der Bildrekonstruktion versagt. Daraufhin wird der neuartig Ansatz, ein adaptiver Reduzierte Basis Ansatz, entwickelt. Die folgenden Schritte bilden die Grundlage dieses adaptiven Reduzierte Basis Ansatzes:
1. Sei ein RB-Raum gegeben, so projiziere den Lösungsalgorithmus des inversen Problems auf diesen RB-Raum.
2. Generiere mit Hilfe dieses projizierten Verfahrens neue Iterierte bis entweder eine Iterierte das inverse Problem löst oder bis der RB-Raum erweitert werden muss.
3. Im ersten Fall wird das Verfahren beendet, im zweiten Fall wird die zur aktuellen Iterierten gehörige Vorwärtslösung verwendet um den RB-Raum zu verbessern. Danach wird mit dem ersten Schritt fortgefahren.
Es wird also nach und nach ein lokal approximierender RB-Raum konstruiert, indem Parameter für neue Basisvektoren mittels einer projizierten Variante des Lösungsalgorithmus des inversen Problems gefunden werden. Das neuartige Reduzierte Basis Landweber-Verfahren ist das Hauptresultat von Kapitel 1, wobei das Verfahren ausführlich numerisch untersucht und mit dem ursprünglichen Landweber-Verfahren verglichen wird.
In Kapitel 2 dieser Arbeit soll der zuvor entwickelte adaptive Reduzierte Basis Ansatz auf ein komplexes und praxisrelevantes Problem angewandt werden. Insbesondere soll die dadurch entstehende neue Methode mit Hinblick auf Konvergenz theoretisch ausführlich untersucht werden. Daher widmet sich der zweite Teil dieser Arbeit dem Problem der Magnet Resonanz Elektrischen Impedanztomographie (MREIT).
Bei der MREIT handelt es sich um ein Bildgebungsverfahren, welches während der letzten drei Jahrzehnte entwickelt wurde. Dabei wird ein Gegenstand, an welchen Elektroden angeheftet sind, in einen Kernspintomographen gelegt und es ist das Ziel des Verfahrens die elektrische Leitfähigkeit des Gegenstandes zu bestimmen. Die dazu benötigten Daten werden folgendermaßen gewonnen: indem Strom an einer der Elektroden angelegt wird, wird ein Stromfluss erzeugt, welcher wiederum eine Änderung der Magnetflussdichte induziert. Diese kann mit Hilfe des Kernspintomographen gemessen werden, wodurch man einen vollen Satz innerer Daten zur Hand hat, sodass hoch aufgelöste Bilder der elektrischen Leitfähigkeit des Gegenstandes rekonstruiert werden können.
Als Lösungsalgorithmus für dieses praxisrelevante Problem wird der bereits bekannte Harmonische Bz Algorithmus vorgestellt. Das Problem und der Algorithmus werden mit Hinblick auf Konvergenz des Verfahrens untersucht und ein Konvergenzresultat, welches die bestehende Konvergenztheorie hin zu einem approximativen Harmonischen Bz Algorithmus erweitert, wird bewiesen. Dabei hängt das Resultat nicht davon ab welche Art von Approximation an die Vorwärtslösung der entsprechenden PDGL im approximativen Harmonischen Bz Algorithmus verwendet wird solange diese einer Regularitäts- und einer Qualitätsbedingung genügt. Damit folgt das zweite Hauptresultat dieser Arbeit: die numerische Konvergenz des Harmonischen Bz Algorithmus. Es soll dabei hervorgehoben werden, dass Konvergenzresultate im Bereich der inversen Probleme (sofern es sie gibt) meistens die Kenntnis der exakten Vorwärtslösung annehmen, sodass keine numerische Konvergenz des zugehörigen Verfahrens folgt (in einer numerischen Implementation wird stets eine Approximation an die Vorwärtslösung verwendet). Somit ist dieses Konvergenzresultat ein Schritt hin zur numerischen Konvergenz anderer Lösungsverfahren von inversen Problemen.
Da das theoretische Resultat von der Art der Approximation nicht abhängt, erhält man ebenfalls die Konvergenz des neuartigen Reduzierte Basis Harmonischen Bz Algorithmus, welcher die Kombination des in Kapitel 1 entwickelten adaptiven Reduzierte Basis Ansatzes und des Harmonischen Bz Algorithmus ist. In einer kurzen numerischen Untersuchung wird festgestellt, dass dieser Reduzierte Basis Harmonische Bz Algorithmus schneller als der Harmonische Bz Algorithmus ist, wobei die Qualität der Rekonstruktion gleichbleibend ist. Somit funktioniert der entwickelte adaptive Reduzierte Basis Ansatz auch angewandt auf dieses komplexe praxisrelevante inverse Problem der MREIT.
The Republic of Panama currently has 358 recorded species of Trichoptera. Herein we add 25 new country records for Panama. The newly recorded taxa increase Panama’s total known caddisfly fauna to 383 species, distributed among 15 families and 52 genera. These results are part of an ongoing effort to characterize the caddisfly fauna of Panama, and to evaluate that country’s major watersheds (cuencas).
There have been 136 species of microcaddisflies (Trichoptera: Hydroptilidae) recorded from the Republic of Panama. Herein we describe seven new species from the Mount Totumas Cloud Forest and Biological Reserve, in the upper reaches of the Río Chiriquí Viejo watershed (Costatrichia devestiva, C. dietrichi, Metrichia brocha, M. calla, Neotrichia atopa, Ochrotrichia anticheirion, and Rhyacopsyche totuma). These results are part of an ongoing effort to characterize the aquatic insect fauna of Panama, and to evaluate that country’s major watersheds.
Through this survey, four species of aphelinid, one species of encyrtid, and one species of signiphorid wasp (Hymenoptera: Chalcidoidea) were collected and identified as follows: Aphytis japonicus DeBach and Azim, Encarsia berlesei (Howard), Marietta carnesi (Howard), Pteroptrix sp. 2, Arrhenophagus chionaspidis Aurivillius, and Chartocerus subaenus (Förster). Among these, C. subaenus is recorded newly from the Korean parasitoid fauna. Also, three species of aphelinids and one species of signiphorid are newly added as parasitic wasps associated with Pseudaulacaspis cockerelli (Cooley) (Hemiptera: Coccoidea) from Korea. In this paper, the list of parasitoid species of P. cockerelli that occur in Korea is updated and a brief diagnosis and photographs of these species are provided.
The Scarabaeus subgenus Scarabaeolus Balthasar, 1965 (Scarabaeidae: Scarabaeinae: Scarabaeini) is defined and nine new species are described, six from the Republic of South Africa [S. (S.) fragilis sp. n., S. (S.) krugeri sp. n., S. (S.) lizleri sp. n., S. (S.) orientalis sp. n., S. (S.) rugosipennis sp. n., S. (S.) similis sp. n.] and one each from Angola [S. (S.) cunene sp. n.], Namibia [S. (S.) namibensis sp. n.] and Kenya [S. (S.) werneri sp. n.], bringing the number of recorded species up to 41. Species accounts listing original descriptions, subsequent accounts, type localities, type repositories, and geographic distributions are provided for all the species. The status of S. (S.) reichei Waterhouse, 1890 and of S. (S.) bohemani Harold, 1868, both formerly synonymized and reinstated, are discussed. It is concluded that S. (S.) reichei is synonymous with S. (S.) canaliculatus Fairmaire, 1888, whereas S. (S.) bohemani differs from S. (S.) palemo Olivier, 1789 in the color of antennal club and shape of paramere tips, and is upheld pending availability of molecular data.
Allogeneic hematopoietic stem cell transplantation (allo-HSCT) offers potential cure to acute myeloid leukemia (AML) patients. However, infections with commensal bacteria are an important cause for non-relapse mortality (NRM). We have previously described the impact of multidrug-resistant organism (MDRO) colonization on the survival of allo-HSCT patients. In the aforementioned publication, according to consensus, we there did not consider the opportunistic gram-negative bacterium Stenotrophomonas maltophilia (S. maltophilia) to be an MDRO. Since rate of S. maltophilia colonization is increasing, and it is not known whether this poses a risk for allo-HSCT patients, we here analyzed here its effect on the previously described and now extended patient cohort. We report on 291 AML patients undergoing allo-HSCT. Twenty of 291 patients (6.9%) were colonized with S. maltophilia. Colonized patients did not differ from non-colonized patients with respect to their age, remission status before allo-HSCT, donor type and HSCT-comorbidity index. S. maltophilia colonized patients had a worse overall survival (OS) from 6 months up to 60 months (85% vs. 88.1% and 24.7% vs. 59.7%; p = 0.007) due to a higher NRM after allo-HSCT (6 months: 15% vs. 4.8% and 60 months: 40.1% vs. 16.2% p = 0.003). The main cause of mortality in colonized patients was infection (46.2% of all deaths) and in non-colonized patients relapse (58.8% of all deaths). 5/20 colonized patients developed an invasive infection with S. maltophilia. The worse OS after allo-HSCT due to higher infection related mortality might implicate the screening of allo-HSCT patients for S. maltophilia and a closer observation of colonized patients as outpatients.
Background: Drugs used to treat gastrointestinal diseases (GI drugs) are widely used either as prescription or over23 the-counter (OTC) medications and belong to both the ten most prescribed and ten most sold OTC medications worldwide. Current clinical practice shows that in many cases, these drugs are administered concomitantly with other drug products. Due to their metabolic properties and mechanisms of action, the drugs used to treat gastrointestinal diseases can change the pharmacokinetics of some co27 administered drugs. In certain cases, these interactions can lead to failure of treatment or to the occurrence of serious adverse events. The mechanism of interaction depends highly on drug properties and differs among therapeutic categories. Understanding these interactions is essential to providing recommendations for optimal drug therapy.
Objective: To discuss the most frequent interactions between GI and other drugs, including identification of the mechanisms behind these interactions, where possible.
Conclusion: Interactions with GI drugs are numerous and can be highly significant clinically. Whilst alterations in bioavailability due to changes in solubility, dissolution rate and metabolic interactions can be (for the most part) easily identified, interactions that are mediated through other mechanisms, such as permeability or microbiota, are less well understood. Future work should focus on characterizing these aspects.
Nukleinsäuren besitzen neben der Speicherung und Übertragung der genetischen Information weitere vielfältige Funktionen in einem komplexen und dynamischen Netzwerk von gleichzeitig ablaufenden Prozessen in der Zelle. Die gezielte Kontrolle bestimmter Nukleinsäuren kann helfen, die jeweiligen Prozesse zu studieren oder auch zu manipulieren. Photoaktive Verbindungen, wie photolabile Schutzgruppen oder Photoschalter, sind ideal dazu geeignet die Struktur und Funktion von Nukleinsäuren zu studieren. Photolabile Schutzgruppen werden dazu meistens auf die Nukleobase installiert und stören die Watson-Crick Basenpaarung. Dies verhindert die Ausbildung einer Sekundärstruktur oder die Möglichkeit einen stabilen Doppelstrang zu bilden. Licht ist ein nicht-invasives Trigger-signal und kann mit hoher Orts- und Zeitauflösung angewendet werden, um selektiv die temporär geschützten Nukleinsäuren in der Zelle zu aktivieren.
Das erste Projekt dieser Arbeit ist eine Kooperation mit der Arbeitsgruppe von Prof. Erin Schuman (MPI für Hirnforschung) und beschäftigt sich mit der lichtgesteuerten Regulation der miR-181a Aktivität in hippocampalen Neuronen von Ratten. Die Langzeitpotenzierung (LTP) ist der primäre Mechanismus von synaptischer Plastizität und somit essentiell für Lernen und Gedächtnis. Die langfristige Aufrechterhaltung von LTP erfordert eine gesteigerte (lokale) Proteinbiosynthese, ein Prozess, der noch nicht vollständig aufgeklärt ist. Die miR-181a reguliert die Genexpression von zwei für synaptische Plastizität wichtigen Proteinen, GluA2 und CaMKIIα. Mit einem lichtaktivierbaren AntimiR sollte der Einfluss der miR-181a auf die lokale Proteinsynthese von CaMKIIα und GluA2 untersucht werden. Photolabile Schutzgruppen sollen eine ortsaufgelöste Aktivierung des AntimiRs in den Dendriten ermöglichen. Ein Tracking-Fluorophor sollte die Lokalisierung des AntimiRs und eine gezielte Lichtaktivierung ermöglichen. Die Bindung der miRNA sollte fluoreszent visualisiert werden können, um eine Korrelation zwischen der inhibierten Menge an miR-181a und den neu synthetisierten CaMKIIα-Molekülen zu untersuchen. In diesem Projekt wurden drei Konzepte zur Synthese von lichtregulierbaren AntimiR-Sonden verglichen: Das erste Konzept verwendete eine Thiazolorange-basierte Hybridisierungssonde nach Seitz et al. Allerdings war mit diesem Konzept der Fluoreszenzanstieg zur Visualisierung der Hybridisierung zu gering. Im zweiten Konzept wurde ein dual-Fluorophor markierter Molecular Beacon entwickelt, bei dem die photolabilen Schutzgruppen in der Schleifen-Region die Hybridisierung der miR-181a vor Belichtung verhinderten. Nach Optimierung der Stammlänge, Anzahl und Position der photolabilen Schutzgruppen, sowie Auswahl des idealen Fluorophor-Quencher Paars, konnte nach UV-Bestrahlung in Anwesenheit der miR-181a ein signifikanter Anstieg des Hybridisierungsreporter-Fluorophors gemessen werden. Das dritte Konzept untersuchte lichtaktivierbare Hairpin-Sonden, bei denen ein Gegenstrang (Blockierstrang) über einen photospaltbaren Linker mit dem AntimiR verknüpft wurde. Dabei musste die optimale Länge des Blockierstrangs und die Anzahl der photo-spaltbaren Linker im Blockierstrang ermittelt werden, sodass die miR-181a erst nach Photoaktivierung das AntimiR binden und den Quencher-markierten Strang verdrängen konnte. Die in vitro Experimente vom Arbeitskreis Schuman waren zu dem Zeitpunkt des Einreichens dieser Arbeit noch nicht abgeschlossen. Erste Ergebnisse zeigten, dass der mRNA und Protein-Level von CaMKIIα eines gesamten hippocampalen Neurons durch ein nicht-lichtaktivierbare AntimiR um den Faktor ~1,5 gesteigert werden konnte. Zudem konnte durch die lokale Bestrahlung einer lichtaktivierbaren Hairpin-Sonde die lokale Gen-expression von CaMKIIα in einem Dendriten deutlich gesteigert werden.
