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Das Projekt »Digi_Gap – Digitale Lücken in der Lehrkräftebildung schließen« wird von 2020 bis 2023 vom Bundesministerium für Bildung und Forschung im Rahmen der Qualitätsoffensive Lehrerbildung (QLB) gefördert (Fördersumme: 1 678 023 Euro) und umfasst fünf Teilprojekte mit 19 WissenschaftlerInnen aus neun Fachbereichen an der Goethe-Universität. Geleitet wird das Projekt von Prof. Dr. Holger Horz (wissenschaftliche Gesamtprojektleitung) und Dr. Claudia Burger (operative Leitung). An der Goethe-Universität ebenfalls durch die QLB gefördert wird »The Next Level«, das Nachfolgeprojekt von »Level« (»Lehrerbildung vernetzt entwickeln)«, mit dem Digi_Gap inhaltlich und strukturell eng verbunden ist. Das Leitungs- und Koordinationsteam (Leitung: Holger Horz & Claudia Burger; Koordination: Johannes Appel und Annika Kreft) von Digi_Gap hat sich den Fragen des UniReport auch zum aktuellen Thema »Homeschooling« gestellt.
Rethinking superdeterminism
(2020)
Quantum mechanics has irked physicists ever since its conception more than 100 years ago. While some of the misgivings, such as it being unintuitive, are merely aesthetic, quantum mechanics has one serious shortcoming: it lacks a physical description of the measurement process. This “measurement problem” indicates that quantum mechanics is at least an incomplete theory—good as far as it goes, but missing a piece—or, more radically, is in need of complete overhaul. Here we describe an approach which may provide this sought-for completion or replacement: Superdeterminism. A superdeterministic theory is one which violates the assumption of Statistical Independence (that distributions of hidden variables are independent of measurement settings). Intuition suggests that Statistical Independence is an essential ingredient of any theory of science (never mind physics), and for this reason Superdeterminism is typically discarded swiftly in any discussion of quantum foundations. The purpose of this paper is to explain why the existing objections to Superdeterminism are based on experience with classical physics and linear systems, but that this experience misleads us. Superdeterminism is a promising approach not only to solve the measurement problem, but also to understand the apparent non-locality of quantum physics. Most importantly, we will discuss how it may be possible to test this hypothesis in an (almost) model independent way.
SUMOylation is a reversible posttranslational modification pathway catalyzing the conjugation of small ubiquitin-related modifier (SUMO) proteins to lysine residues of distinct target proteins. SUMOylation modifies a wide variety of cellular regulators thereby affecting a multitude of key processes in a highly dynamic manner. The SUMOylation pathway displays a hallmark in cellular stress-adaption, such as heat or redox stress. It has been proposed that enhanced cellular SUMOylation protects the brain during ischemia, however, little is known about the specific regulation of the SUMO system and the potential target proteins during cardiac ischemia and reperfusion injury (I/R). By applying left anterior descending (LAD) coronary artery ligation and reperfusion in mice, we detect dynamic changes in the overall cellular SUMOylation pattern correlating with decreased SUMO deconjugase activity during I/R injury. Further, unbiased system-wide quantitative SUMO-proteomics identified a sub-group of SUMO targets exhibiting significant alterations in response to cardiac I/R. Notably, transcription factors that control hypoxia- and angiogenesis-related gene expression programs, exhibit altered SUMOylation during ischemic stress adaptation. Moreover, several components of the ubiquitin proteasome system undergo dynamic changes in SUMO conjugation during cardiac I/R suggesting an involvement of SUMO signaling in protein quality control and proteostasis in the ischemic heart. Altogether, our study reveals regulated candidate SUMO target proteins in the mouse heart, which might be important in coping with hypoxic/proteotoxic stress during cardiac I/R injury.
Hou, Alicia ; Bahr, André ; Raddatz, Jacek ; Voigt, Silke ; Greule, Markus ; Albuquerque, Ana Luiza ; Chiessi, Cristiano Mazur ; Friedrich-Rust, Mireen
Precipitation extremes with devastating socioeconomic consequences within the South American Monsoon System (SAMS) are expected to become more frequent in the near future. The complexity in SAMS behavior, however, poses severe challenges for reliable future projections. Thus, robust paleomonsoon records are needed to constrain the high spatiotemporal variability in the response of SAMS rainfall to different climatic drivers. This study uses Ti/Ca ratios from X‐ray fluorescence scanning of a sediment core retrieved off eastern Brazilian to trace precipitation changes over the past 322 Kyr. The results indicate that despite the spatiotemporal complexity of the SAMS, insolation forcing is the primary pacemaker of variations in the monsoonal system. Additional modulation by atmospheric pCO2 suggests that SAMS intensity over eastern Brazil will be suppressed by rising CO2 emissions in the future. Lastly, our record reveals an unprecedented strong and persistent wet period during Marine Isotope Stage 6 driven by anomalously strong trade winds.
Transcriptional basis for differential thermosensitivity of seedlings of various tomato genotypes
(2020)
Transcriptional reprograming after the exposure of plants to elevated temperatures is a hallmark of stress response which is required for the manifestation of thermotolerance. Central transcription factors regulate the stress survival and recovery mechanisms and many of the core responses controlled by these factors are well described. In turn, pathways and specific genes contributing to variations in the thermotolerance capacity even among closely related plant genotypes are not well defined. A seedling-based assay was developed to directly compare the growth and transcriptome response to heat stress in four tomato genotypes with contrasting thermotolerance. The conserved and the genotype-specific alterations of mRNA abundance in response to heat stress were monitored after exposure to three different temperatures. The transcripts of the majority of genes behave similarly in all genotypes, including the majority of heat stress transcription factors and heat shock proteins, but also genes involved in photosynthesis and mitochondrial ATP production. In turn, genes involved in hormone and RNA-based regulation, such as auxin- and ethylene-related genes, or transcription factors like HsfA6b, show a differential regulation that associates with the thermotolerance pattern. Our results provide an inventory of genes likely involved in core and genotype-dependent heat stress response mechanisms with putative role in thermotolerance in tomato seedlings.
Objective: Although meaning making and specifically autobiographical reasoning are expected to relate to well‐being, findings tend to be mixed. Attempts at meaning making do not always lead to meaning made. We aimed to disentangle these complex relationships and also explore the role of level of education.
Method: Ninety participants (mean age 36.73 years, SD = 7.27; 74.4% women, 25.6% men) who had experienced the loss of a parent through death, going missing, or Alzheimer's disease narrated this loss, a sad, a turning point, and a self‐defining memory, and completed questionnaires assessing depression, trauma symptoms, and protracted grief. Three aspects of autobiographical reasoning (quantity, valence, and change‐relatedness of self‐event connections) were related to meaning made (sophistication of meaning making) and symptom level.
Results: Years of education correlated both with positive implications of autobiographical reasoning and with meaning made. The quantity, positivity, and change‐relatedness of attempts at meaning making (self‐event connections) predicted accomplished meaning made, and positivity alone predicted less prolonged grief.
Conclusions: Adapting the life story after a loss such that change of the self is acknowledged and positive change can be constructed helps finding meaning and lowering protracted grief. These changes in narrative identity are supported by more years of education.