Das zweite Projekt dieser Arbeit beschäftigte sich mit der reversiblen Lichtregulation von DNA und RNA durch Azobenzol Photoschalter. Azobenzole eignen sich ideal für die Regulation der Duplexstabilität, denn das planare trans-Azobenzol kann zwischen die Basen interkalieren und somit einen Doppelstrang stabilisieren. UV-Licht überführt das trans-Isomer in das cis-Isomer. Dies ist gewinkelt, benötigt mehr Platz und stört dadurch die Stabilität eines Nukleinsäuredoppelstrangs. Entscheidend für die Effizienz der Regulation der Duplexstabilität ist der Linker, der das Azobenzol mit der Nukleinsäure verknüpft. Während vorangegange Studien von Asanuma et al. unnatürliche Linker (D-Threoninol, tAzo) verwendeten, wurde in dieser Studie das Azobenzol mit der C1‘-Position von (Desoxy-)Ribose C-Nukleoside verknüpft, um Azobenzol (pAzo und mAzo) zu erhalten. Der Riboselinker sollte die helikale Natur der Nukleinsäure optimal nachahmen und möglichst wenig Störung des Ribose-Phosphat-Rückgrats bewirken. Thermische Stabilitätsstudien zeigten, dass UV-Licht induzierte trans-zu-cis Isomerisierung den Schmelzpunkt eines RNA- und DNA-Duplexes um 5,9 und 4,6 °C erniedrigte. Dabei führte der Austausch eines Nukleotids gegen pAzo oder mAzo zu einer effektiveren Regulation der Duplexstabilität als der zusätzliche Einbau eines Azobenzol C-Nukleosids in die Sequenz. Ein Vergleich mit dem in der Literatur etablierten System, tAzo, zeigte, dass pAzo und mAzo teilweise einen stärkeren Duplexdestabilisierungseffekt nach UV-Bestrahlung bewirkten.
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While interleukin (IL)-1β is a potent pro-inflammatory cytokine involved in host defense, high levels can cause life-threatening sterile inflammation including systemic inflammatory response syndrome. Hence, the control of IL-1β secretion is of outstanding biomedical importance. In response to a first inflammatory stimulus such as lipopolysaccharide, pro-IL-1β is synthesized as a cytoplasmic inactive pro-form. Extracellular ATP originating from injured cells is a prototypical second signal for inflammasome-dependent maturation and release of IL-1β. The human anti-protease alpha-1 antitrypsin (AAT) and IL-1β regulate each other via mechanisms that are only partially understood. Here, we demonstrate that physiological concentrations of AAT efficiently inhibit ATP-induced release of IL-1β from primary human blood mononuclear cells, monocytic U937 cells, and rat lung tissue, whereas ATP-independent IL-1β release is not impaired. Both, native and oxidized AAT are active, suggesting that the inhibition of IL-1β release is independent of the anti-elastase activity of AAT. Signaling of AAT in monocytic cells involves the lipid scavenger receptor CD36, calcium-independent phospholipase A2β, and the release of a small soluble mediator. This mediator leads to the activation of nicotinic acetylcholine receptors, which efficiently inhibit ATP-induced P2X7 receptor activation and inflammasome assembly. We suggest that AAT controls ATP-induced IL-1β release from human mononuclear blood cells by a novel triple-membrane-passing signaling pathway. This pathway may have clinical implications for the prevention of sterile pulmonary and systemic inflammation.
Personen- und Organisationsmerkmale als Gelingensbedingungen im pädagogischen Vorbereitungsdienst
(2018)
Die vorliegende Arbeit greift die defizitäre empirische Befundlage zur Wahrnehmung der zweiten Ausbildungsphase des Lehrerberufs – dem Referendariat – auf. Sie geht der Frage nach, wie das Belastungserleben der Referendare mit Merkmalen der Person oder Organisation verknüpft ist. Bestehende Forschungsaktivtäten legen ihren Fokus auf die Wahrnehmung erfahrener Lehrkräfte im Beruf. Es fehlt an Studien, die das Erleben im Referendariat diskutieren. Die vorliegende, primär explorativ ausgerichtete Arbeit nimmt diese Ausbildungsphase in den Blick. Die Datenbasis der Arbeit bildet die Evaluationsstudie „Pädagogische Entwicklungsbilanzen an Studienseminaren“ (PEB-Sem), die in Hessen zum Einsatz kam. Es werden Daten von 3808 Referendaren sekundäranalytisch ausgewertet. Da die Beschreibung der Untersuchungsgruppe im Referendariat selbst wenig Vergleichsmöglichkeiten zur Absicherung der Daten bietet, wurde PEB-Sem im Praxissemester bei einer Vergleichsgruppe von Lehramtsstudierenden an der Goethe-Universität eingesetzt.
Personale Merkmale im Umgang mit Belastungen wurden über objektive Aspekte (Alter, Geschlecht, Lehramtsstufe, pädagogische Vorerfahrungen) sowie über Persönlichkeitscharakteristika (Selbstwirksamkeitserwartungen, Resilienz) operationalisiert. Merkmale der Organisation des Vorbereitungsdiensts wurden über Skalen erhoben, welche die Ausbildungsbeziehungen zwischen Referendaren und Ausbildern, Mentoren sowie der Seminarleitung oder die Kohärenz der Ausbildung erfassen.
In den Ergebnissen der Analyse personenbezogener Merkmale zeigt sich, dass vor allem die Resilienz das Belastungserleben der Referendare erklären kann, während die pädagogischen Vorerfahrungen oder die Selbstwirksamkeitserwartungen nur einen geringen Anteil der Belastungswahrnehmung erklären können. Die Belastung in der Ausbildung wird über die Zentralstellung des Leistungsdrucks, der durch die bewerteten Unterrichtsbesuche, Zeitdruck oder auch die Prüfungsbelastung zum Ende der Ausbildung entsteht, maßgeblich bestimmt. Zwischen den Faktoren der Organisation und der Belastungswahrnehmung, wie sie z.B. für die Unterstützung durch die Ausbilder und Mentoren untersucht wurden, konnten nur schwache Zusammenhänge zur Belastung nachgewiesen werden. Die vergleichende Betrachtung von Referendaren und Studierenden im Praxissemester kann Unterschiede im Erleben dieser beiden Ausbildungsabschnitte herausarbeiten. Die berufliche Erfahrung, welche die Referendare den Studierenden voraushaben, wirkt sich, entgegen der Annahme, nicht positiv auf die Belastungswahrnehmung aus: Referendare zeigen sich stärker belastet als Lehramtsstudierende. Bezogen auf die Unterschiede in der Einschätzung der Resilienz sind es wieder die Lehramtsstudierenden, die im Vergleich zu den Referendaren über eine stärkere Widerstandfähigkeit verfügen.
Die vergleichende Betrachtung beider Ausbildungsphasen vermitteln ein besseres Verständnis und eine größere Nähe zum jeweiligen Ausbildungskontext. Die Befunde der Studie deuten auf die Notwendigkeit hin, sich mit Unsicherheiten und Belastungen, die durch die Bewertungssituationen und den Anpassungsdruck an die Erwartungen der Ausbilder und Mentoren entstehen können, stärker zu befassen. An diese Ergebnisse lassen sich Implikationen für die Praxis und mögliche Ansatzpunkte für weitere Forschungsbemühen anschließen.
Bacterial pathogens exploit eukaryotic pathways for their own end. Upon ingestion, Salmonella enterica serovar Typhimurium passes through the stomach and then catalyzes its uptake across the intestinal epithelium. It survives and replicates in an acidic vacuole through the action of virulence factors secreted by a type three secretion system located on Salmonella pathogenicity island 2 (SPI-2). Two secreted effectors, SifA and SseJ, are sufficient for endosomal tubule formation, which modifies the vacuole and enables Salmonella to replicate within it. Two-color, superresolution imaging of the secreted virulence factor SseJ and tubulin revealed that SseJ formed clusters of conserved size at regular, periodic intervals in the host cytoplasm. Analysis of SseJ clustering indicated the presence of a pearling effect, which is a force-driven, osmotically sensitive process. The pearling transition is an instability driven by membranes under tension; it is induced by hypotonic or hypertonic buffer exchange and leads to the formation of beadlike structures of similar size and regular spacing. Reducing the osmolality of the fixation conditions using glutaraldehyde enabled visualization of continuous and intact tubules. Correlation analysis revealed that SseJ was colocalized with the motor protein kinesin. Tubulation of the endoplasmic reticulum is driven by microtubule motors, and in the present work, we describe how Salmonella has coopted the microtubule motor kinesin to drive the force-dependent process of endosomal tubulation. Thus, endosomal tubule formation is a force-driven process catalyzed by Salmonella virulence factors secreted into the host cytoplasm during infection.
Truffles (Tuber spp.) are the fruiting bodies of symbiotic fungi, which are prized food delicacies. The marked aroma variability observed among truffles of the same species has been attributed to a series of factors that are still debated. This is because factors (i.e. genetics, maturation, geographical location and the microbial community colonizing truffles) often co-vary in truffle orchards. Here, we removed the co-variance effect by investigating truffle flavour in axenic cultures of nine strains of the white truffle Tuber borchii. This allowed us to investigate the influence of genetics on truffle aroma. Specifically, we quantified aroma variability and explored whether strain selection could be used to improve human-sensed truffle flavour. Our results illustrate that aroma variability among strains is predominantly linked to amino acid catabolism through the Ehrlich pathway, as confirmed by 13C labelling experiments. We furthermore exemplified through sensory analysis that the human nose is able to distinguish among strains and that sulfur volatiles derived from the catabolism of methionine have the strongest influence on aroma characteristics. Overall, our results demonstrate that genetics influences truffle aroma much more deeply than previously thought and illustrate the usefulness of strain selection for improving truffle flavour.
Regulation of protein turnover allows cells to react to their environment and maintain homeostasis. Proteins can show different turnover rates in different tissue, but little is known about protein turnover in different brain cell types. We used dynamic SILAC to determine half-lives of over 5100 proteins in rat primary hippocampal cultures as well as in neuron-enriched and glia-enriched cultures ranging from <1 to >20 days. In contrast to synaptic proteins, membrane proteins were relatively shorter-lived and mitochondrial proteins were longer-lived compared to the population. Half-lives also correlate with protein functions and the dynamics of the complexes they are incorporated in. Proteins in glia possessed shorter half-lives than the same proteins in neurons. The presence of glia sped up or slowed down the turnover of neuronal proteins. Our results demonstrate that both the cell-type of origin as well as the nature of the extracellular environment have potent influences on protein turnover.
Many cancers have the tumor suppressor p53 inactivated by mutation, making reactivation of mutant p53 with small molecules a promising strategy for the development of novel anticancer therapeutics. The oncogenic p53 mutation Y220C, which accounts for approximately 100,000 cancer cases per year, creates an extended surface crevice in the DNA-binding domain, which destabilizes p53 and causes denaturation and aggregation. Here, we describe the structure-guided design of a novel class of small-molecule Y220C stabilizers and the challenging synthetic routes developed in the process. The synthesized chemical probe MB710, an aminobenzothiazole derivative, binds tightly to the Y220C pocket and stabilizes p53-Y220C in vitro. MB725, an ethylamide analogue of MB710, induced selective viability reduction in several p53-Y220C cancer cell lines while being well tolerated in control cell lines. Reduction of viability correlated with increased and selective transcription of p53 target genes such as BTG2, p21, PUMA, FAS, TNF, and TNFRSF10B, which promote apoptosis and cell cycle arrest, suggesting compound-mediated transcriptional activation of the Y220C mutant. Our data provide a framework for the development of a class of potent, non-toxic compounds for reactivating the Y220C mutant in anticancer therapy.
In 1957, Craig Mooney published a set of human face stimuli to study perceptual closure: the formation of a coherent percept on the basis of minimal visual information. Images of this type, now known as “Mooney faces”, are widely used in cognitive psychology and neuroscience because they offer a means of inducing variable perception with constant visuo-spatial characteristics (they are often not perceived as faces if viewed upside down). Mooney’s original set of 40 stimuli has been employed in several studies. However, it is often necessary to use a much larger stimulus set. We created a new set of over 500 Mooney faces and tested them on a cohort of human observers. We present the results of our tests here, and make the stimuli freely available via the internet. Our test results can be used to select subsets of the stimuli that are most suited for a given experimental purpose.
Effect of progesterone on Smad signaling and TGF-β/Smad-regulated genes in lung epithelial cells
(2018)
The effect of endogenous progesterone and/or exogenous pre- or postnatal progesterone application on lung function of preterm infants is poorly defined. While prenatal progesterone substitution may prevent preterm birth, in vitro and in vivo data suggest a benefit of postnatal progesterone replacement on the incidence and severity of bronchopulmonary dysplasia (BPD). However, the molecular mechanisms responsible for progesterone’s effects are undefined. Numerous factors are involved in lung development, airway inflammation, and airway remodeling: the transforming growth factor beta (TGF-β)/mothers against decapentaplegic homolog (Smad) signaling pathway and TGF-β-regulated genes, such as connective tissue growth factor (CTGF), transgelin (TAGLN), and plasminogen activator inhibitor-1 (PAI-1). These processes contribute to the development of BPD. The aim of the present study was to clarify whether progesterone could affect TGF-β1-activated Smad signaling and CTGF/transgelin/PAI-1 expression in lung epithelial cells. The pharmacological effect of progesterone on Smad signaling was investigated using a TGF-β1-inducible luciferase reporter and western blotting analysis of phosphorylated Smad2/3 in A549 lung epithelial cells. The regulation of CTGF, transgelin, and PAI-1 expression by progesterone was studied using a promoter-based luciferase reporter, quantitative real-time PCR, and western blotting in the same cell line. While progesterone alone had no direct effect on Smad signaling in lung epithelial cells, it dose-dependently inhibited TGF-β1-induced Smad3 phosphorylation, as shown by luciferase assays and western blotting analysis. Progesterone also antagonized the TGF-β1/Smad-induced upregulation of CTGF, transgelin, and PAI-1 at the promoter, mRNA, and/or protein levels. The present study highlights possible new molecular mechanisms involving progesterone, including inhibition of TGF-β1-activated Smad signaling and TGF-β1-regulated genes involved in BPD pathogenesis, which are likely to attenuate the development of BPD by inhibiting TGF-β1-mediated airway remodeling. Understanding these mechanisms might help to explain the effects of pre- or postnatal application of progesterone on lung diseases of preterm infants.