The interleukin (IL)-1 family has been described for its numerous involvement in the regulation of inflammatory processes. Certain members are able to induce inflammation, whereas others have the capacity to inhibit inflammation. The newly discovered IL-1 family member IL-38 shows interesting and innovative properties. While most of these cytokines are pro-inflammatory mediators, IL-38 appears to enter the smaller circle of anti-inflammatory mediators. As a pattern, IL-38 appears to suppress IL-17-driven chronic or auto-inflammation by working as receptor antagonist. These properties, as well as its beneficial effects in models of inflammatory and autoimmune diseases suggest the possibility of IL-38-based therapies. Nevertheless, its role in the resolution of acute inflammation, thereby preventing chronic inflammation, remains unclear.
The first part of my thesis elucidated the role of IL-38 in the resolution of inflammation. I found that the complete absence of IL-38 in IL-38 KO mice leads to a delayed resolution of inflammation in the zymosan-induced peritonitis mouse model, compared to WT mice. This was marked by a persistent neutrophilia and a lower production of pro-resolving mediators during the resolution phase, such as TGFβ1 production from macrophages following efferocytosis of apoptotic cells. Reduced TGFβ1 production from macrophages coincided with reduced levels of regulatory T cells (Tregs), which are known to promote the resolution of inflammation. Unexpectedly, the TGFβ1 production capacity of macrophages did not influence the induction of Tregs from naïve T cells. Rather, IL-38 KO mice had an accumulation of Tregs in the thymus compared to WT mice. This was caused by an impairment of CD62L expression at the surface of Tregs, which is required for Tregs migration outside of the thymus. Higher Treg numbers in the thymus correlated with lower level of Tregs in peripheral lymphoid organs. Importantly, CD62L expression at the surface of IL-38 KO Tregs in the thymus was restored by injecting IL-38 i.p. for 24h. These data indicate a potential key function of IL-38 in the regulation of Treg migration, which is triggered in many cases of autoimmunity.
The second part of my thesis was to study the role of IL-38 in experimental autoimmune encephalomyelitis (EAE) development, given that EAE is IL-17-dependent. Unexpectedly, IL-38-deficient mice showed strongly reduced clinical scores and histological markers of EAE. This came with reduced inflammatory cell infiltrates, as well as reduced expression of inflammatory markers in the spinal cord. IL-38 mRNA was detected in the spinal cord, mainly by resident and infiltrated phagocytes, but also by other cells, such as ependymal cells. IL-38 was upregulated upon pro-inflammatory stimulation of bone marrow-derived macrophages, and its presence was necessary for a complete activation of inflammatory macrophages. My data suggest an alternative cell-intrinsic role of IL-38 in macrophages to promote inflammation in the central nervous system.
In the last part of my thesis, I initiated a project on the function of IL-38 in B cell physiology and antibody production, given the fact that IL-38 is expressed by B cells. I generated preliminary data showing that the absence of IL-38 in mice decreased antibody production. Furthermore, I showed that IL-38 is particularly expressed by plasma cells in human tonsils. This project remains open and further studies will be conducted to investigate how IL-38 regulates antibody production, both in physiological and autoimmune settings. Understanding the role of IL-38 in autoantibody production could lead to original and innovative therapy for patients suffering from auto-inflammatory disease.
In summary, the different projects of my thesis provide evidence that the pro-resolving function of IL-38 may be indirectly linked to the retention of Tregs in the thymus. Moreover, a possible intracellular role of IL-38 within macrophages was described showing opposite properties in the regulation of inflammation. This function could be causatively involved in EAE development. However, further studies remain to be done to find the mechanism of action by which IL-38 regulates Tregs egression and how it influences the EAE development. Complete understanding of the IL-38 biology and differentiation between its extra- vs potential intracellular functions could make it a promising therapeutic target for chronic inflammatory or autoimmune diseases.
In fifteen European countries, China, and the US, stocks and business equity as a share of total household assets are represented by an increasing and convex function of income/wealth. A parsimonious model fitted to the data shows why background labor- income risk can explain much of this risk-taking pattern. Uncontrollable labor-income risk stresses middle-income households more because labor income is a larger fraction of their total lifetime resources compared with the rich. In response, middle-income households re-duce (controllable) financial risk. Richer households, having less pressure, can afford more risk-taking. The poor take low risk because they avoid jeopardizing their subsistence consumption.
Hubloher, Josephine Joy ; Zeidler, Sabine ; Lamosa, Pedro ; Santos, Helena ; Averhoff, Beate ; Müller, Volker
The stress protectant trehalose is synthesized in Acinetobacter baumannii from UPD‐glucose and glucose‐6‐phosphase via the OtsA/OtsB pathway. Previous studies proved that deletion of otsB led to a decreased virulence, the inability to grow at 45°C and a slight reduction of growth at high salinities indicating that trehalose is the cause of these phenotypes. We have questioned this conclusion by producing ∆otsA and ∆otsBA mutants and studying their phenotypes. Only deletion of otsB, but not deletion of otsA or otsBA, led to growth impairments at high salt and high temperature. The intracellular concentrations of trehalose and trehalose‐6‐phosphate were measured by NMR or enzymatic assay. Interestingly, none of the mutants accumulated trehalose any more but the ∆otsB mutant with its defect in trehalose‐6‐phosphate phosphatase activity accumulated trehalose‐6‐phosphate. Moreover, expression of otsA in a ∆otsB background under conditions where trehalose synthesis is not induced led to growth inhibition and the accumulation of trehalose‐6‐phosphate. Our results demonstrate that trehalose‐6‐phosphate affects multiple physiological activities in A. baumannii ATCC 19606.
Banks are not immune from COVID-19. The economic downturn may drive some banks to the point of non-viability (PONV). If so, is the resolution regime in the Euro-area ready to respond? No, for banks may not have the right amount of the right kind of liabilities to make bail-in work. That could lead to a banking crisis. The Euro area can avoid this risk, by arranging now for a recap later. This would plug the gap between what the failing bank has and what it would need to make bail-in work. To do so, banks would pay – possibly via the contributions they make to the Single Resolution Fund – a commitment fee to a European backstop authority for a mandatory, system-wide note issuance facility. This would compel each bank, as it approached or reached the PONV, to issue to the backstop, and the backstop to purchase from the bank, the obligations the failing bank needs in order to make bail-in work. Such obligations would take the form of “senior-most” non-preferred debt, and bail-in would stop with such debt. That would allow the SRB to use the bail-in tool to resolve the failed bank, reopen it and run it under a solvent wind-down strategy. That protects counterparties and customers and ensures the continuity of critical economic functions. It also keeps investors at risk and promotes market discipline. Above all, it preserves financial stability.
Use banks the right way
(2020)
Huhn, Meik ; Herrero San Juan, Martina ; Melcher, Balint ; Dreis, Caroline ; Schmidt, Katrin G. ; Schwiebs, Anja ; Collins, Janet ; Pfeilschifter, Josef ; Vieth, Michael ; Stein, Jürgen ; Radeke, Heinfried H.
The widely varying therapeutic response of patients with inflammatory bowel disease (IBD) continues to raise questions regarding the unclarified heterogeneity of pathological mechanisms promoting disease progression. While biomarkers for the differentiation of Crohn’s disease (CD) versus ulcerative colitis (UC) have been suggested, specific markers for a CD subclassification in ileal CD versus colonic CD are still rare. Since an altered signature of the tryptophan metabolism is associated with chronic inflammatory disease, we sought to characterize potential biomarkers by focusing on the downstream enzymes and metabolites of kynurenine metabolism. Using immunohistochemical stainings, we analyzed and compared the mucosal tryptophan immune metabolism in bioptic samples from patients with active inflammation due to UC or CD versus healthy controls. Localization-specific quantification of immune cell infiltration, tryptophan-metabolizing enzyme expression and mucosal tryptophan downstream metabolite levels was performed. We found generally increased immune cell infiltrates in the tissue of all patients with IBD. However, in patients with CD, significant differences were found between regulatory T cell and neutrophil granulocyte infiltration in the ileum compared with the colon. Furthermore, we observed decreased kynurenine levels as well as strong kynureninase (KYNU) expression specifically in patients with ileal CD. Correspondingly, significantly elevated levels of the kynurenine metabolite 3-hydroxyanthranilic acid were detected in the ileal CD samples. Highlighting the heterogeneity of the different phenotypes of CD, we identified KYNU as a potential mucosal biomarker allowing the localization-specific differentiation of ileal CD versus colonic CD.
Der 3D‐Druck von geometrisch komplexen Nanostrukturen ist auf dem Weg zu ersten Anwendungen. Die Auswahl an geeigneten Materialien ermöglicht metallische, halbleitende, isolierende, supraleitende und exotische magnetische Eigenschaften. Das 3D‐FEBID‐Verfahren schreibt mit dem Elektronenstrahl eines Raster‐Elektronenmikroskops wie mit einem Nanostift. Das Material wird als Gasstrom von Precursor‐Molekülen über eine Hohlnadel zugeführt. Der Elektronenstrahl ermöglicht die hochlokale Fragmentierung dieser Moleküle, die meist metallische Zielatome enthalten. Die lokale Verweildauer des Strahls steuert den Strukturaufbau in der Vertikalen, während seine seitliche Bewegung zu geneigten, freistehenden Strukturen führt. Eine Herausforderung ist die definierte Strahlsteuerung, um ein CAD‐Modell möglichst präzise in ein reales 3D‐Nanoobjekt zu überführen. Für die Zukunft soll eine simulationsgestützte Software zur Steuerung des Elektronenstrahls auch Laien die Anwendung erleichtern. 3D‐FEBID ist bereits heute ein zuverlässiges und in vielerlei Hinsicht einzigartiges Verfahren zur Direktabscheidung funktionaler Nanostrukturen.
High-energy physics experiments aim to deepen our understanding of the fundamental structure of matter and the governing forces. One of the most challenging aspects of the design of new experiments is data management and event selection. The search for increasingly rare and intricate physics events asks for high-statistics measurements and sophisticated event analysis. With progressively complex event signatures, traditional hardware-based trigger systems reach the limits of realizable latency and complexity. The Compressed Baryonic Matter experiment (CBM) employs a novel approach for data readout and event selection to address these challenges. Self-triggered, free-streaming detectors push all data to a central compute cluster, called First-level Event Selector (FLES), for software-based event analysis and selection. While this concept solves many issues present in classical architectures, it also sets new challenges for the design of the detector readout systems and online event selection.
This thesis presents an efficient solution to the data management challenges presented by self-triggered, free-streaming particle detectors. The FLES must receive asynchronously streamed data from a heterogeneous detector setup at rates of up to 1 TB/s. The real-time processing environment implies that all components have to deliver high performance and reliability to record as much valuable data as possible. The thesis introduces a time-based data model to partition the input streams into containers of fixed length in experiment time for efficient data management. These containers provide all necessary metadata to enable generic, detector-subsystem-agnostic data distribution across the entire cluster. An analysis shows that the introduced data overhead is well below 1 % for a wide range of system parameters.
Furthermore, a concept and the implementation of a detector data input interface for the CBM FLES, optimized for resource-efficient data transport, are presented. The central element of the architecture is an FPGA-based PCIe extension card for the FLES entry nodes. The hardware designs developed in the thesis enable interfacing with a diverse set of detector systems. A custom, high-throughput DMA design structures data in a way that enables low-overhead access and efficient software processing. The ability to share the host DMA buffers with other devices, such as an InfiniBand HCA, allows for true zero-copy data distribution between the cluster nodes. The discussed FLES input interface is fully implemented and has already proven its reliability in production operation in various physics experiments.
NATURAL LANGUAGE (NL) IS A PROMISING ALTERNATIVE INTERFACE TO DATABASE MANAGEMENT SYSTEMS (DBMSs) BECAUSE IT ENABLES NON-TECHNICAL USERS TO FORMULATE COMPLEX QUESTIONS. RECENTLY, DEEP LEARNING HAS GAINED TRACTION FOR TRANSLATING NATURAL LANGUAGE TO SQL. HOWEVER, THE CORE PROBLEM WITH EXISTING DEEP LEARNING APPROACHES IS THAT THEY REQUIRE AN ENORMOUS AMOUNT OF MANUALLY CURATED TRAINING DATA IN ORDER TO PROVIDE ACCURATE TRANSLATIONS. WE PRESENT DBPAL THAT USES A NOVEL TRAINING PIPELINE TO LEARN NL2SQL INTERFACES WHICH SYNTHESIZES TRAINING DATA AND, THUS, DOES NOT RELY ON MANUALLY CURATED TRAINING DATA.
Häußler, Katja Susanne ; Keese, Michael ; Weber, Christian Friedrich ; Geisen, Christof ; Miesbach, Wolfgang
Postoperative thrombotic thrombocytopenic purpura (TTP) shows clinical presentation similar to classical TTP, whereas exact pathophysiological contexts remain unexplained. In this study, we investigated intraoperative and postoperative changes in ADAMTS-13 (a disintegrin and metalloprotease with thrombospondin type 1 motifs, member 13), von Willebrand factor (VWF), large VWF multimers, and interleukin-6 (IL-6) in vascular surgery patients. The objective was to compare the impact of endovascular, peripheral, and aortic surgery on target parameters which are supposed to play a role in surgery-associated TTP. A total of 93 vascular surgery patients were included and divided into 4 groups according to the specific type of intervention they underwent. Blood samples were taken preoperatively, intraoperatively, and postoperatively on days 2 and 4. The ADAMTS-13 activity decreased significantly in 3 of the 4 groups during surgery (from median 81% to 49%, P < .001, in the group undergoing aortoiliacal interventions), whereas the percentage of large VWF multimers increased in all groups of patients. von Willebrand factor antigen increased significantly in all groups on postoperative day 2 and IL-6 increased significantly in the intraoperative and early postoperative period. There was no significant correlation between the intraoperative decrease in ADAMTS-13 and the increase in VWF or IL-6. No patient in this study showed clinical picture of TTP; the precise cause and clinical significance of moderately reduced ADAMTS-13 activity in the perioperative setting have not yet been definitely determined.