This study was designed to characterize morphologic stages during neuroma development post amputation with an eye toward developing better treatment strategies that intervene before neuromas are fully formed. Right forelimbs of 30 Sprague Dawley rats were amputated and limb stumps were collected at 3, 7, 28, 60 and 90 Days Post Amputation (DPA). Morphology of newly formed nerves and neuromas were assessed via general histology and neurofilament protein antibody staining. Analysis revealed six morphological characteristics during nerve and neuroma development; 1) normal nerve, 2) degenerating axons, 3) axonal sprouts, 4) unorganized bundles of axons, 5) unorganized axon growth into muscles, and 6) unorganized axon growth into fibrotic tissue (neuroma). At early stages (3 & 7 DPA) after amputation, normal nerves could be identified throughout the limb stump and small areas of axonal sprouts were present near the site of injury. Signs of degenerating axons were evident from 7 to 90 DPA. From day 28 on, variability of nerve characteristics with signs of unorganized axon growth into muscle and fibrotic tissue and neuroma formation became visible in multiple areas of stump tissue. These pathological features became more evident on days 60 and 90. At 90 DPA frank neuroma formation was present in all stump tissue. By following nerve regrowth and neuroma formation after amputation we were able to identify 6 separate histological stages of nerve regrowth and neuroma development. Axonal regrowth was observed as early as 3 DPA and signs of unorganized axonal growth and neuroma formation were evident by 28 DPA. Based on these observations we speculate that neuroma treatment and or prevention strategies might be more successful if targeted at the initial stages of development and not after 28 DPA.
Background and aims: Expression of carbonic anhydrase IX (CA9), an enzyme expressed in response to hypoxia, acidosis and oncogenic alterations, is reported to be a prognostic factor in HCC patients. Here we evaluated serum CA9 levels in HCC and cirrhosis patients.
Methods: HCC and cirrhosis patients were prospectively recruited and CA9 levels were determined. CA9 levels were compared to stages of cirrhosis and HCC stages. The association of the CA9 levels and overall survival (OS) was assessed. Furthermore, immunohistochemical CA9 expression in HCC and cirrhosis was evaluated.
Results: 215 patients with HCC were included. The median serum CA9 concentration in patients with HCC was 370 pg/ml and significantly higher than in a healthy cohort. Patients with advanced cancer stages (BCLC and ALBI score) had hid significant higher levels of CA9 in the serum. HCC patients with high serum CA9 concentrations (>400 pg/ml) had an increased mortality risk (hazard ratio (HR) 1.690, 95% confidence interval (CI) 1.017–2.809, P = 0.043). Serum CA9 concentration in cirrhotic patients did not differ significantly from HCC patients. Higher CA9 levels in cirrhotic patients correlated with portal hypertension and esophageal varices. Patients with ethanol induced cirrhosis had the highest CA9 levels in both cohorts. Levels of CA9 did not correlate with immunohistochemical expression.
Conclusions: We conclude that a high CA9 level is a possible prognostic indicator for a poor outcome in HCC patients. The high CA9 levels are probably mainly associated with portal hypertension. Ductular reactions might be a possible source of serum CA9.
Transmission of temporally correlated spike trains through synapses with short-term depression
(2018)
Short-term synaptic depression, caused by depletion of releasable neurotransmitter, modulates the strength of neuronal connections in a history-dependent manner. Quantifying the statistics of synaptic transmission requires stochastic models that link probabilistic neurotransmitter release with presynaptic spike-train statistics. Common approaches are to model the presynaptic spike train as either regular or a memory-less Poisson process: few analytical results are available that describe depressing synapses when the afferent spike train has more complex, temporally correlated statistics such as bursts. Here we present a series of analytical results—from vesicle release-site occupancy statistics, via neurotransmitter release, to the post-synaptic voltage mean and variance—for depressing synapses driven by correlated presynaptic spike trains. The class of presynaptic drive considered is that fully characterised by the inter-spike-interval distribution and encompasses a broad range of models used for neuronal circuit and network analyses, such as integrate-and-fire models with a complete post-spike reset and receiving sufficiently short-time correlated drive. We further demonstrate that the derived post-synaptic voltage mean and variance allow for a simple and accurate approximation of the firing rate of the post-synaptic neuron, using the exponential integrate-and-fire model as an example. These results extend the level of biological detail included in models of synaptic transmission and will allow for the incorporation of more complex and physiologically relevant firing patterns into future studies of neuronal networks.
Im Zeitraum vom 7. bis zum 9. Dezember 2017 fand an der Universität Breslau (Wrocław) in Kooperation mit der Ruhr-Universität Bochum die Winterschool "Europa: Poetik und Politik" statt. Die gut zwanzig Teilnehmerinnen und Teilnehmer – darunter Professor*innen, wissenschaftliche Mitarbeiter*innen und Studierende beider Universitäten – diskutierten die neuere Geschichte von Europa-Diskursen von der Romantik bis in die Gegenwart. Ausgangspunkt der Tagung war die gegenwärtige Krise der Europäischen Union, die – so zeigte sich im Verlauf der Tagung – als Fortführung der leitmotivischen 'Schwellensituationen' zu verstehen ist, die als das Gemeinsame der diskutierten Texte und somit in gewisser Weise als konstitutiv für den Europa-Diskurs erkannt wurden.
Entwicklung von Immunisierungsstrategien zur Induktion hoher funktionaler Antikörperantworten
(2018)
Neuartige Viren und Erreger, die sich antigenetisch tiefgreifend von bekannten Varianten unterscheiden, können verheerende Epidemien auslösen, da weder gegen diese Erreger eine Immunität in der Bevölkerung besteht, noch prophylaktische oder therapeutische Maßnahmen verfügbar sind. Eine prophylaktisch vermittelte Immunität durch Impfung stellt die bei Weitem effektivste Methode zur Vorbeugung viraler Infektionen dar, jedoch sind die Entwicklungs- und Herstellungszeiten eines neuen Impfstoffs in der Regel mit der Ausbruchsdynamik nicht kompatibel. Inzwischen steht zwar eine überschaubare Anzahl antiviraler Medikamente zur Verfügung, doch ist die Wahrscheinlichkeit gering, dass diese meist hoch spezifischen Wirkstoffe gegen neu auftretende Viren aktiv sind. Das beispiellose Ausmaß der Ebola-Epidemie 2014 führte zum Einsatz experimenteller antikörperbasierter Therapien, welche das Potential der passiven Vermittlung von temporärem Immunschutz naiver Personen verdeutlicht. Für viele neuartige Viren ist die Entwicklung von Therapieansätzen allerdings noch nicht entsprechend weit fortgeschritten. Zudem bedingt eine Verwendung des eigentlichen Erregers oft hohe Sicherheitsmaßnahmen, was die Arbeit erschwert. Aus diesem Grund werden Notfalltherapien benötigt, die schnell in klinisch relevanter Qualität und Quantität unter niedrigen biologischen Sicherheitsmaßnahmen produziert werden können.
Diese Arbeit basiert auf der zentralen Hypothese, dass die Induktion von hohen Titern funktioneller Antikörperantworten die Basis für einen breiteren Schutz gegen antigenetisch entferntere Virusstämme sowie für die schnelle Produktion von therapeutischen Antiseren darstellt.
Um diese Hypothese zu testen und Einblicke in verschiedene Aspekte dieses Prozesses zu bekommen, wurde zunächst die Nutzung von Adjuvanzien als Zusätze für Impfstoffe am Beispiel des pandemischen A(H1N1)pdm09-Impfstoffs untersucht. Neben den alljährlichen Epidemien, die von saisonalen Influenza-A-Viren der Subtypen H1N1 oder H2N3 verursacht werden, können neuartige Subtypen zu weltweiten Pandemien führen. Während die saisonalen Influenza-Impfstoffe in der Regel keine Adjuvanzien enthalten, wurden einige pandemische H1N1-Impfstoffe aus 2009 mit einem reduzierten Antigengehalt formuliert und mit squalenbasierten Adjuvanzien kombiniert, um eine ausreichende Wirksamkeit bei größerer Verfügbarkeit zu gewährleisten. Zur Charakterisierung des Effekts dieser Adjuvanzien auf die Immunantworten wurden Frettchen mit 2 µg des kommerziellen H1N1pmd09-Impfstoffes alleine sowie in Kombination mit verschiedenen Adjuvanzien immunisiert, die Antikörpertiter gegen homologe und heterologe Influenzastämme untersucht und mit dem Schutz vor einer Infektion korreliert. Dabei zeigte sich, dass die Verwendung squalenbasierter Adjuvanzien die funktionalen Antikörperantworten um das 100-fache erhöhte und zu einer signifikant reduzierten Viruslast nach der Infektion mit dem homologen pandemischen Virus führte. Während in keiner Gruppe Antikörper gegen die heterologen Hämagglutinin-(HA-)Proteine H3, H5, H7 und H9 nachweisbar waren, induzierten mit squalenbasierten Adjuvanzien kombinierte Impfstoffe subtypenspezifische Antikörper gegen das N1 Neuraminidase-(NA-)Protein einschließlich H5N1. Darüber hinaus führte die Immunisierung mit squalenbasierten Adjuvanzien zu einer besseren Kontrolle der Influenzavirus-Replikation in den oberen Atemwegen.
Anschließend wurde im zweiten Teil dieser Arbeit unter Einbeziehung der gewonnenen Erkenntnisse eine Immunisierungsstrategie zur schnellen Produktion therapeutischer Hyper-immunseren entwickelt, wobei unterschiedliche Antigenexpressionssysteme miteinander verglichen wurden. Während in den frühen Stadien eines Ausbruchs Rekonvaleszenzseren nicht ohne weiteres verfügbar sind, können Antiseren tierischen Ursprungs innerhalb eines kurzen Zeitraums hergestellt werden. Die Herausforderung liegt in der schnellen Induktion einer schützenden Immunität, wobei die effiziente Produktion und Reinigung von Hyperimmunserum in klinisch relevanten Mengen ebenso essenziell ist wie die Anpassungsfähigkeit der Immunisierungsstrategie an neue oder hinsichtlich ihrer Antigenizität veränderte Viren. Hierzu wurden verschiedene Immunisierungsstrategien in Mäusen und Kaninchen verglichen, die unterschiedliche Expressionssysteme für das Modellantigen Ebolavirus-Glykoprotein (EBOV-GP) verwenden: (i) Ebolavirus-ähnliche Partikel (VLP), (ii) das rekombinante modifizierte Vacciniavirus Ankara (MVA) sowie (iii) das rekombinante Virus der vesikulären Stomatitis (VSV). Im Ergebnis induzierte eine dreimalige Immunisierung mit VLPs in Kombination mit squalenhaltigem Adjuvans neutralisierende Antikörpertiter, die vergleichbar mit der Immunisierung mit replikationskompetentem VSVΔG/EBOV-GP waren. Dies deutet darauf hin, dass nicht die De-novo-Antigenexpression, sondern vielmehr die mehrfache Präsentation des Antigens in nativer Konformation für die Produktion von neutralisierenden Antikörpern essenziell ist. Darüber hinaus waren die funktionalen Antikörpertiter aller Kaninchenseren in der In-vitro-Analyse gegen das Wildtypvirus 10- bis 100-fach höher als der Durchschnitt, der in mit VSVΔG/EBOV-GP geimpften Probanden beobachtet wurde. Die Etablierung eines optimierten mehrstufigen Reinigungsverfahrens unter Verwendung einer zweistufigen Ammoniumsulfat-Präzipitation, gefolgt von einer Protein-A-Affinitätschromatographie, führte zu aufgereinigten IgG-Präparationen mit nahezu unveränderter neutralisierender Aktivität, die über neun Tage im xenogenen In-vivo-Modell stabil waren. Die signifikante Erhöhung von totalen und funktionalen Antikörpertitern in Kombination mit einer größeren Breite der Antikörperantwort im Kontext von squalenbasierten Adjuvanzien stützt die Hypothese dieser Arbeit. Adjuvantierte Immunisierungsstrategien sind damit ein vielversprechender Ansatz nicht nur zur Wirksamkeitssteigerung von Subunit- und Proteinimpfstoffen, sondern auch zur schnellen Herstellung von therapeutischen Antiseren.
Um molekulare Mechanismen in biologischen Prozessen zu verstehen, ist es unerlässlich biologisch aktive Verbindungen zu kontrollieren. Dabei spielt besonders die Aktivierung bzw. Desaktivierung von Genabschnitten eine zentrale Rolle in der gegenwärtigen chemischen, biologischen und medizinischen Forschung. Nukleinsäuren sind dabei offenkundige Zielmoleküle, da sie die Genexpression auf unterster Ebene regulieren und auf vielfältige Art und Weise an biologischen Prozessen beteiligt sind. Um solch eine genaue Steuerung zu erreichen, werden Nukleinsäuren häufig photolabil modifiziert und unter die Kontrolle von Licht gebracht. Da hochentwickelte Technologien es erlauben Photonen bestimmter Energie unter präziser räumlicher und zeitlicher Auflösung zu dosieren, ist Licht als nicht invasives Triggersignal ein besonders geeignetes Werkzeug um molekulare Prozesse zu kontrollieren.
Die Verwendung photolabiler Schutzgruppen („cage“) ermöglicht es, diese lichtaktivierbaren Nukleinsäuren („caged compound“) herzustellen. Üblicherweise werden Oligonukleotide damit an funktionsbestimmenden Stellen versehen, woraufhin die Funktion der Oligonukleotide unterdrückt wird. Die biologische Aktivität kann durch Bestrahlung mit Licht wieder hergestellt werden, da die photolabile Schutzgruppe durch den Lichtimpuls abgespalten wird. Neben der zeitweiligen Maskierung der Nukleinsäureaktivität existiert auch eine Methode, die als „photoaktivierbarer Strangbruch“ (‘‘caged strand break‘‘) bezeichnet wird. Dabei werden mit Hilfe von photolabilen Linkern (‘‘Verknüpfer‘‘) lichtinduzierte Strangbrüche in Oligonukleotiden ausgelöst, um so beispielsweise die Struktur eines Nukleinsäurestrangs zu zerstören. Die Idee der photoaktivierbaren Strangbrüche ist nicht neu, dennoch werden photolabile Schutzgruppen überwiegend nach der erstgenannten Strategie verwendet. Im Rahmen dieses Promotionsvorhabens wurden neue photosensitive Linkerbausteine für Oligonukleotide entwickelt und hergestellt, welche sich vor allem im Hinblick auf die Anwendbarkeit in lebenden biologischen Systemen von den bisherigen photolabilen Linkern unterscheiden.