Hübner, Hanna ; Kurbacher, Christian M. ; Kuesters, Geoffrey ; Hartkopf, Andreas D. ; Lux, Michael P. ; Huober, Jens ; Volz, Bernhard ; Ţăran, Florin-Andrei ; Overkamp, Friedrich ; Tesch, Hans ; Häberle, Lothar ; Lüftner, Diana ; Wallwiener, Markus ; Müller, Volkmar ; Beckmann, Matthias Wilhelm ; Belleville, Erik ; Rübner, Matthias ; Untch, Michael ; Fasching, Peter Andreas ; Janni, Wolfgang ; Fehm, Tanja ; Kolberg, Hans-Christian ; Wallwiener, Diethelm ; Brucker, Sara Y. ; Schneeweiss, Andreas ; Ettl, Johannes
Background: Eligibility criteria are a critical part of clinical trials, as they define the patient population under investigation. Besides certain patient characteristics, clinical trials often include biomarker testing for eligibility. However, patient-identification mostly relies on the trial site itself and is often a time-consuming procedure, which could result in missing out on potentially eligible patients. Pre-selection of those patients using a registry could facilitate the process of eligibility testing and increase the number of identified patients. One aim with the PRAEGNANT registry (NCT02338167) is to identify patients for therapies based on clinical and molecular data. Here, we report eligibility testing for the SHERBOC trial using the German PRAEGNANT registry.
Methods:Heregulin (HRG) has been reported to identify patients with better responses to therapy with the anti-HER3 monoclonal antibody seribantumab (MM-121). The SHERBOC trial investigated adding seribantumab (MM-121) to standard therapy in patients with advanced HER2-negative, hormone receptor–positive (HR-positive) breast cancer and HRG overexpression. The PRAEGNANT registry was used for identification and tumor testing, helping to link potential HRG positive patients to the trial. Patients enrolled in PRAEGNANT have invasive and metastatic or locally advanced, inoperable breast cancer. Patients eligible for SHERBOC were identified by using the registry. Study aims were to describe the HRG positivity rate, screening procedures, and patient characteristics associated with inclusion and exclusion criteria.
Results: Among 2769 unselected advanced breast cancer patients, 650 were HER2-negative, HR-positive and currently receiving first- or second-line treatment, thus potentially eligible for SHERBOC at the end of current treatment; 125 patients also met further clinical eligibility criteria (e.g. menopausal status, ECOG). In the first/second treatment lines, patients selected for SHERBOC based on further eligibility criteria had a more favorable prognosis than those not selected. HRG status was tested in 38 patients, 14 of whom (36.8%) proved to be HRG-positive.
Conclusion: Using a real-world breast cancer registry allowed identification of potentially eligible patients for SHERBOC focusing on patients with HER3 overexpressing, HR-positive, HER2-negative metastatic breast cancer. This approach may provide insights into differences between patients eligible or non-eligible for clinical trials.
Trial registration: Clinicaltrials, NCT02338167, Registered 14 January 2015 - retrospectively registered.
2019 hat Frankfurt einen Rekord geknackt: Am 25. Juli wurde im Stadtteil Westend die Tageshöchsttemperatur von 40,2 Grad Celsius erreicht. Damit war Frankfurt der heißeste Ort Hessens seit Beginn der Wetteraufzeichnungen im Jahr 1881. Ein Superlativ, der zeigt: Der Klimawandel stellt auch die Städte vor große Herausforderungen. Gesucht werden Wege, um mit seinen Folgen zurechtzukommen.
Schätzungen zufolge sind weltweit etwa 71 Millionen Menschen chronisch mit dem Hepatitis-C-Virus (HCV) infiziert. Im Jahre 2016 sind rund 400.000 Menschen an einer HCV-bedingten Lebererkrankung gestorben, insbesondere aufgrund der Entwicklung von Leberzirrhose und Lebertumoren. Trotz der großen Unterschiede in den Prävalenzschätzungen und der Qualität der epidemiologischen Daten zeigt die jüngste weltweite Bewertung, dass die virämische Ausbreitung der HCV-Infektion (Prävalenz der HCV-RNA) in den meisten Industrieländern, einschließlich der USA, weniger als 1,0% beträgt (www .cdc.gov / Hepatitis / HCV). In einigen osteuropäischen Ländern wie Lettland (2,2%) oder Russland (3,3%) und bestimmten Ländern in Afrika, Ägypten (6,3%) und Gabun (7,0%) oder im Nahen Osten Syriens (3,0%) ist die Prävalenz bemerkenswert höher. In den USA und den am weitesten entwickelten Ländern gilt die gemeinsame Nutzung von Werkzeugezur Herstellung von Arzneimitteln und zur Injektion von Medikamenten (Nadeln) als die häufigste derzeitige Übertragungsart. Die vorherrschende Übertragungsart in Ländern, in denen die Ausbreitung von HCV-Infektionen im Vergleich zu den Industrieländern höher ist, beruht jedoch auf schlechten Methoden zur Infektionskontrolle und unsicherer Handhabung von Injektionsnadeln.
Wenn die chronische Infektion unbehandelt bleibt, kann sich im fortschreitenden Verlauf eine Zirrhose oder ein hepatozelluläres Karzinom bilden (Alter H. J. und Seef L. B. 2000). Die Doppeltherapie, bei der es sich um eine Kombination aus pegyliertem Interferon-α (PEG IFNα) und Ribavirin (riba) handelt, war in einigen Ländern der Dritten Welt bis vor kurzem der goldene Standard für die Behandlung von Patienten mit chronischer Hepatitis C und hat eine anhaltende virologische Reaktion erzielt. Mit nur 50% der mit HCV-Genotyp 1 infizierten Patienten (der häufigere) im Vergleich zu 80% mit Genotyp 2 oder 3, obwohl sie kostspielig und langwierig sind (z. B. 24-48 Wochen) und zahlreiche harte Nebenwirkungen aufweisen, die schwer zu bekämpfen sind tolerieren (Erklärung der National Institutes of Health Consensus Development Conference: Management von Hepatitis C: 2002 - 10.-12. Juni 2002 2002). Die Identifizierung des JFH1 (japanische fulminante Hepatitis Typ 1) -Isolats wurde in einigen in vitro-Studien zu HCV als wichtiger Durchbruch bei der HCV-Behandlung angesehen. Die Verwendung dieses Isolats führte nachfolgend zu einem besseren Verständnis des HCV-Lebenszyklus und der 3D-Strukturen der viralen Proteine. Basierend auf dieser Erkenntnis konnten die ersten direkt wirkenden antiviralen Mittel (DAAs) entwickelt werden, die spezifisch virale Proteine beeinflussen. Die beiden Proteasehemmer (PI) Telaprevir und Boceprevir hemmen die virale NS3-4A-Protease und wurden 2011 als Kombinationstherapie mit PEG IFNα und Ribavirin zugelassen, was die anhaltende virologische Reaktion auf 67-75% erhöhte (Pawlotsky et al. 2015).
Die Optimierung der gegenwärtigen Arzneimittelregime, die Einschränkung des Problems der Mutationsresistenz, die Gestaltung einer individualisierten Therapie, der Zugang zu diesen therapeutischen antiviralen Arzneimitteln und ihr hoher Preis bleiben weiterhin eine Herausforderung (Pawlotsky 2016; Pawlotsky et al. 2015; Sarrazin 2016). Die Entwicklung eines Impfstoffs wird jedoch als größte Herausforderung für die weltweite Kontrolle von HCV angesehen (Bukh 2016). Aus diesem Grund ist es wichtig, weiterhin mehr über den HCV-Lebenszyklus und die Faktoren zu erfahren, die sich auf die Replikation und den gesamten Lebenszyklus auswirken können, um effiziente, qualitativ hochwertige und vor allem leicht zugängliche Behandlungen für alle Menschen weltweit zu entwickeln.
Der Lipidstoffwechsel und insbesondere das Cholesteringleichgewicht werden durch die HCV-Infektion beeinflusst. Die Korrelation zwischen Lipidstoffwechsel und HCV wurde klinisch seit langem beobachtet. In den Leberbiopsien von mit HCV infizierten Patienten wurde ein Anstieg der in den Lipidtröpfchen im Cytosol akkumulierten neutralen Lipide festgestellt (Dienes et al. 1982). Das Hepatitis-C-Virus wurde auch von Hypobetalipoproteinämie, Hypocholesterinämie und Lebersteatose begleitet (Schaefer und Chung 2013). Die Leber ist der primäre Ort für die Synthese, Speicherung und Oxidation von Lipiden und anderen Makromolekülen. Daher ist der Fettstoffwechsel in der Leber für die Aufrechterhaltung der systemischen Nährstoffhomöostase von wesentlicher Bedeutung. Eine Dysregulation des Leberlipidstoffwechsels ist ein Kennzeichen mehrerer Krankheiten wie Diabetes, alkoholische und nichtalkoholische Fettlebererkrankungen sowie parasitäre und virale Infektionen, einschließlich einer HCV-Infektion. (Erklärung der National Institutes of Health Consensus Development Conference: Management von Hepatitis C: 2002 - 10.-12. Juni 2002 2002; Fon Tacer und Rozman 2011; Chen et al. 2013; Reddy und Rao 2006; Visser et al. 2013; Wu und Parhofer 2014)
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Imorde, Laura ; Möltner, Andreas ; Runschke, Maren ; Weberschock, Tobias Bernd ; Rüttermann, Stefan ; Gerhardt-Szép, Susanne
Background: The purpose of this pilot study was to create a valid and reliable set of assessment questions for examining Evidence-based Dentistry (EbD) knowledge. For this reason, we adapted and validated for dental students the Berlin Questionnaire (BQ), which assesses Evidence-based Medicine (EbM) abilities.
Methods: The Berlin Questionnaire was validated with medical residents. We adapted it for use in a dentistry setting. An expert panel reviewed the adapted BQ for content validity. A cross-sectional cohort representing four training levels (EbD-novice dental students, EbD-trained dental students, dentists, and EbM−/EbD-expert faculty) completed the questionnaire. A total of 140 participants comprised the validation set. Internal reliability, item difficulty and item discrimination were assessed. Construct validity was assessed by comparing the mean total scores of students to faculty and comparing proportions of students and faculty who passed each item.
Results: Among the 133 participants (52 EbD-novice dental students, 53 EbD-trained dental students, 12 dentists, and 16 EbM-/ EbD-expert faculty), a statistically significant (p < 0.001) difference was evident in the total score corresponding to the training level. The total score reliability and psychometric properties of items modified for discipline-specific content were acceptable. Cronbach’s alpha was 0.648.
Conclusion: The adapted Berlin Questionnaire is a reliable and valid instrument to assess competence in Evidence-based Dentistry in dental students. Future research will focus on refining the instrument further.
Ingelfinger, Rebecca ; Henke, Marina ; Roser, Luise ; Ulshöfer, Thomas ; Calchera, Anjuli ; Singh, Garima ; Parnham, Michael J. ; Geisslinger, Gerd ; Fürst, Robert ; Schmitt, Imke ; Schiffmann, Susanne
Lichen-forming fungi are symbiotic organisms that synthesize unique natural products with potential for new drug leads. Here, we explored the pharmacological activity of six lichen extracts (Evernia prunastri, Pseudevernia furfuracea, Umbilicaria pustulata, Umbilicaria crustulosa, Flavoparmelia caperata, Platismatia glauca) in the context of cancer and inflammation using a comprehensive set of 11 functional and biochemical in vitro screening assays. We assayed intracellular Ca2+ levels and cell migration. For cancer, we measured tumor cell proliferation, cell cycle distribution and apoptosis, as well as the angiogenesis-associated proliferation of endothelial cells (ECs). Targeting inflammation, we assayed leukocyte adhesion onto ECs, EC adhesion molecule expression, as well as nitric oxide production and prostaglandin (PG)E2 synthesis in leukocytes. Remarkably, none of the lichen extracts showed any detrimental influence on the viability of ECs. We showed for the first time that extracts of F. caperata induce Ca2+ signaling. Furthermore, extracts from E. prunastri, P. furfuracea, F. caperata, and P. glauca reduced cell migration. Interestingly, F. caperata extracts strongly decreased tumor cell survival. The proliferation of ECs was significantly reduced by E. prunastri, P. furfuracea, and F. caperata extracts. The extracts did not inhibit the activity of inflammatory processes in ECs. However, the pro-inflammatory activation of leukocytes was inhibited by extracts from E. prunastri, P. furfuracea, F. caperata, and P. glauca. After revealing the potential biological activities of lichen extracts by an array of screening tests, a correlation analysis was performed to evaluate particular roles of abundant lichen secondary metabolites, such as atranorin, physodic acid, and protocetraric acid as well as usnic acid in various combinations. Overall, some of the lichen extracts tested in this study exhibit significant pharmacological activity in the context of inflammation and/or cancer, indicating that the group lichen-forming fungi includes promising members for further testing.
Inghirami, Gabriele ; Mace, Mark ; Hirono, Yuji ; Del Zanna, Luca ; Kharzeev, Dmitri E. ; Bleicher, Marcus
At the earliest times after a heavy-ion collision, the magnetic field created by the spectator nucleons will generate an extremely strong, albeit rapidly decreasing in time, magnetic field. The impact of this magnetic field may have detectable consequences, and is believed to drive anomalous transport effects like the Chiral Magnetic Effect (CME). We detail an exploratory study on the effects of a dynamical magnetic field on the hydrodynamic medium created in the collisions of two ultrarelativistic heavy-ions, using the framework of numerical ideal MagnetoHydroDynamics (MHD) with the ECHO-QGP code. In this study, we consider a magnetic field captured in a conducting medium, where the conductivity can receive contributions from the electromagnetic conductivity σ and the chiral magnetic conductivity σχ. We first study the elliptic flow of pions, which we show is relatively unchanged by the introduction of a magnetic field. However, by increasing the magnitude of the magnetic field, we find evidence for an enhancement of the elliptic flow in peripheral collisions. This effect is stronger at RHIC than the LHC, and it is evident already at intermediate collision centralities. Next, we explore the impact of the chiral magnetic conductivity on electric charges produced at the edges of the fireball. This initial σχ can be understood as a long-wavelength effective description of chiral fermion production. We then demonstrate that this chiral charge, when transported by the MHD medium, produces a charge dipole perpendicular to the reaction plane which extends a few units in rapidity. Assuming charge conservation at the freeze-out surface, we show that the produced charge imbalance can have measurable effects on some experimental observables, like v1 or ⟨sinϕ⟩. This demonstrates the ability of a MHD fluid to transport the signature of the initial chiral magnetic fields to late times. We also comment on the limitations of the ideal MHD approximation and detail how further development of a dissipative-resistive model can provide a more realistic description of the QGP.