Im ersten Projekt wurde ein nicht-nukleosidischer, photolabiler Linker, basierend auf dem Cumaringrundgerüst, entwickelt. Das Ziel war hier, vor allem, einen zweiphotonenaktiven Linker für biologische Anwendungen und Zweiphotonen-Fragestellungen nutzbar zu machen. Bisherige Zweiphotonen-Linker konnten hauptsächlich nur für Proteinverknüpfungen bzw. Neurotransmitter verwendet werden oder mussten chemisch umständlich (z.B. Click-Chemie) und postsynthetisch in Oligonukleotide eingeführt werden. Der neu entwickelte Zweiphotonen-Linker wurde als Phosphoramiditbaustein für die Oligonukelotid-Festphasensynthese synthetisiert, was einen problemlosen und automatisierten Einbau garantiert. Mit einem modifizierten Oligonukleotid konnten die photochemischen Eigenschaften des Linkers bestimmt und mit Hilfe eines fluoreszenzbasierten Verdrängungsassays und Lasertechniken der Zweiphotonen-Effekt visualisiert werden. Dazu wurde ein Hairpin-DNA-Strang hergestellt, welcher eine Linkermodifikation im Bereich der Loopregion enthält. Durch eine Thiolmodifikation am 5‘-Ende des Oligonukleotidstranges war es möglich, diesen in einem Maleimid-funktionalisierten Hydrogel zu fixieren. Ein DNA-Duplex mit einem Fluorophor/Quencherpaar und einer korrespondierenden Sequenz zum modifizierten Hairpin-Strang wurde ebenfalls dem System zugegeben, allerdings wurde dieser nicht fixiert, um Diffusion zu ermöglichen. Durch die räumliche Nähe des Fluorophors zum Quencher konnte im unbelichteten Zustand zunächst keine Fluoreszenz gemessen werden. Mit einem (Femtosekunden-)gepulsten Laser und dem damit verbundenen Bindungsbruch im Hairpin-Strang durch Zweiphotonen-Effekte wurde es dem fluoreszierenden Strang des DNA-Duplex ermöglicht, sich vom Quencher-Strang zu lösen und an den fixierten Strang zu hybridisieren. Das Photolyse-Ereignis konnte so in ein lokales Fluoreszenzsignal übersetzt und detektiert werden.
Der eindeutige Beweis, dass es sich tatsächlich um ein Zweiphotonen-induziertes Ereignis handelt, konnte durch die dreidimensional aufgelöste Photolyse und über die quadratische Anhängigkeit des Fluoreszenzsignals von der eingestrahlten Laserleistung erbracht werden.
Die generelle Kompatibilität des Cumarin-Linkers mit biologischen Systemen konnte in Zellkulturexperimenten gezeigt werden. Dazu wurde eine Transkriptionsfaktor-DNA Decoy-Strategie entwickelt, in der Linker-modifizierte DNA Decoys an regulatorische Transkriptionsfaktoren binden und diese aber auch photochemisch wieder freisetzen können („catch and release-Strategie“). Zellkulturexperimente, um mit dieser Methode das Transkriptionsfaktor-gesteuerte und endogene Gen für Cyclooxygenase-2 (COX2) zu regulieren, lieferten keine aussagekräftigen Ergebnisse. Daher wurden die verwendeten Zellen dahingehend manipuliert, sodass sie das Protein GFP (grün fluoreszierendes Protein) in Abhängigkeit von der Anwesenheit eines Transkriptionsfaktors exprimieren. Das so durch die Zellen verursachte Fluoreszenzsignal steht in direkter Abhängigkeit zur Decoy-Aktivität. Mit Hilfe modifizierter GFP-Decoys konnte hierbei eine Regulation auf Transkriptionsebene in biologischen Organismen erreicht werden. Mit dem Electrophoretic Mobility Shift Assay (EMSA), einer molekularbiologischen in vitro-Analysetechnik, wurden die Interaktionen zwischen modifizierten Decoys und dem Transkriptionsfaktor untersucht.
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This thesis is concerned with systematic investigations of electronic noise in novel condensed matter systems. Although fluctuations are frequently considered a nuisance, that is, a disturbance limiting the accuracy of scientific measurements, in many cases they can reveal fundamental information about the inherent system dynamics. During the past decades, the study of electronic fluctuations has evolved into an indispensable tool in condensed matter physics.
The focus of the present work lies both in a further development of the fluctuation spectroscopy technique and in the study of materials of current interest. In particular, a comprehensive study of the charge carrier dynamics in the archetypal diluted magnetic semiconductors (Ga,Mn)As and (Ga,Mn)P was performed. In spite of extensive research work carried out during the last years, there still exists no theoretical consensus on the precise mechanism of ferromagnetic order and the electronic structure in these materials. Moreover, disorder and correlation effects complicate the understanding of these compounds.
Fluctuation spectroscopy experiments presented in this work provide strong evidence that a percolation transition is observed in samples with localized charge carriers, since the normalized resistance noise magnitude displays a significant enhancement around the Curie temperature. In addition, this quantity exhibits a power law scaling behavior as a function of the resistance, which is in good agreement with theoretical models of percolating systems.
By contrast, it was found that the resistance noise in metallic samples is mainly dominated by the physics of defects such as manganese interstitials and arsenic antisites. Furthermore, first noise studies were carried out on hafnia- and yttria-based resistive random access memories. In these memristor devices, the rupture and re-formation of oxygen deficient conducting filaments caused by the electric field and Joule heating driven motion of mobile anions lead to an unusual resistance switching behavior. For the first time, comparative noise measurements on oxygen deficient and stoichiometric hafnium oxide devices, as well as on novel yttrium oxide based devices were performed in this work. Finally, new strategies for noise measurements of highly insulating and extremely low-resistive samples were developed and realized. In detail, an experimental setup for the measurements of dielectric polarization fluctuations in insulating systems was designed and successfully tested. Here, the polarization noise of a sample is measured as current or voltage fluctuations produced within a capacitance cell. The study of dielectric polarization noise allows for conclusions to be drawn regarding equilibrium structural dynamics in insulators such as relaxor ferroelectrics. On the other hand, as successfully demonstrated for a heavy-fermion compound, focused ion beam etching enables to introduce a meander-shaped geometry in single crystal platelets, in order to strongly enhance the sample resistance and thus make resistance noise measurements possible. First results indicate a connection of the noise properties with the Kondo effect in the investigated material.
Infections with the hepatitis B virus (HBV) or the hepatitis C virus (HCV) lead to complications like the development of cirrhosis or hepatocellular carcinoma. These complications end up in 887,000 and 500,000 deaths per year, respectively. Since the development of new direct acting antiviral agents for HCV in the past years a complete cure of an HCV infection can be achieved in the majority of the patients. In contrast, a complete cure of a chronic HBV infection still remains a challenging problem as current treatment regimens mainly suppress the viral replication and cccDNA as well as integrated DNA still persist in these patients. Several viral and host factors were described to impair the efficacy of treatment regimens or influence the course of the infection. Therefore, in this work viral factors as well as host factors were investigated in HBeAg negative chronic HBV infected patients and in chronic HCV infected patients. In the present study, it was demonstrated that mutations and/or deletions in the HBV basal core promoter (BCP), the precore and the preS domain occur in a genotype-specifc pattern in HBeAg negative HBV infected patients. While the BCP double mutation A1762T/G1764A was found with the highest prevalence in genotype E infected patients, the precore mutation G1896A occurred mostly in genotype B infected patients. Variants in the preS domain could be detected with the highest frequency in patients infected with genotype C. In patients, who had to start an antiviral therapy during the course of the disease, mutations in the precore region could be detected with a higher frequency in the samples right before treatment start in comparison to the baseline sample.
While different HBV genotypes and preS mutations were not associated with HBV-DNA serum levels, precore mutations as well as BCP mutations were significantly associated with HBV-DNA levels. Furthermore, precore mutations showed lower and preS mutations higher HBsAg levels. The HBsAg serum levels varied significantly among the different genotypes. Since HBsAg levels < 1000 IU/ml have been described as a prognostic marker in several studies, the prevalence of patients with HBsAg < 1000 IU/ml was analyzed among the genotypes A - E. While most of the patients infected with HBV genotype B had HBsAg < 1000 IU/ml, only a few patients infected HBV genotype E and A had HBsAg < 1000 IU/ml.
Furthermore, HBV genotype A genomes derived from patients harboring a) A1762T/ G1764A (BCP), b) G1896A/G1899A (precore), c) 15 aa deletion in preS1, d) no mutation (reference genome) were cloned and analyzed in vitro. An enhanced expression but reduced secretion of viral genomes was found in the preS-deletion- and the precore-variant. No differences in the HBsAg production and secretion were observed in the cloned precore- or BCP-variant, while the preS-deletion-variant was characterized with an elevated HBsAg release.
Regarding the secretion of viral and subviral particles, a genotype-specifc pattern of the L/M/SHBs ratio was detected in the serum of patients infected with genotypes A - E. This pattern did not change in the serum of patients, who started antiviral treatment. Secreted HBsAg containing particles displayed a higher density as well as a higher filaments/spheres ratio in genotypes B and D compared to genotypes A, C and E. Population-based and deep sequencing revealed large deletions in the preS domain or preS2 start codon mutations in a certain number of the viral genomes. Theoretically, these mutations/deletions should influence the molecular weight of the expressed protein or abolish the expression of the protein at all. In contrast, LHBs/MHBs were detectable and appeared at the same molecular weight in these patient samples in comparison to patient samples without these mutations. Furthermore, in the in vitro analyses comparing the reference genome and the preS1-deletion genome, it was shown that the deletion indeed influenced the molecular weight of LHBs. Therefore, HBsAg might be expressed from a genetically different source than the released viral genomes, meaning the integrated DNA.
Additionally, in the present study the prevalence of resistance associated substitutions (RASs) in the viral genes NS3, NS5A and NS5B of chronic HCV infected patients was analyzed in correlation to single nucleotide polymorphisms (SNPs) in the interferon-λ4 (IFNL4) gene of the infected patients. No significant correlation was found between IFNL4 SNPs and RASs within NS3/NS5B in the present cohort. In contrast, the frequently detected NS5A RAS Y93H could be significantly associated with beneficial IFNL4 SNPs and a high baseline viral load in HCV genotype 1-infected patients.
Taken together, the present study demonstrated that viral genome mutations as well as the morphology of secreted particles occur in a genotype-dependent pattern in HBeAg negative HBV infected patients with no need of antiviral therapy. As the amount of serum qHBsAg levels varied among the different genotypes, the HBsAg cut-off < 1000 IU/ml should be adapted individually among the various genotypes. Because the composition of the secreted subviral particles varied between the different genotypes, a genotype-specific immune-response might be induced in these patients. Additionally, the results of the present study indicate that in HBeAg negative HBV infected patients with mutations or deletions in the preS domain MHBs and LHBs might be expressed from the integrated DNA and therefore from a genetically different source than the released viral genomes.
Aside from that, the finding of a significant association of the NS5A RAS Y93H with beneficial IFNL4 SNPs in chronic HCV infected patients may explain a lack of a correlation or an inverse correlation of treatment response with the IFNL4 genotype in some NS5A inhibitor-containing IFN-free regimens.
Evoked potentials (EPs) are well established in clinical practice for diagnosis and prognosis in multiple sclerosis (MS). However, their value is limited to the assessment of their respective functional systems. Here, we used transcranial magnetic stimulation (TMS) coupled with electroencephalography (TMS-EEG) to investigate cortical excitability and spatiotemporal dynamics of TMS-evoked neural activity in MS patients. Thirteen patients with early relapsing–remitting MS (RRMS) with a median Expanded Disability Status Scale (EDSS) of 1.0 (range 0–2.5) and 16 age- and gender-matched healthy controls received single-pulse TMS of left and right primary motor cortex (L-M1 and R-M1), respectively. Resting motor threshold for L-M1 and R-M1 was increased in MS patients. Latencies and amplitudes of N45, P70, N100, P180, and N280 TMS-evoked EEG potentials (TEPs) were not different between groups, except a significantly increased amplitude of the N280 TEP in the MS group, both for L-M1 and R-M1 stimulation. Interhemispheric signal propagation (ISP), estimated from the area under the curve of TEPs in the non-stimulated vs. stimulated M1, also did not differ between groups. In summary, findings show that ISP and TEPs were preserved in early-stage RRMS, except for an exaggerated N280 amplitude. Our findings indicate that TMS-EEG is feasible in testing excitability and connectivity in cortical neural networks in MS patients, complementary to conventional EPs. However, relevance and pathophysiological correlates of the enhanced N280 will need further study.
Background: The recurrence rate in lumbar disc herniations (LDH) has been reported between 5 and 25%. There are only few data about this phenomenon that occurs within days of the initial operation. We analyse early recurrent LDH by analysis of data from the German Spine register.
Methods: Data from patients undergoing disc herniation surgery in the lumbar region were extracted from the German Spine Registry between 1st January 2012 and 31st December 2016. Patients with early recurrent LDH within days of initial surgery were separately analysed.
Results: A total of 9310 surgeries for LDH were documented in the German Spine Register. From these patients 115 (1.2%) presented an early recurrent disc surgeries within days of the initial surgery. The mean age was 70 ± 2.50 years. Most affected segment was L4/5 (47 cases, 41%), followed by L3/4 (45 cases, 39%). The most of our patients showed a normal or overweight Body Mass Index. Surgery for early recurrent LDH was associated with a high rate of incidental durotomies (20 cases, 17.6%). In 3 cases (2.6%) therapy with a lumbar drain was necessary.
Conclusions: The rate of early recurrent LDH within days of surgery is 1.2%. Age seems to be an important factor in early recurrent LDH while obesity does not. The data of the German Spine Register seems to have a reliable data collection system that can perform multicentre data analysis. The databases from this Register could be used in the future for various purposes, such as the evaluation of multicentre surgical techniques, results in patients with various surgical procedures and basic research in spine surgery.
Background: Juvenile dermatomyositis (JDM) is the most common inflammatory myopathy in childhood and a major cause of morbidity among children with pediatric rheumatic diseases. The management of JDM is very heterogeneous. The JDM working group of the Society for Pediatric Rheumatology (GKJR) aims to define consensus- and practice-based strategies in order to harmonize diagnosis, treatment and monitoring of JDM.
Methods: The JDM working group was established in 2015 consisting of 23 pediatric rheumatologists, pediatric neurologists and dermatologists with expertise in the management of JDM. Current practice patterns of management in JDM had previously been identified via an online survey among pediatric rheumatologists and neurologists. Using a consensus process consisting of online surveys and a face-to-face consensus conference statements were defined regarding the diagnosis, treatment and monitoring of JDM. During the conference consensus was achieved via nominal group technique. Voting took place using an electronic audience response system, and at least 80% consensus was required for individual statements.
Results: Overall 10 individual statements were developed, finally reaching a consensus of 92 to 100% regarding (1) establishing a diagnosis, (2) case definitions for the application of the strategies (moderate and severe JDM), (3) initial diagnostic testing, (4) monitoring and documentation, (5) treatment targets within the context of a treat-to-target strategy, (6) supportive therapies, (7) explicit definition of a treat-to-target strategy, (8) various glucocorticoid regimens, including intermittent intravenous methylprednisolone pulse and high-dose oral glucocorticoid therapies with tapering, (9) initial glucocorticoid-sparing therapy and (10) management of refractory disease.
Conclusion: Using a consensus process among JDM experts, statements regarding the management of JDM were defined. These statements and the strategies aid in the management of patients with moderate and severe JDM.
The results of this thesis lie in the area of convex algebraic geometry, which is the intersection of real algebraic geometry, convex geometry, and optimization.
We study sums of nonnegative circuit polynomials (SONC) and their related cone, both geometrically and in application to polynomial optimization. SONC polynomials are certain sparse polynomials having a special structure in terms of their Newton polytopes and supports, and serve as a certificate of nonnegativity for real polynomials, which is independent of sums of squares.
The first part of this thesis is dedicated to the convex geometric study of the SONC cone. As main results we show that the SONC cone is full-dimensional in the cone of nonnegative polynomials, we exactly determine the number of zeros of a nonnegative circuit polynomial, and we give a complete and explicit characterization of the number of zeros of SONC polynomials and forms. Moreover, we provide a first approach to the study of the exposed faces of the SONC cone and their dimensions.
In the second part of the thesis we use SONC polynomials to tackle constrained polynomial optimization problems (CPOPs).
As a first step, we derive a lower bound for the optimal value of CPOP based on SONC polynomials by using a single convex optimization program, which is a geometric program (GP) under certain assumptions. GPs are a special type of convex optimization problems and can be solved in polynomial time. We test the new method experimentally and provide examples comparing our new SONC/GP approach with Lasserre's relaxation, a common approach for tackling CPOPs, which approximates nonnegative polynomials via sums of squares and semidefinite programming (SDP). The new approach comes with the benefit that in practice GPs can be solved significantly faster than SDPs. Furthermore, increasing the degree of a given problem has almost no effect on the runtime of the new program, which is in sharp contrast to SDPs.
As a second step, we establish a hierarchy of efficiently computable lower bounds converging to the optimal value of CPOP based on SONC polynomials. For a given degree each bound is computable by a relative entropy program. This program is also a convex optimization program, which is more general than a geometric program, but still efficiently solvable via interior point methods.
Testicular germ cell cancer in a metastatic state is curable with a cisplatin‑based first line chemotherapy. However, 10‑15% of these patients are resistant to first line chemotherapy and are thus left with only palliative options. Immunotherapies and inhibition of angiogenesis used in multiple types of cancer; however, the molecular context of angiogenesis and immune checkpoints in the development and progression of testicular cancers is still unknown. Therefore, the present study performed tissue micro array based analysis of 84 patients with immunohistochemistry of programmed cell death protein 1 (PD‑1), programmed cell death ligand 1 (PD‑L1) and vascular endothelial growth factor receptor 2 (VEGFR2) of testicular cancer and corresponding normal appearing testis tissue, matching the results with clinical data. The results demonstrated that PD‑L1 was significantly upregulated in testicular tumors and that PD‑1 positive cells significantly infiltrated the testicular tumor when compared with normal testicular tissue. VEGFR2 was significantly upregulated in testicular cancer. It was indicated that PD‑1 expressing cytotoxic cells may require pathologic tumor vessels to pass the blood‑testis‑barrier in order to migrate into the tumor. Notably, when matching the clinical data for PD‑1, PD‑L1 and VEGFR2 there were no differences in expression in the different International Germ Cell Cancer Collaborative Group stages of non‑seminoma. These data suggested that the anti‑PD‑1/PD‑L1 immunotherapy and the anti‑angiogenic therapy, sequentially or in combination, may be a promising option in the treatment of testicular cancer.
According to embodied cognition accounts, viewing others’ facial emotion can elicit the respective emotion representation in observers which entails simulations of sensory, motor, and contextual experiences. In line with that, published research found viewing others’ facial emotion to elicit automatic matched facial muscle activation, which was further found to facilitate emotion recognition. Perhaps making congruent facial muscle activity explicit produces an even greater recognition advantage. If there is conflicting sensory information, i.e., incongruent facial muscle activity, this might impede recognition. The effects of actively manipulating facial muscle activity on facial emotion recognition from videos were investigated across three experimental conditions: (a) explicit imitation of viewed facial emotional expressions (stimulus-congruent condition), (b) pen-holding with the lips (stimulus-incongruent condition), and (c) passive viewing (control condition). It was hypothesised that (1) experimental condition (a) and (b) result in greater facial muscle activity than (c), (2) experimental condition (a) increases emotion recognition accuracy from others’ faces compared to (c), (3) experimental condition (b) lowers recognition accuracy for expressions with a salient facial feature in the lower, but not the upper face area, compared to (c). Participants (42 males, 42 females) underwent a facial emotion recognition experiment (ADFES-BIV) while electromyography (EMG) was recorded from five facial muscle sites. The experimental conditions’ order was counter-balanced. Pen-holding caused stimulus-incongruent facial muscle activity for expressions with facial feature saliency in the lower face region, which reduced recognition of lower face region emotions. Explicit imitation caused stimulus-congruent facial muscle activity without modulating recognition. Methodological implications are discussed.
We develop a model that reproduces the average return and volatility spread between sin and non-sin stocks. Our investors do not necessarily boycott sin companies. Rather, they are open to invest in any company while trading off dividends against ethicalness. We show that when dividends and ethicalness are complementary goods and investors are sufficiently risk averse, the model predicts that the dividend share of sin companies exhibits a positive relation with the future return and volatility spreads. Our empirical analysis supports the model's predictions.
Optogenetics offers a unique method to regulate the activity of select neural circuits. However, the electrophysiological consequences of targeted optogenetic manipulation upon the entire circuit remain poorly understood. Analysis of the sensory-CNS-motor circuit in Drosophila larvae expressing eHpHR and ChR2-XXL revealed unexpected patterns of excitability. Optical stimulation of motor neurons targeted to express eNpHR resulted in inhibition followed by excitation of body wall contraction with repetitive stimulation in intact larvae. In situ preparations with direct electrophysiological measures showed an increased responsiveness to excitatory synaptic activity induced by sensory stimulation within a functional neural circuit. To ensure proper function of eNpHR and ChR2-XXL they were expressed in body wall muscle and direct electrophysiological measurements were obtained. Under eNpHR induced hyperpolarization the muscle remained excitable with increased amplitude of excitatory postsynaptic synaptic potentials. Theoretical models to explain the observations are presented. This study aids in increasing the understanding of the varied possible influences with light activated proteins within intact neural circuits.
In the last decade, central bank interventions, flights to safety, and the shift in derivatives clearing resulted in exceptionally high demand for high quality liquid assets, such as German treasuries, in the securities lending market besides the traditional repo market activities. Despite the high demand, the realizable securities lending income has remained economically negligible for most beneficial owners. We provide empirical evidence of pricing inefficiencies in the non-transparent, oligopolistic securities lending market for German treasuries from 2006 to 2015. Consistent with Duffie, Gârleanu and Pedersen (2005)’s theory, we find that the less connected market participants’ interests are underrepresented, evident in the longer maturity segment, where lenders are more likely to be conservative passive investors, such as pension funds and insurance firms. The low price elasticity in this segment hinders these beneficial owners to fully capitalize on the additional income from securities lending, giving rise to important negative welfare implications.
Cervical spine injuries are frequent and often caused by a blunt trauma mechanism. They can have severe consequences, with a high mortality rate and a high rate of neurological lesions.Diagnosis is a three-step process: 1) risk assessment according to the history and clinical features, guided by a clinical decision rule such as the Canadian C-Spine rule; 2) imaging if needed; 3) classification of the injury according to different classification systems in the different regions of the cervical spine.The urgency of treatment is dependent on the presence of a neurological lesion and/or instability. The treatment strategy depends on the morphological criteria as defined by the classification.
In this study we investigate which economic ideas were prevalent in the macroprudential discourse post-crises in order to understand the availability of ideas for reform minded agents. We base our analysis on new findings in the field of ideational shifts and regulatory science, which posit that change-agents engage with new ideas pragmatically and strategically in their effort to have their economic ideas institutionalized. We argue that in these epistemic battles over new regulation, scientific backing by academia is the key resource determining the outcome. We show that the present reforms implemented internationally follow this pattern. In our analysis we contrast the entire discourse on systemic risk and macroprudential regulation with Borio’s initial 2003 proposal for a macroprudential framework. We find that mostly cross-sectional measures targeted towards increasing the resilience of the financial system rather than inter-temporal measures dampening the financial cycle have been implemented. We provide evidence for the lacking support of new macroprudential thinking within academia and argue that this is partially responsible for the lack of anti-cyclical macroprudential regulation. Most worryingly, the financial cycle is largely absent in the academic discourse and is only tacitly assumed instead of fully fledged out in technocratic discourses, pointing to the possibility that no anti-cyclical measures will be forthcoming.
Background: Conversion from calcineurin inhibitor (CNI) therapy to everolimus within 6 months after kidney transplantation improves long-term graft function but can increase the risk of mild biopsy-proven acute cellular rejection (BPAR). We performed a post-hoc analysis of histological data from a randomized trial in order to further analyze histologic information obtained from indication and protocol biopsies up to 5 years after transplantation.
Methods: Biopsy samples obtained up to 5 years post-transplant were analyzed from the randomized ZEUS study, in which kidney transplant patients were randomized at month 4.5 to switch to everolimus (n = 154) or remain on cyclosporine (CsA)-based immunosuppression (n = 146). All patients received mycophenolate and steroids.
Results: At least one investigator-initiated biopsy was undertaken in 53 patients in each group between randomization and year 5, with a mean (SD) of 2.6 (1.7) and 2.2 (1.4) biopsies per patient in the everolimus and CsA groups, respectively. In the everolimus and CsA groups, investigator-initiated biopsies showed (i) BPAR in 12.3 and 7.5% (p = 0.182) of patients, respectively, with episodes graded mild in 22/24 and 18/20 cases (ii) CsA toxicity lesions in 4.5 and 10.3% of patients (p = 0.076) (iii) antibody-mediated rejection in 0.6 and 2.7% of patients (p = 0.204), respectively.
Conclusions: This analysis of histological findings in the ZEUS study to 5 years after kidney transplantation shows no increase in antibody-mediated rejection under everolimus-based therapy with a lower rate of CNI-related toxicity compared to a conventional CsA-based regimen, and confirms the preponderance of mild BPAR seen in the main study after the early switch to CsA-free everolimus therapy.
Trial registration: ClinicalTrials.gov NCT00154310. Date of registration: September 12, 2005.
Background: Subdural hematoma (SDH) is a common disease associated with high morbidity, which is becoming more prominent due to the increasing incidence. Decision for a surgical evacuation is made depending on the clinical appearance and the volume of SDH, wherefore it is important to have a simple ‘bedside’ method to measure and compare the volume of SDH.
Objective: The aim of the study was to verify the accuracy of the simplified ABC/2 volumetric formula to determine a valuable tool for the clinical practice.
Methods: Preoperative CT-scans of 83 patients with SDHs were used for the computer-assisted volumetric measurement via BrainLab® as well as the ABC/2 volumetric measurement. A = largest length (anterior to posterior) of the SDH; B = maximum width (lateral to midline) 90° to A; C = maximum height (coronal plane or multiplication of slices) of the hematoma. These measurements were performed by two independent clinicians in a blinded fashion. Both volumes were compared by linear regression analysis of Pearson and Bland-Altman regression analysis.
Results: Among 100 SDHs, 53% were under an 47% were over 100cm3 showing a well distribution of the hematoma sizes. There was an excellent correlation between computer-assisted volumetric measurement and ABC/2 (R2 = 0.947, p<0.0001) and no undesirable deviation and trend were detected (p = 0.101; p = 0.777). A 95% tolerance region of the ratios of both methods was [0.805–1.201].
Conclusion: The ABC/2 method is a simple and fast bedside formula for the measurement of SDH volume in a timely manner without limited access through simple adaption, which may replace the computer-assisted volumetric measurement in the clinical and research area. Reason for the good accuracy seems to be the spherical form of SDH, which has a similarity to a half ellipsoid.
Descent of testes from a position near the kidneys into the lower abdomen or into the scrotum is an important developmental process that occurs in all placental mammals, with the exception of five afrotherian lineages. Since soft-tissue structures like testes are not preserved in the fossil record and since key parts of the placental mammal phylogeny remain controversial, it has been debated whether testicular descent is the ancestral or derived condition in placental mammals. To resolve this debate, we used genomic data of 71 mammalian species and analyzed the evolution of two key genes (relaxin/insulin-like family peptide receptor 2 [RXFP2] and insulin-like 3 [INSL3]) that induce the development of the gubernaculum, the ligament that is crucial for testicular descent. We show that both RXFP2 and INSL3 are lost or nonfunctional exclusively in four afrotherians (tenrec, cape elephant shrew, cape golden mole, and manatee) that completely lack testicular descent. The presence of remnants of once functional orthologs of both genes in these afrotherian species shows that these gene losses happened after the split from the placental mammal ancestor. These “molecular vestiges” provide strong evidence that testicular descent is the ancestral condition, irrespective of persisting phylogenetic discrepancies. Furthermore, the absence of shared gene-inactivating mutations and our estimates that the loss of RXFP2 happened at different time points strongly suggest that testicular descent was lost independently in Afrotheria. Our results provide a molecular mechanism that explains the loss of testicular descent in afrotherians and, more generally, highlight how molecular vestiges can provide insights into the evolution of soft-tissue characters.