We derive the Bayes estimator of vectors of structural VAR impulse responses under a range of alternative loss functions. We also derive joint credible regions for vectors of impulse responses as the lowest posterior risk region under the same loss functions. We show that conventional impulse response estimators such as the posterior median response function or the posterior mean response function are not in general the Bayes estimator of the impulse response vector obtained by stacking the impulse responses of interest. We show that such pointwise estimators may imply response function shapes that are incompatible with any possible parameterization of the underlying model. Moreover, conventional pointwise quantile error bands are not a valid measure of the estimation uncertainty about the impulse response vector because they ignore the mutual dependence of the responses. In practice, they tend to understate substantially the estimation uncertainty about the impulse response vector.
Aim: Plant life‐forms characterize key morphological strategies that enable large‐scale comparisons of plant communities. This study applies Raunkiær's plant life‐form concept that was developed for temperate climate to a subtropical island flora, in parts, dominated by summer aridity. We quantify how plant life‐form patterns as well as patterns of important plant functional traits (PFTs) relate to important climate and topographic characteristics.
Location: La Palma, Canary Islands.
Taxon: Flora of La Palma.
Methods: We assigned each native plant species a plant life‐form, that is, phanerophyte, chamaephyte, hemicryptophyte, geophyte and therophyte, as well as PFTs (succulence and N‐fixer). We used stacked species distribution models to assess occurrence probability for each species using the Atlantis database (500 m × 500 m grid). We related richness and percentage values for each plant life‐form and PFT to climate and topography.
Results: Plant life‐forms and PFTs showed a clear pattern within geographic but also climate space, while topography had a minor effect. Phanerophytes mainly contributed to the flora in humid areas. Chamaephytes and hemicryptophytes most strongly contributed to the summit scrub flora and, to some degree, also to the arid coastal regions. Geophytes and therophytes were mainly found in dry coastal regions. N‐fixers contributed mainly to warm‐arid and cool‐arid regions, while succulent species were mainly found in arid coastal regions.
Main conclusions: Raunkiær's plant life‐form concept can be comprehensively transferred to a subtropical island flora by adapting to local unfavourable growing conditions, that is, aridity. Using the strong environmental gradients offered by our study island, we identify substantial climate‐driven variation in patterns of plant life‐forms and PFTs that might be used for large‐scale comparisons in macroecological studies. The growth strategies reflected in Raunkiær's plant life‐forms suggest differences in species establishment and coexistence dynamics within different parts of the island's climate space.
Hofstadter-Hubbard physics
(2020)
The Hofstadter model, besides the Haldane and Kane-Mele models, is the most common tight-binding model which hosts topologically nontrivial states of matter. In its time-reversal-symmetric formulation the model can even describe topological insulators. Experimentally, the Hofstadter model was realized with ultracold quantum gases in optical lattices which is a wellcontrolled way to engineer quantum states of tight-binding Hamiltonians. Another established control parameter in ultracold quantum gases are twoparticle, on-site interactions, also known as Hubbard interactions. This work aims at introducing the reader to the concepts of topological states of matter, a collection of corresponding tight-binding models, and the methodology to treat interacting topological states with dynamical mean-field theory.We present recent results for inhomogeneous, interacting systems, spinimbalanced magnetic systems, propose experimental detection methods, and extensions to three-dimensional topological states.
To support future research based on natural sciences collection data, DiSSCo (Distributed System of Scientific Collections) – the European Research Infrastructure for Natural Science Collections – adopts Digital Object Architecture as the basis for its planned data infrastructure. Using the outputs of one Research Data Alliance (RDA) interest group (IG) and five working groups (WGs) we show how RDA recommendations and supporting documents have been applied to the various stages of the DiSSCo data lifecycle.
This paper offers a description and account of the patterns of 'ex-situ' focus in Dagbani. We show that there are two syntactic strategies for creating 'ex-situ' focus in the language, one involving A’-movement to the left periphery, and the second involving base generation in the left periphery combined with coreference to a resumptive pronoun. Furthermore, we argue that subjects are difficult to move from Spec,TP to Spec,CP in the left-periphery because of 'anti-locality', which creates a tension when trying to focus subjects, which are required to derivationally fill the specifier of both positions. We further show that what looks to be a two-way distinction between the behaviour of subjects and non-subjects in the language is in fact a three-way distinction between subjects that are focussed to a local left-periphery, subjects that are focussed to a non-local left-periphery, and non-subjects. These distinctions arise due to there being two methods for Dagbani to resolve the antilocality problem of subject movement, and so local subjects solve the problem differently to non-local subjects.
This Policy White Paper assesses several main elements of ECB’s upcoming review of its monetary policy strategy, announced in January 2020. Four aspects of the review are discussed in detail: i) ECB’s definition of price stability and the arguments for and against inflation targeting; ii) the scope of ECB’s objectives, considering financial stability, employment and the sustainability of the environment; iii) an update of ECB’s economic and monetary analyses to assess the risks to price stability; iv) the ECB’s communication practice. Furthermore, an overview of the ECB’s monetary policy strategy and its last evaluation in 2003 is given.
Diese Masterarbeit fragt nach Anschlussmöglichkeiten der Schriften Bruno Latours an die Postwachstumsdiskussion an der Friedrich-Schiller-Universität Jena. Im ersten Schritt wird die Jenaer Debatte um Degrowth in der Tradition der kritischen Theorie verortet und inhaltlich anhand der Begriffe der »Wachstumskritik« und der »sozial-ökologischen Transformation« rekonstruiert. Zweitens folgt die Rekonstruktion Latours anhand dreier Werkphasen seit Anfang der 90ger Jahre. Im dritten Schritt geht es darum, Latour mit der Jenaer Debatte ins Gespräch zu bringen. Dabei stößt der Autor auf einen sozial-theoretischen Graben zwischen beiden Denkschulen. Das darf allerdings nicht darüber hinwegtäuschen, dass Latours Werke viele praktische Anknüpfungspunkte bereithalten, wie eine sozial-ökologische Transformation im Sinne der Postwachstumsdebatte gelingen kann.