Since its founding in 1993 the International Long-term Ecological Research Network (ILTER) has gone through pronounced development phases. The current network comprises 44 active member LTER networks representing 700 LTER Sites and ~ 80 LTSER Platforms across all continents, active in the fields of ecosystem, critical zone and socio-ecological research. The critical challenges and most important achievements of the initial phase have now become state-of-the-art in networking for excellent science. At the same time increasing integration, accelerating technology, networking of resources and a strong pull for more socially relevant scientific information have been modifying the mission and goals of ILTER. This article provides a critical review of ILTER's mission, goals, development and impacts. Major characteristics, tools, services, partnerships and selected examples of relative strengths relevant for advancing ILTER are presented. We elaborate on the tradeoffs between the needs of the scientific community and stakeholder expectations. The embedding of ILTER in an increasingly collaborative landscape of global environmental observation and ecological research networks and infrastructures is also reflected by developments of pioneering regional and national LTER networks such as SAEON in South Africa, CERN/CEOBEX in China, TERN in Australia or eLTER RI in Europe. The primary role of ILTER is currently seen as a mechanism to investigate ecosystem structure, function, and services in response to a wide range of environmental forcings using long-term, place-based research. We suggest four main fields of activities and advancements for the next decade through development/delivery of a: (1) Global multi-disciplinary community of researchers and research institutes; (2) Strategic global framework and strong partnerships in ecosystem observation and research; (3) Global Research Infrastructure (GRI); and (4) a scientific knowledge factory for societally relevant information on sustainable use of natural resources.
The marine hydrocarbonoclastic bacterium Alcanivorax borkumensis is well known for its ability to successfully degrade various mixtures of n-alkanes occurring in marine oil spills. For effective growth on these compounds, the bacteria possess the unique capability not only to incorporate but also to modify fatty intermediates derived from the alkane degradation pathway. High efficiency of both these processes provides better competitiveness for a single bacteria species among hydrocarbon degraders. To examine the efficiency of A. borkumensis to cope with different sources of fatty acid intermediates, we studied the growth rates and membrane fatty acid patterns of this bacterium cultivated on diesel, biodiesel and rapeseed oil as carbon and energy source. Obtained results revealed significant differences in both parameters depending on growth substrate. Highest growth rates were observed with biodiesel, while growth rates on rapeseed oil and diesel were lower than on the standard reference compound (hexadecane). The most remarkable observation is that cells grown on rapeseed oil, biodiesel, and diesel showed significant amounts of the two polyunsaturated fatty acids linoleic acid and linolenic acid in their membrane. By direct incorporation of these external fatty acids, the bacteria save energy allowing them to degrade those pollutants in a more efficient way. Such fast adaptation may increase resilience of A. borkumensis and allow them to strive and maintain populations in more complex hydrocarbon degrading microbial communities.
The taxanes are effective microtubule-stabilizing chemotherapy drugs that inhibit mitosis, induce apoptosis, and produce regression in a fraction of cancers that arise at many sites including the ovary. Novel therapeutic targets that augment taxane effects are needed to improve clinical chemotherapy response in CCNE1-amplified high grade serous ovarian cancer (HGSOC) cells. In this study, we conducted an siRNA-based kinome screen to identify modulators of mitotic progression in CCNE1-amplified HGSOC cells that may influence clinical paclitaxel response. PLK1 is overexpressed in many types of cancer, which correlates with poor prognosis. Here, we identified a novel synthetic lethal interaction of the clinical PLK1 inhibitor BI6727 and the microtubule-targeting drug paclitaxel in HGSOC cell lines with CCNE1-amplification and elucidated the underlying molecular mechanisms of this synergism. BI6727 synergistically induces apoptosis together with paclitaxel in different cell lines including a patient-derived primary ovarian cancer culture. Moreover, the inhibition of PLK1 reduced the paclitaxel-induced neurotoxicity in a neurite outgrowth assay. Mechanistically, the combinatorial treatment with BI6727/paclitaxel triggers mitotic arrest, which initiates mitochondrial apoptosis by inactivation of anti-apoptotic BCL-2 family proteins, followed by significant loss of the mitochondrial membrane potential and activation of caspase-dependent effector pathways. This conclusion is supported by data showing that BI6727/paclitaxel-co-treatment stabilizes FBW7, a component of SCF-type ubiquitin ligases that bind and regulate key modulators of cell division and growth including MCL-1 and Cyclin E. This identification of a novel synthetic lethality of PLK1 inhibitors and a microtubule-stabilizing drug has important implications for developing PLK1 inhibitor-based combination treatments in CCNE1-amplified HGSOC cells.
The photoregulation of nucleic acids by azobenzene photoswitches has recently attracted considerable interest in the context of emerging biotechnological applications. To understand the mechanism of photoinduced isomerisation and conformational control in these complex biological environments, we employ a Quantum Mechanics/Molecular Mechanics (QM/MM) approach in conjunction with nonadiabatic Surface Hopping (SH) dynamics. Two representative RNA–azobenzene complexes are investigated, both of which contain the azobenzene chromophore covalently attached to an RNA double strand via a β-deoxyribose linker. Due to the pronounced constraints of the local RNA environment, it is found that trans-to-cis isomerization is slowed down to a time scale of ∼10–15 picoseconds, in contrast to 500 femtoseconds in vacuo, with a quantum yield reduced by a factor of two. By contrast, cis-to-trans isomerization remains in a sub-picosecond regime. A volume-conserving isomerization mechanism is found, similarly to the pedal-like mechanism previously identified for azobenzene in solution phase. Strikingly, the chiral RNA environment induces opposite right-handed and left-handed helicities of the ground-state cis-azobenzene chromophore in the two RNA–azobenzene complexes, along with an almost completely chirality conserving photochemical pathway for these helical enantiomers.
Drug-induced liver injury (DILI) has become a major problem for patients and for clinicians, academics and the pharmaceutical industry. To date, existing hepatotoxicity test systems are only poorly predictive and the underlying mechanisms are still unclear. One of the factors known to amplify hepatotoxicity is the tumor necrosis factor alpha (TNFα), especially due to its synergy with commonly used drugs such as diclofenac. However, the exact mechanism of how diclofenac in combination with TNFα induces liver injury remains elusive. Here, we combined time-resolved immunoblotting and live-cell imaging data of HepG2 cells and primary human hepatocytes (PHH) with dynamic pathway modeling using ordinary differential equations (ODEs) to describe the complex structure of TNFα-induced NFκB signal transduction and integrated the perturbations of the pathway caused by diclofenac. The resulting mathematical model was used to systematically identify parameters affected by diclofenac. These analyses showed that more than one regulatory module of TNFα-induced NFκB signal transduction is affected by diclofenac, suggesting that hepatotoxicity is the integrated consequence of multiple changes in hepatocytes and that multiple factors define toxicity thresholds. Applying our mathematical modeling approach to other DILI-causing compounds representing different putative DILI mechanism classes enabled us to quantify their impact on pathway activation, highlighting the potential of the dynamic pathway model as a quantitative tool for the analysis of DILI compounds.
Background: Prolonged immunosuppression or delayed T-cell recovery may favor Epstein-Barr virus (EBV) infection or reactivation after allogeneic hematopoietic stem cell transplantation (HSCT), which can lead to post-transplant lymphoproliferative disease (PTLD) and high-grade malignant B-cell lymphoma. Cytokine-induced killer (CIK) cells with dual specific anti-tumor and virus-specific cellular immunity may be applied in this context.
Methods: CIK cells with EBV-specificity were generated from peripheral blood mononuclear cells (PBMCs), expanded in the presence of interferon-γ, anti-CD3, interleukin (IL)-2 and IL-15 and were pulsed twice with EBV consensus peptide pool. CIK cells with EBV-specificity and conventional CIK cells were phenotypically and functionally analyzed. Additionally, CIK cells with EBV-specificity were applied to a patient with EBV-related PTLD rapidly progressing to highly aggressive B-cell lymphoma on a compassionate use basis after approval and agreement by the regulatory authorities.
Results: Pre-clinical analysis showed that generation of CIK cells with EBV-specificity was feasible. In vitro cytotoxicity analyses showed increased lysis of EBV-positive target cells, enhanced proliferative capacity and increased secretion of cytolytic and proinflammatory cytokines in the presence of EBV peptide-displaying target cells. In addition, 1 week after infusion of CIK cells with EBV-specificity, the patient's highly aggressive B-cell lymphoma persistently disappeared. CIK cells with EBV-specificity remained detectable for up to 32 days after infusion and infusion did not result in acute toxicity.
Discussion: The transfer of both anti-cancer potential and T-cell memory against EBV infection provided by EBV peptide-induced CIK cells might be considered a therapy for EBV-related PTLD.
Im Rahmen dieser Arbeit wurden sRNAs des halophilen Archaeons Haloferax volcanii hinsichtlich ihrer biologischen und ihrer regulatorischen Funktion charakterisiert.
Um einen Überblick über die biologischen Funktionen archaealer sRNAs zu erhalten, wurde eine umfassende phänotypische Charakterisierung von 27 sRNA-Deletionsmutanten im Vergleich zum Wildtyp ausgewertet. Im Zuge dieser phänotypischen Charakterisierungen wurden zehn verschiedene Wachstumsbedingungen, morphologische Unterschiede und Veränderungen in der Zellmotilität untersucht. Hierbei zeigten nahezu alle Deletionsmutanten unter mindestens einer der getesteten Bedingungen phänotypische Unterschiede. Durch den Verlust von sRNAs wurden sowohl sogenannte Gain-of-function als auch Loss-of-function Phänotypen beobachtet. Haloarchaeale sRNAs spielen eine wichtige Rolle beim Wachstum mit verschiedenen Salzkonzentrationen, mit verschiedenen Kohlenstoffquellen und beim Schwärmverhalten, sind jedoch weniger in die Adaptation an diverse Stressbedingungen involviert.
Zur näheren Charakterisierung der regulatorischen Funktion archaealer sRNAs wurden sRNA362, sRNAhtsf468 und sRNA479 mittels molekulargenetischer Methoden wie Northern Blot-Analyse und DNA-Mikroarray sowie bioinformatischer in silico-Analyse untersucht. Das Expressionslevel von sRNA362 konnte bestimmt und potentielle Zielgene für sRNAhtsf468 und sRNA479 identifiziert werden.
Eine vorangegangene Studie zeigte den Einfluss von sRNA30 unter Hitzestress und führte zur Identifikation differentiell produzierter Proteine in Abwesenheit der sRNA. In dieser Arbeit wurde mittels Northern Blot-Analysen die Expression der sRNA30 charakterisiert. Das Wachstum in An- und Abwesenheit von sRNA30 wurde bei 42°C und 51°C phänotypisch charakterisiert und der regulatorische Einfluss der sRNA auf die mRNA differentiell regulierter Proteine durch Northern Blot-Analyse überprüft. Eine Transkriptomanalyse mittels DNA-Mikroarray nach Hitzeschock-Induktion führte zur Identifikation differentiell regulierter Gene involviert in Transportprozesse, Metabolismus, Transkriptionsregulation und die Expression anderer sRNAs. Die differentielle Regulation des Proteoms nach Hitzeschockinduktion in An- und Abwesenheit von sRNA30 konnte bestätigt werden.
Desweiteren wurde in dieser Arbeit sRNA132 und deren phosphatabhängige Regulation der Ziel-mRNA HVO_A0477-80 näher charakterisiert. Eine Induktionskinetik nach Phosphatentzug bestätigte die Bedeutung von sRNA132 für die verstärkte Expression des Operons HVO_A0477-80 unter Phosphatmangel-Bedingungen und verwies auf die Existenz weiterer Regulationsmechanismen. Während vor und nach Phosphatentzug kein Unterschied bezüglich der Zellmorphologie von Wildtyp und Deletionsmutante zu erkennen war, führte das Wachstum mit einem starken Phosphatüberschuss von 5 mM zu einer Zellverlängerung der Deletionsmutante. Die Kompetition der nativen 3‘-UTR des Operons HVO_A0477-80 mit einer Vektor-kodierten artifiziellen 3‘-UTR legt eine Regulation über die Bindung von sRNA132 an die 3‘-UTR nahe. Der Transkriptomvergleich nach Phosphatentzug in An- und Abwesenheit von sRNA132 führte zur Identifikation des Phosphoregulons der sRNA. Zu diesem Phosphoregulon gehören unter anderem zwei Glycerinphosphat-Dehydrogenasen, Transkriptionsregulatoren, eine Polyphosphatkinase und eine Glycerolphosphodiesterase. Zudem waren die Transkriptlevel der beiden ABC-Transporter HVO_A0477-80 und HVO_2375-8 für anorganisches Phosphat und des Transporters HVO_B0292-5 für Glycerinaldehyd-3-Phosphat in Abwesenheit der sRNA verringert. Die beiden ABC-Transportsysteme für anorganisches Phosphat wurden im Rahmen dieser Arbeit deletiert und weiter charakterisiert. Es konnte gezeigt werden, dass das ABC-Transportsystem HVO_2375-8 bei geringen Phosphatkonzentrationen leicht induziert wird und das Transkriptlevel in Anwesenheit von sRNA132 erhöht ist. Wachstumsversuche der jeweiligen Deletionsmutante in direkter Konkurrenz mit dem Wildtyp zeigten, dass keiner der beiden ABC-Transporter den anderen vollständig ersetzen kann und der Wildtyp mit beiden intakten ABC-Transportern unter phosphatlimitierenden Bedingungen einen Wachstumsvorteil besitzt. In silico-Analysen der Promotorbereiche von sRNA und ABC-Transporter legen zudem die Existenz von P-Boxen nahe.
SAFE Newsletter : 2018, Q2
(2018)
Cross-border exchange and comparison of forensic DNA data in the context of the Prüm decision
(2018)
This study, commissioned by the European Parliament’s Policy Department for Citizens’ Rights and Constitutional Affairs at the request of the LIBE Committee, provides an overview of the Prüm regime. It first considers the background of the Prüm Convention and Prüm Decision. The subsequent two chapters summarize the Prüm regime in relation mainly to DNA data looking at value and shortcomings; and ethical, legal and social implications of forensic DNA typing and databasing in relation to the Prüm regime. Finally, based on the analysis, it provides the policy recommendations.