Diese Arbeit beschäftigt sich mit linearen inversen Problemen, wie sie in einer Vielzahl an Anwendungen auftreten. Diese Probleme zeichnen sich dadurch aus, dass sie typischerweise schlecht gestellt sind, was in erster Linie die Stabilität betrifft. Selbst kleinste Messfehler haben enorme Konsequenzen für die Rekonstruktion der zu bestimmenden Größe.
Um eine robuste Rekonstruktion zu ermöglichen, muss das Problem regularisiert, dass heißt durch eine ganze Familie abgeänderter, stabiler Approximationen ersetzt werden. Die konkrete Wahl aus der Familie, die sogenannte Parameterwahlstrategie, stützt sich dann auf zusätzliche ad hoc Annahmen über den Messfehler. Typischerweise ist dies im deterministischen Fall die Kenntnis einer oberen Schranke an die Norm des Datenfehlers, oder im stochastischen Fall, die Kenntnis der Verteilung des Fehlers, beziehungsweise die Einschränkung auf eine bestimmte Klasse von Verteilungen, zumeist Gaußsche. In der vorliegenden Arbeit wird untersucht, wie sich diese Informationen unter der Annahme der Wiederholbarkeit der Messung gewinnen lassen. Die Daten werden dabei aus mehreren Messungen gemittelt, welche einer beliebigen, unbekannten Verteilung folgen, wobei die zur Lösung des Problems unweigerlich notwendige Fehlerschranke geschätzt wird. Auf Mittelwert und Schätzer wird dann ein klassisches Regularisierungsverfahren angewandt. Als Regularisierungen werden größtenteils Filter-basierte Verfahren behandelt, die sich auf die Spektralzerlegung des Problems stützen. Als Parameterwahlstrategien werden sowohl einfache a priori-Wahlen betrachtet, als auch das Diskrepanzprinzip als adaptives Verfahren. Es wird Konvergenz für unbekannte beliebige Fehlerverteilungen mit endlicher Varianz sowie für Weißes Rauschen (bezüglich allgemeiner Diskretisierungen) nachgewiesen. Schließlich wird noch die Konvergenz des Diskrepanzprinzips für ein stochastisches Gradientenverfahren gezeigt, als erste rigorose Analyse einer adaptiven Stoppregel für ein solches nicht Filter-basiertes Regularisierungsverfahren.
Jahn-Kuch, Daniela ; Domke, Andreas ; Bitsche, Sarah Margarethe ; Stöger, Herbert ; Avian, Alexander ; Jeitler, Klaus ; Posch, Nicole ; Siebenhofer-Kroitzsch, Andrea
Background: Austria has recently been embroiled in the complex debate on the legalization of measures to end life prematurely. Empirical data on end-of-life decisions made by Austrian physicians barely exists. This study is the first in Austria aimed at finding out how physicians generally approach and make end-of-life therapy decisions.
Methods: The European end-of-life decisions (EURELD) questionnaire, translated and adapted by Schildmann et al., was used to conduct this cross-sectional postal survey. Questions on palliative care training, legal issues, and use of and satisfaction with palliative care were added. All Austrian specialists in hematology and oncology, a representative sample of doctors specialized in internal medicine, and a sample of general practitioners, were invited to participate in this anonymous postal survey.
Results: Five hundred forty-eight questionnaires (response rate: 10.4%) were evaluated. 88.3% of participants had treated a patient who had died in the previous 12 months. 23% of respondents had an additional qualification in palliative medicine. The cause of death in 53.1% of patients was cancer, and 44.8% died at home. In 86.3% of cases, pain relief and / or symptom relief had been intensified. Further treatment had been withheld by 60.0%, and an existing treatment discontinued by 49.1% of respondents. In 5 cases, the respondents had prescribed, provided or administered a drug which had resulted in death. 51.3% of physicians said they would never carry out physician-assisted suicide (PAS), while 30.3% could imagine doing so under certain conditions. 38.5% of respondents supported the current prohibition of PAS, 23.9% opposed it, and 33.2% were undecided. 52.4% of physicians felt the legal situation with respect to measures to end life prematurely was ambiguous. An additional qualification in palliative medicine had no influence on measures taken, or attitudes towards PAS.
Conclusions: The majority of doctors perform symptom control in terminally ill patients. PAS is frequently requested but rarely carried out. Attending physicians felt the legal situation was ambiguous. Physicians should therefore receive training in current legislation relating to end-of-life choices and medical decisions. The data collected in this survey will help political decision-makers provide the necessary legal framework for end-of-life medical care.
The hydrogen-dependent carbon dioxide reductase is a soluble enzyme complex that directly utilizes hydrogen (H2) for the reduction of carbon dioxide (CO2) to formate in the first step of the acetyl-coenzyme A- or Wood-Ljungdahl pathway (WLP). HDCR consists of 2 catalytic subunits, a hydrogenase and a formate dehydrogenase (FDH) and two small subunits carrying iron-sulfur clusters. The enzyme complex has been purified and characterized from two acetogenic bacteria, from the mesophile Acetobacterium woodii and, recently, from the thermophile Thermoanaerobacter kivui. Physiological studies toward the importance of the HDCR for growth and formate metabolism in acetogens have not been carried out yet, due to the lack of genetic tools. Here, we deleted the genes encoding HDCR in T. kivui taking advantage of the recently developed genetic system. As expected, the deletion mutant (strain TKV_MB013) did not grow with formate as single substrate or under autotrophic conditions with H2 + CO2. Surprisingly, the strain did also not grow on any other substrate (sugars, mannitol or pyruvate), except for when formate was added. Concentrated cell suspensions quickly consumed formate in the presence of glucose only. In conclusion, HDCR provides formate which was essential for growth of the T. kivui mutant. Alternatively, extracellularly added formate served as terminal electron acceptor in addition to CO2, complementing the growth deficiency. The results show a tight coupling of multi-carbon substrate oxidation to the WLP. The metabolism in the mutant can be viewed as a coupled formate + CO2 respiration, which may be an ancient metabolic trait.
Jakobi, Katja ; Beyer, Sandra ; Koch, Alexander ; Thomas, Dominique Jeanette ; Schwalm, Stephanie ; Zeuzem, Stefan ; Pfeilschifter, Josef ; Grammatikos, Georgios
Hepatocellular carcinoma (HCC) shows a remarkable heterogeneity and is recognized as a chemoresistant tumor with dismal prognosis. In previous studies, we observed significant alterations in the serum sphingolipids of patients with HCC. This study aimed to investigate the in vitro effects of sorafenib, which is the most widely used systemic HCC medication, on the sphingolipid pathway as well as the effects of inhibiting the sphingolipid pathway in HCC. Huh7.5 and HepG2 cells were stimulated with sorafenib, and inhibitors of the sphingolipid pathway and cell proliferation, viability, and concentrations of bioactive metabolites were assessed. We observed a significant downregulation of cell proliferation and viability and a simultaneous upregulation of dihydroceramides upon sorafenib stimulation. Interestingly, fumonisin B1 (FB1) and the general sphingosine kinase inhibitor SKI II were able to inhibit cell proliferation more prominently in HepG2 and Huh7.5 cells, whereas there were no consistent effects on the formation of dihydroceramides, thus implying an involvement of distinct metabolic pathways. In conclusion, our study demonstrates a significant downregulation of HCC proliferation upon sorafenib, FB1, and SKI II treatment, whereas it seems they exert antiproliferative effects independently from sphingolipids. Certainly, further data would be required to elucidate the potential of FB1 and SKI II as putative novel therapeutic targets in HCC.