Crystal growth and characterization of cerium- and ytterbium-based quantum critical materials
(2018)
In der Festkörperphysik werden heutzutage Themen wie Supraleitung, Magnetismus und Quantenkritikalität sowohl von experimenteller als auch von theoretischer Seite stark untersucht. Quantenkritikalität und Quantenphasenübergänge können in Systemen erforscht werden, für welche ein Kontroll Parameter existiert, durch den z.B. eine magnetische Ordnung soweit unterdrückt wird, bis der Phasenübergang bei Null Kelvin, bei einem quantenkritischen Punkt (QCP), stattfindet. Vorzugsweise wird quantenkritisches Verhalten an Einkristallen untersucht, da diese in sehr reiner Qualität gezüchtet werden können und da deren gemessenen physikalischen Eigenschaften ausschließlich intrinsisch sind und nicht durch Verunreinigungseffekte überlagert werden. Der Schwerpunkt dieser Arbeit lag auf der Züchtung von Einkristallen und der Charakterisierung von Materialien, die quantenkritische Phänomene aufweisen. Als Ausgangsstoffe dienten dabei Elemente höchstmöglicher Reinheit. Es wurden die Serie YbNi4(P1-xAsx)2 mit einem ferromagnetischen QCP bei x=0,1, die Verbindung YbRh2Si2 mit einem feldinduzierten QCP bei Bcrit = 60mT und die Serie Ce(Ru1-xFex)PO mit einem QCP bei x = 0,86 untersucht. Für alle Verbindungen wurde das Züchtungsverfahren entwickelt, dann wurden Einkristalle gezüchtet und charakterisiert. Die Züchtung wurde zum einen mittels der Bridgman-Methode, zum anderen mit der Czochralski Methode durchgeführt. Neben struktureller und chemischer Charakterisierung der Einkristalle mittels Röntgen-Pulverdiffraktometrie, Laue-Methode und Energie-dispersiver Röntgen-Spektroskopie, wurden auch deren spezifische Wärme, elektrischer Widerstand und Magnetisierung im Temperaturbereich 1,8 – 300 K untersucht. Im weiteren Verlauf wurden die Kristalle in verschiedenen Kooperationen untersucht und bis in den Tieftemperatur- Bereich (20 mK), bei YbRh2Si2 bis in den Submillikelvin-Bereich, charakterisiert. Ausserdem wurden im Rahmen dieser Dissertation Einkristalle weiterer antiferromagnetischer Verbindungen SmRh2Si2, GdRh2Si2, GdIr2Si2, HoRh2Si2 und HoIr2Si2 gezüchtet. Bei diesen Verbindungen stand die Untersuchung elektronischer Oberflächenzustände mittels winkelaufgelöster Photoemissionsspektroskopie im Vordergrund.
Die Forschungsarbeit leistet einen kriminologischen Beitrag zur Systematisierung des Phänomens der sekundären Viktimisierung bei Opfern sexualisierter Gewalt und zeigt gleichzeitig Präventionsansätze auf, die sekundäre Viktimisierung verhindern sollen.
„Sekundäre Viktimisierung“ als die sogenannte „zweite Opferwerdung“ durch soziale Fehlreaktionen einzelner Personen oder gesellschaftlicher Gruppen sowie die Prävention dieses Phänomens ist im Detail noch wenig erforscht. Der Fokus des Forschungs- und Erkenntnisinteresses richtet sich auf die Zielgruppe der Opfer sexualisierter Gewalt, die in ihrer Kindheit sexuell missbraucht und als Erwachsene sekundär viktimisiert wurden. Es wird angenommen, dass Sexualstraftaten, die von den Opfern im Kindesalter erlitten werden, in besonderem Maße die persönliche Unversehrtheit verletzen und dass somit eine zusätzliche sekundäre Viktimisierung als besonders belastend empfunden wird.
Zunächst wird im theoretischen Teil auf wesentliche Begriffe wie sexualisierte Gewalt in Verbindung mit primärer und sekundärer Viktimisierung eingegangen und nimmt deren kriminologische Einordnung vor, stellt das Ausmaß sowie die Spezifika des Phänomens in den Fokus. Dabei wird zunächst der Opferbegriff ausführlich diskutiert, wobei der Opferperspektive viel Raum gegeben wird. Ein weiterer Schwerpunkt liegt auf der Darstellung des aktuellen Forschungsstandes zur sekundären Viktimisierung, insbesondere mit Bezug zu sexualisierter Gewalt.
Im Zentrum des qualitativen Forschungsansatzes stehen folgende Fragen: „Welche Strukturen prägen die Situationen sekundärer Viktimisierung?“ und „Wie ist Prävention von sekundärer Viktimisierung möglich?“. Auf der Grundlage der Forschungsergebnisse wurde ein Präventionskonzept mit praxisorientierten Empfehlungen entwickelt. Zunächst sind typische Strukturen sekundärer Viktimisierung analysiert und in einem Modell verdeutlicht worden. Es ist zu unterscheiden zwischen Strukturen, die sekundäre Viktimisierung begünstigen (Risikofaktoren) sowie Strukturen, die sekundärer Viktimisierung vorbeugen (Schutzfaktoren). Anhand der identifizierten Schutzfaktoren entstand das Modell zur Prävention sekundärer Viktimisierung, aus denen konkrete Präventionsansätze abzuleiten sind.
Hervorgehoben wird die kriminologische Orientierung der Arbeit; wenngleich die Kriminologie interdisziplinär einzuordnen ist, dominiert bei der Analyse die kriminalsoziologische Verortung und speziell die viktimologische Ausrichtung.
Die Tagung rief dazu auf, die Verbindlichkeit von Versprechen als allgemeines Phänomen zu untersuchen, also zu ergründen, inwiefern man unabhängig von ihrer Ausgestaltung in konkreten Rechtsordnungen oder anderen Normensystemen von einer "vor-rechtlichen" Verbindlichkeit sprechen kann. Literarische Texte aller Zeiten bis hin zu den Mythen bezeugen die Bindung an das Wort als Urerfahrung, die von jeder gesellschaftlichen Konvention unabhängig erscheint. Ebenso kennen sie aber Verrat und offenen oder verdeckten Wortbruch, deren Folgen sie thematisieren. Strukturelle Verwandtschaften einerseits und gegenseitige Beeinflussung andererseits der literarischen und der rechtlichen Auseinandersetzung mit dem Versprechen sollten untersucht werden.
This paper examines whether gender features (masculine, feminine, neuter) in German have to be interpreted semantically, along their specific gender, or whether they allow for a gender unrelated interpretation. As to this, two experiments with two different classes of nouns (gender marked and sex marked nouns vs. gender marked and sex neutral nouns) were conducted. The first experiment supports the view that in their function as nominal predicates masculine nouns, contrary to feminine (and neuter) nouns, have the widest extension – which confirms the existence of a ‘Generic Masculine’ (Generisches Maskulinum). On the other hand, the second experiment shows that in their function as subjects masculine nouns, contrary to feminine (and neuter) nouns, are the least flexible agreement controllers – hardly allowing for gender mismatches. Thus, masculine nouns behave differently depending on whether they appear as controllers/sources of agreement or as targets of agreement. The findings are supplemented by corpus data.
"Habt ihr schon mal davon gehört gehabt?" Fällt Ihnen bei diesem Satz etwas auf? Wie würden Sie den Satz interpretieren, insbesondere die Zeitform des Prädikates hören? Weist sie, Ihrer Meinung nach, eher auf Expressivität, seine Abgeschlossenheit, die (Vor-)Vorvergangenheit eines Geschehens oder eine einfache Vergangenheit hin? Im letzteren Fall würde der Satz die gleiche Semantik ausdrücken wie ohne das zweite Partizip II: Habt ihr schon mal davon gehört? Im Fokus dieser Arbeit stehen empirische Evidenzen zum Gebrauch des doppelten Perfekts und Plusquamperfekts in der deutschen Sprache. Im Rahmen dieser Untersuchung wurde ein Fragebogen mit 202 deutschen Muttersprachlern durchgeführt. Die Ergebnisse dieser Studie zeigen, dass das doppelte Plusquamperfekt bei der Interpretation von ca. 86% der untersuchten deutschen Muttersprachler akzeptiert wird. Weiterhin deuten die Ergebnisse dieser Studie auf viele Unterschiede bei der Akzeptanz der doppelten Konstruktionen zwischen Studierenden verschiedener Fachrichtungen hin.
In the paper, German disintegrated verb-final 'obwohl' (‘although’) and 'weil' (‘because’) clauses are compared with constructions in which 'obwohl' and 'weil' precedes clauses with main clause word order. The former constructions constitute independent, yet subsidiary speech acts. Thus, the subordinating connectors and the positioning of the verb do not indicate syntactic but textual dependency. The latter constructions are of a very different kind. Here, 'obwohl' and 'weil' do not form a constituent with the following clause. Instead, they appear as syntactically independent discourse markers connecting two discourse units. As discourse markers, 'obwohl' and 'weil' obtain their special syntactic and semantic properties as elements of the derived, but independent module of Thetic Grammar.
This paper deals with German 'wobei'-clauses and their Italian counterparts. Based on a corpus study of administrative texts, we identify the type and frequency of the Italian constructions that correspond to 'wobei'-clauses. In particular, we will assess to what extent the Italian converb construction gerundio correlates with 'wobei'-clauses. More specifically, we will focus on the thesis put forward by Haspelmath (1995) and Breindl (2014), according to which comitativity is expressed by converb constructions when it applies to state of affairs.
'Je-desto'-Sätze scheinen in struktureller Hinsicht Einzelgänger zu sein. Das Ungewöhnliche ist, dass sie wie eine obligatorische Verb-dritt-Konstruktion daherkommen: An erster Stelle steht scheinbar der durch je eingeleitete Nebensatz im linken Außenfeld bzw. Vor-vor-Feld, dann folgt die desto-Konstituente, die das Vorfeld einnimmt, und dann an dritter Stelle das finite Verb des Matrixsatzes. Angesichts der Semantik der involvierten Konstituenten ist diese Strukturbeschreibung ungewöhnlich und widerspricht plausiblen Erwartungen. Der Aufsatz bietet eine Analyse, nach der der 'je'-Satz und die 'desto'-Konstituente zusammen eine komplexe Konstituente bilden, die eine einzige, ganz reguläre Einheit konstituiert, was bedeutet, dass der Gesamtsatz eine ziemlich reguläre Verb-zweit-Struktur ist.
Im Mittelpunkt Deutsch
(2018)
Background: Electrical stimulation (ES) has a long history of successful use in the clinical treatment of refractory, non-healing bone fractures and has recently been proposed as an adjunct to bone tissue-engineering treatments to optimize their therapeutic potential. This idea emerged from ES’s demonstrated positive effects on stem cell migration, proliferation, differentiation and adherence to scaffolds, all cell behaviors recognized to be advantageous in Bone Tissue Engineering (BTE). In previous in vitro experiments we demonstrated that direct current ES, administered daily, accelerates Mesenchymal Stem Cell (MSC) osteogenic differentiation. In the present study, we sought to define the optimal ES regimen for maximizing this pro-osteogenic effect.
Methods: Rat bone marrow-derived MSC were exposed to 100 mV/mm, 1 hr/day for three, seven, and 14 days, then osteogenic differentiation was assessed at Day 14 of culture by measuring collagen production, calcium deposition, alkaline phosphatase activity and osteogenic marker gene expression.
Results: We found that exposing MSC to ES for three days had minimal effect, while seven and 14 days resulted in increased osteogenic differentiation, as indicated by significant increases in collagen and calcium deposits, and expression of osteogenic marker genes Col1a1, Osteopontin, Osterix and Calmodulin. We also found that cells treated with ES for seven days, maintained this pro-osteogenic activity long (for at least seven days) after discontinuing ES exposure.
Discussion: This study showed that while three days of ES is insufficient to solicit pro-osteogenic effects, seven and 14 days significantly increases osteogenic differentiation. Importantly, we found that cells treated with ES for only seven days, maintained this pro-osteogenic activity long after discontinuing ES exposure. This sustained positive osteogenic effect is likely due to the enhanced expression of RunX2 and Calmodulin we observed. This prolonged positive osteogenic effect, long after discontinuing ES treatment, if incorporated into BTE treatment protocols, could potentially improve outcomes and in doing so help BTE achieve its full therapeutic potential.
Intestinal graft-versus-host disease (GvHD) is a life-threatening, inflammatory donor T cell-mediated complication of allogeneic hematopoietic stem cell transplantation (allo-HSCT). In the light of the reported efficacy of interleukin-23 (IL-23)-blockade to mitigate syngeneic intestinal inflammation in inflammatory bowel disease patients, targeting IL-23 and thereby interleukin-17a (IL-17a) producing T helper (Th17) cells as the T cell subset assumed to be mostly regulated by IL-23, has emerged as a putatively general concept to harness immune-mediated mucosal inflammation irrespective of the underlying trigger. However, the role of Th17 cells during allo-response driven colitis remains ambiguous due to a series of studies with inconclusive results. Interestingly, we recently identified granulocyte-macrophage colony-stimulating factor (GM-CSF+) T cells to be promoted by interleukin-7 (IL-7) signaling and controlled by the activating protein-1 transcription factor family member basic leucine zipper transcription factor ATF-like (BATF) as critical mediators of intestinal GvHD in mice. Given the dual role of BATF, the contribution of IL-23-mediated signaling within donor T cells and bona fide Th17 cells remains to be delineated from the regulation of GM-CSF+ T cells in the absence of BATF. Here, we found in a complete MHC class I-mismatched model that genetic inactivation of the IL-23 receptor (IL-23R) or the transcription factor retinoic acid-related orphan receptor gamma t (RORγt) within donor T cells similarly ablated Th17 cell formation in vivo but preserved the T cells’ ability to induce intestinal GvHD in a compared to wild-type controls indistinguishable manner. Importantly, RORγt-independent manifestation of intestinal GvHD was completely dependent on BATF-regulated GM-CSF+ T cells as BATF/RORγt double-deficient T cells failed to induce colitis and the antibody-mediated blockage of IL-7/IL-7R interaction and GM-CSF significantly diminished signs of intestinal GvHD elicited by RORγt-deficient donor T cells. Finally, in analogy to our murine studies, colonic RORC expression levels inversely correlated with the presence of GvHD in allo-HSCT patients. Together, this study provides a crucial example of a BATF-dependent, however, IL-23R signaling- and RORγt-, i.e., Th17 fate-independent regulation of a colitogenic T cell population critically impacting the current understanding of intestinal GvHD.
We present an open-source Python package to compute information-theoretical quantities for electroencephalographic data. Electroencephalography (EEG) measures the electrical potential generated by the cerebral cortex and the set of spatial patterns projected by the brain's electrical potential on the scalp surface can be clustered into a set of representative maps called EEG microstates. Microstate time series are obtained by competitively fitting the microstate maps back into the EEG data set, i.e., by substituting the EEG data at a given time with the label of the microstate that has the highest similarity with the actual EEG topography. As microstate sequences consist of non-metric random variables, e.g., the letters A–D, we recently introduced information-theoretical measures to quantify these time series. In wakeful resting state EEG recordings, we found new characteristics of microstate sequences such as periodicities related to EEG frequency bands. The algorithms used are here provided as an open-source package and their use is explained in a tutorial style. The package is self-contained and the programming style is procedural, focusing on code intelligibility and easy portability. Using a sample EEG file, we demonstrate how to perform EEG microstate segmentation using the modified K-means approach, and how to compute and visualize the recently introduced information-theoretical tests and quantities. The time-lagged mutual information function is derived as a discrete symbolic alternative to the autocorrelation function for metric time series and confidence intervals are computed from Markov chain surrogate data. The software package provides an open-source extension to the existing implementations of the microstate transform and is specifically designed to analyze resting state EEG recordings.
This study aims at characterizing the diversity and temporal changes of species richness and composition of fungi in an ecotone of a forest border and a meadow in the Taunus mountain range in Germany. All macroscopically visible, epigeous fungi and vascular plants were sampled monthly over three years, together with climatic variables like humidity and temperature that influence fungal diversity and composition as shown by previous studies. In this mosaic landscape, a total of 855 fungal species were collected and identified based on morphological features, the majority of which belonged to Ascomycota (51 %) and Basidiomycota (45 %). Records of fungal species and plant species (218) for this area yielded a fungus to plant species ratio of 4:1, with a plant species accumulation curve that reached saturation. The three years of monitoring, however, were not sufficient to reveal the total fungal species richness and estimation factors showed that a fungus to plant species ratio of 6:1 may be reached by further sampling efforts. The effect of climatic conditions on fungal species richness differed depending on the taxonomic and ecological group, with temporal patterns of occurrence of Basidiomycota and mycorrhizal fungi being strongly associated with temperature and humidity, whereas the other fungal groups were only weakly related to abiotic conditions. In conclusion, long-term, monthly surveys over several years yield a higher diversity of macroscopically visible fungi than standard samplings of fungi in autumn. The association of environmental variables with the occurrence of specific fungal guilds may help to improve estimators of fungal richness in temperate regions.
Die vorliegende Dissertation beschäftigt sich mit der moderierenden Rolle der Elaboriertheit des sportbezogenen Selbstaspekts auf die Verarbeitung selbstrelevanter Informationen im Sport.
Im ersten Kapitel werden aus einer übergeordneten Perspektive heraus zunächst die beiden im Mittelpunkt der Dissertation stehenden Konstrukte Selbst und Identität in einen historischen Kontext gesetzt und begrifflich umrissen. Im Anschluss werden verschiedene Modelle des Selbst vorgestellt. Dabei wird aufgezeigt, dass insbesondere in der sportpsychologischen Forschung bislang eher Inhalte und weniger Strukturen und Prozesse des Selbstkonzepts im Mittelpunkt standen. In der vorliegenden Dissertation wird das Selbst bzw. die Identität als komplexes, dynamisches System aufgefasst, das sowohl die Informationsverarbeitung beeinflusst als auch durch Prozesse der Informationsverarbeitung beeinflusst wird. Im Anschluss stehen Theorien der Selbstwerterhöhung und der Selbstkonsistenz im Mittelpunkt, deren Vertreter unterschiedliche Vorhersagen für die Verarbeitung konsistenter und von der eigenen Selbsteinschätzung positiv abweichender Rückmeldungen postulieren: Während Selbstwerterhöhungstheorien eine Präferenz für positives Feedback vorhersagen, bevorzugen Personen laut Selbstkonsistenztheorien solches Feedback, das mit ihrer eigenen Selbsteinschätzung übereinstimmt. Anschließend werden mit der Art der Reaktion (affektiv vs. kognitiv) und der Elaboriertheit des betroffenen Selbstaspekts zwei Variablen vorgestellt, die moderieren, ob die Informationsverarbeitung eher konsistenztheoretischen (kognitive Reaktion, hohe Elaboriertheit) oder selbstwerterhöhenden (affektive Reaktion, geringe Elaboriertheit) Vorhersagen folgt.
Ausführlicher werden dann mit dem Exercise Self-Schema und der Exercise Identity zwei sportbezogene Konstrukte vorgestellt, die zur Operationalisierung der Elaboriertheit des entsprechenden Selbstaspekts genutzt werden können. Hierbei wird sowohl auf die Messung als auch auf den empirischen Forschungsstand eingegangen und es wird dargestellt, dass die beiden Konstrukte zwar unterschiedlichen theoretischen Denklinien entstammen, auf operationaler Ebene aber weitgehend austauschbar sind.
Das zweite Kapitel enthält einen Überblick über die drei durchgeführten quantitativen empirischen Studien. Studie 1 (N = 530) beschreibt die Übersetzung und Validierung der Exercise Identity Scale ins Deutsche. Dabei wird neben den beiden in der Literatur diskutierten Ein- und Zwei-Faktor-Modellen auch ein Bifaktor-Modell als mögliche Alternative geprüft. Zusätzlich wird die Invarianz der Skala über die Zeit (Abstand: 14 Tage) mit einer Teilstichprobe, die Invarianz zwischen Männern und Frauen mit der Gesamtstichprobe sowie die konvergente Validität über Korrelationen mit verwandten Konstrukten getestet.
Die Studien 2 und 3 widmen sich der eigentlichen Forschungsfrage nach der moderierenden Wirkung der Elaboriertheit auf die Verarbeitung von sportbezogenem selbstrelevantem Feedback. In Studie 2 (Onlinestudie) wird die Elaboriertheit über das Exercise Self-Schema operationalisiert (N = 472). In dieser Studie zeigt sich, dass Personen – unabhängig davon, ob sie ein Selbstschema im Bereich sportlichen Trainings aufweisen oder nicht – Feedback, das von ihrer eigenen Selbsteinschätzung positiv abweicht, gegenüber mit ihrer Selbsteinschätzung übereinstimmendem (konsistentem) Feedback vorziehen. In Studie 3 (Laborstudie, N = 215) werden einige Limitationen der Onlinestudie adressiert, indem u. a. das fingierte Feedback nach einem objektiveren (physiologischen) Test gegeben und die Elaboriertheit mithilfe der kontinuierlichen Exercise Identity Scale gemessen wird. Auch hier zeigt sich die vermutete moderierende Wirkung der Exercise Identity nicht: Bei der affektiven Reaktion dominiert das Selbstwerterhöhungsmotiv; bei der kognitiven zeigt sich zwar ein kleiner Effekt, der allerdings erwartungswidrig ausfällt (Personen mit geringerer Exercise Identity bevorzugten konsistentes gegenüber positivem Feedback). In beiden Studien zeigt sich darüber hinaus ein moderierender Effekt der Elaboriertheit des sportbezogenen Selbstaspekts hinsichtlich des zur Kontrolle mit in das Versuchsdesign einbezogenen negativen Feedbacks.
Im dritten Kapitel wird eine Gesamtdiskussion der Ergebnisse aus einer übergeordneten Perspektive vorgenommen. Die Befunde werden in den bisherigen empirischen Forschungsstand eingeordnet und es werden Grenzen der durchgeführten Studien diskutiert. Implikationen für zukünftige Forschung werden u. a. im Hinblick auf eine Verbindung zwischen der grundlagenorientierten kognitiv-motivationalen Perspektive der vorliegenden Arbeit und einer eher anwendungsorientierten Perspektive im Sinne der Förderung einer Bindung an sportliche Aktivität diskutiert.
This paper gives an account of the unmaking of Soviet workers at the Vernissage in Armenia. I argue that the unmaking of Soviet workers, first, is the irrelevance of Soviet workers as workers once they lost their jobs after the collapse of the Soviet Union and came to the Vernissage to trade. During the Soviet period, private trade was forbidden, and the Soviet government persecuted people who dared to engage in it. Consequently, many people grew up thinking of trade as a criminal activity that was non-productive and parasitic, as opposed to productive work that facilitated the modernization of the USSR. After the dissolution of the USSR, when trade was liberalized and many former Soviet workers were pushed into trade as they lost their jobs, it still retained its quality of not being “real” work, to borrow Roberman’s (2013) wording. Even 25 years after the dissolution of the USSR, former Soviet workers at the Vernissage still want to be identified with their former Soviet occupations and not with trade. However, now engaged in trade, former Soviet workers came up with a “new” way of establishing identity and hierarchy—through production. I describe this “new” way as “the identification game”; employing it, I demonstrate how former Soviet workers at the Vernissage identify and represent themselves as masters, whose work is productive and intellectual. In doing so, they single out resellers, people who resell the work of other masters, by implying that their work is parasitic and selfish. However, this “identification game” is reified only by the older generation of traders, former Soviet workers. The younger generation of traders at the Vernissage, which does not have any experience of being Soviet workers, is disengaged from it, thus undermining the Soviet view of trade as not “real” work and making it irrelevant in the postsocialist era. Thus, I contend that the unmaking of Soviet workers consists in, first, their irrelevance as workers in a postsocialist period, and second, the irrelevance of their ideas about trade as not “real” work. Furthermore, to support my depiction of a master who engages in “the identification game” and a younger-generation trader who is disengaged from it, I give two ethnographic portraits of traders at the Vernissage. I assert that the disengagement of a younger generation of traders at the Vernissage signals a change in the perception of trade as “real” work and runs parallel to the unmaking of Soviet workers.
Die Wandreliefs aus dem Nordwest-Palast Aššurnasirpals II. (883-859 v. Chr.) in Nimrud zählen zu den forschungsgeschichtlich frühesten und bedeutendsten Funden des Alten Orients. Sie befinden sich heutzutage in zahlreichen Sammlungen weltweit und bieten durch ihre Darstellungen einen tiefgreifenden Einblick in die assyrische Kultur. Insbesondere Kontext und Position der Reliefs bieten Hinweise zur Bedeutung der dort angebrachten Figuren. Zwar ist eine ‚Schutzfunktion‘ vergleichbarer Repräsentationen textlich bezeugt – jedoch bisher nur unter Vorbehalt auf die Reliefdarstellungen zu übertragen. An dieser Stelle kann die Systematisierung ikonographischer Details in Abhängigkeit von ihrem Anbringungsort konzeptionelle Aspekte erkennbar machen.
Durch eine relationale Datenbank und dreidimensionale Visualisierungstechniken wird geprüft, ob die stilistische Variationsbreite ikonographischer Details eine potentielle Systematik aufweist; ebenso, bis zu welchem Grad die jeweilige Form eines bestimmten Zeichnungsdetails einem intentionalen Anbringungskonzept entspricht. Als Teil dieser Vorgehensweise fungiert die in diesem Zusammenhang generierte 3D-Rekonstruktion als methodisch unterstützende Maßnahme. Sie ermöglicht sowohl eine moderne Zusammenführung ehemals benachbarter Reliefplatten unabhängig ihres gegenwärtigen Aufbewahrungsortes als auch die Wiederherstellung heute kaum noch sichtbarer Gewandverzierungen und Pigmentreste.
Anhand der Ergebnisse wird deutlich, dass eine Systematisierung der Reliefdetails mittels 3D-Modell einen erweiterten Erkenntnisfortschritt impliziert und – nicht zuletzt aufgrund der zurückliegenden Zerstörungen der Palastruine und der damit verbundenen unwiederbringlichen Verluste – auch weitere Untersuchungen unterstützen können.
Continuous blood glucose monitoring reveals enormous circadian variations in pregnant diabetic rats
(2018)
Aim: Diabetes in pregnancy is a major burden with acute and long-term consequences. Its treatment requires adequate diagnosis and monitoring of therapy. Many experimental research on diabetes during pregnancy has been performed in rats. Recently, continuous blood glucose monitoring of non-pregnant diabetic rats revealed an increased circadian variability of blood glucose that made a single blood glucose measurement per day inappropriate to reflect glycemic status. Continuous blood glucose measurement has never been performed in pregnant rats. We wanted to perform continuous blood glucose monitoring in pregnant rats to decipher the influence of pregnancy on blood glucose in diabetic and normoglycemic status.
Methods: We used the transgenic Tet29 diabetes rat model with an inducible knock down of the insulin receptor via RNA interference upon application of doxycycline (DOX) leading to insulin resistant type II diabetes. All Tet29 rats received a HD-XG telemetry implant (Data Sciences International, USA) that measured blood glucose and activity continuously. Rats were divided into four groups and blood glucose was monitored until end of pregnancy or the corresponding period: Tet29 + DOX (diabetic) non-pregnant, Tet29 + DOX (diabetic) pregnant, Tet29 (normoglycemic) non-pregnant, Tet29 (normoglycemic) pregnant.
Results: All analyzed rats displayed a circadian variation in blood glucose concentration. Circadian variability was much more pronounced in pregnant diabetic rats than in normoglycemic pregnant rats. Pregnancy ameliorated variation in blood glucose in diabetic situation. Pregnancy continuously decreased blood glucose during normoglycemic pregnancy. Diabetic rats were less active than normoglycemic rats. We performed a calculation showing that application of continuous blood glucose measurement reduces animal numbers needed to detect a given effect in experimental setting by decreasing variability and SD.
Interpretation: Continuous blood glucose monitoring via a telemetry device in pregnant rats provides a more informative picture of the glycemic situation in comparison to single measurements. This could improve diagnosis and therapy of diabetes, decrease animal numbers within experimental settings, and add another physiological parameter (activity) to the analysis that could be helpful in testing therapeutic concepts targeting blood glucose levels and peripheral muscle function. We propose continuous glucose monitoring as a new tool for the evaluation of pregnant diabetic rats.
Spontaneous brain activity is characterized in part by a balanced asynchronous chaotic state. Cortical recordings show that excitatory (E) and inhibitory (I) drivings in the E-I balanced state are substantially larger than the overall input. We show that such a state arises naturally in fully adapting networks which are deterministic, autonomously active and not subject to stochastic external or internal drivings. Temporary imbalances between excitatory and inhibitory inputs lead to large but short-lived activity bursts that stabilize irregular dynamics. We simulate autonomous networks of rate-encoding neurons for which all synaptic weights are plastic and subject to a Hebbian plasticity rule, the flux rule, that can be derived from the stationarity principle of statistical learning. Moreover, the average firing rate is regulated individually via a standard homeostatic adaption of the bias of each neuron’s input-output non-linear function. Additionally, networks with and without short-term plasticity are considered. E-I balance may arise only when the mean excitatory and inhibitory weights are themselves balanced, modulo the overall activity level. We show that synaptic weight balance, which has been considered hitherto as given, naturally arises in autonomous neural networks when the here considered self-limiting Hebbian synaptic plasticity rule is continuously active.