Das Hepatozelluläre Karzinom (HCC) ist die sechsthäufigste Krebsart mit der zweithäufigsten krebsbedingten Letalität. Sorafenib ist bereits seit über 10 Jahren die einzige verfügbare und zugelassene systemische Chemotherapie. Allerdings zeigen Patienten oft eine Resistenz gegenüber Sorafenib.
In zahlreichen Krebsarten konnte bereits gezeigt werden, dass Sphingolipide bei der Tumorentwicklung und Chemoresistenz eine wichtige Rolle spielen. Sphingolipide sind bioaktive Lipidmoleküle, welche unteranderem für die Beeinflussung verschiedener Signalwege intra- und extrazellulär verantwortlich sind. So konnte gezeigt werden, dass das Verhältnis zwischen Sphingosin-1-Phosphat (S1P) und Ceramiden eine wichtige Rolle für das Überleben von Zellen spielt, wobei eine Verschiebung des Verhältnisses zugunsten des S1P meist eine proliferative Wirkung auf Zellen hat. Für die Phosphorylierung des Sphingosins zu S1P sind die zwei Enzyme Sphingosinkinase 1 und 2 (SPHK1/2) verantwortlich.
Es gibt bereits Studien, die nachweisen konnten, dass diese Enzyme gerade in Tumorzellen verstärkt exprimiert werden. Auf der anderen Seite kann eine verstärkte Bildung von Ceramiden die Apoptose der Tumorzellen verstärken. Daher ist es nicht verwunderlich, dass der Sphingolipid-Stoffwechsel einen interessanten Angriffspunkt für die Krebstherapie darstellt. Aus diesem Grund sollte in der vorliegenden Arbeit zunächst untersucht werden, ob Sorafenib einen Einfluss auf den Sphingolipid Stoffwechsel hat. Weiter sollte untersucht werden, ob die Beeinflussung des Sphingolipid-Stoffwechsels die Effekte von Sorafenib potenzieren könnte.
Es konnte zunächst gezeigt werden, dass Sorafenib die mRNA-Expression verschiedener Enzyme, die das Verhältnis zwischen Ceramiden und S1P regulieren, beeinflussen kann. Es wurde weiter untersucht, wie sich der Ceramidsynthase Inhibitor FB1 auf die Proliferation und die Induktion der Apoptose auswirkt. Dies wurde ebenfalls mit SLP (SPHK1 Inhibitor), SLM (SPHK2 Inhibitor) und SKI II, einem unspezifischen Inhibitor beider Sphingosinkinasen, untersucht. Es wurden weiter die Einflüsse aller verwendeten Substanzen auf die Bildung verschiedener Sphingolipide untersucht.
Hierbei konnte gezeigt werden, dass Sorafenib in der Lage ist, die Proliferation der Zellen zu hemmen und die Apoptose-Induktion zu fördern. Weiter führte Sorafenib zu einer Akkumulation der Dihydroceramide. Was wiederrum weder mit SKI II, FB1; SLP noch SLM beobachtet werden konnte. Der signifikante Anstieg der Dihydroceramid-Konzentrationen konnte mit dem durch Sorafenib induzierten oxidativen Stress in Verbindung gebracht werden.
SLP und SLM waren nicht in der Lage, die Effekte von Sorafenib auf die Proliferation zu potenzieren. Die Kombination von Sorafenib mit SLP oder SLM führte jedoch in den Huh7.5 Zellen zu einer drastischen Reduktion des S1P-Spiegel.
FB1 und SKI II führten zu einer stärkeren Hemmung der Proliferation als Sorafenib. Wobei gezeigt werden konnte, dass beide Substanzen die Ceramid-Spiegel tendenziell eher vermindern und die S1P-Spiegel erhöhen. Durch die Stimulation mit FB1 kam es sogar zu einer signifikanten Erhöhung der S1P-Spiegel. Es scheint, dass der Einfluss von FB1 und SKI II auf die Proliferation der Zellen unabhängig vom Sphingolipid-Stoffwechsel ist. Diese scheinen eher über andere Mechanismen zu wirken. Es könnte von Interesse sein, gerade diese Signalwege von SKI II im HCC weiter zu untersuchen, da SKI II bereits in Mausmodellen anderer Krebsarten vielversprechende Ergebnisse zeigte.
Jamali, Arezoo ; Hadjati, Jamshid ; Madjd, Zahra ; Mirzaei, Hamid Reza ; Thalheimer, Frederic Bastian ; Agarwal, Shiwani ; Bönig, Halvard-Björn ; Ullrich, Evelyn ; Hartmann, Jessica
Natural killer (NK) cells are a noteworthy lymphocyte subset in cancer adoptive cell therapy. NK cells initiate innate immune responses against infections and malignancies with natural cytotoxicity, which is independent of foreign antigen recognition. Based on these substantive features, genetically modifying NK cells is among the prime goals in immunotherapy but is currently difficult to achieve. Recently, we reported a fully human CAR19 construct (huCAR19) with remarkable function in gene-modified T-cells. Here, we show efficient and stable gene delivery of huCAR19 to primary human NK cells using lentiviral vectors with transduction efficiencies comparable to those achieved with NK cell lines. These huCAR19 NK cells display specific and potent cytotoxic activity against target cells. To improve homing of NK cells to the bone marrow, we augmented huCAR19 NK cells with the human CXCR4 gene, resulting in transgenically augmented CAR NK cells (TRACKs). Compared to conventional CAR NK cells, TRACKs exhibit enhanced migration capacity in response to recombinant SDF-1 or bone marrow stromal cells while retaining functional and cytolytic activity against target cells. Based on these promising findings, TRACKs may become a novel candidate for immunotherapeutic strategies in clinical applications.
Mit der COLTRIMS-Technik können immer kompliziertere Reaktionen untersucht werden, dabei steigt aber die Zahl der zu detektierenden Reaktionsfragmente. Der Nachweis von Ionen ist üblicherweise gut möglich, da die entsprechenden Flugzeiten groß sind im Vergleich zur Totzeit der benutzten Detektoren. Elektronen hingegen sind sehr leicht und erreichen den Detektor innerhalb von wenigen 10 ns. Aktuelle Detektoren erlauben aber nur den Nachweis weniger Elektronen und es werden somit neue Detektoren benötigt, um alle Teilchen nachzuweisen. Ziel dieser Arbeit war es also, einen Detektor zu entwickeln, der dies erreicht.
Zu Beginn dieser Monografie wird die COLTRIMS-Technik vorgestellt. Die Experimente mit dieser Messmethode finden hauptsächlich mit einer Laufzeitanode statt. Diese stößt aber bei dem Nachweis von mehreren Teilchen an ihre Grenzen und manche Experimente können nur unvollständig analysiert werden.
Damit ein neuer Detektor entwickelt werden kann, muss erst verstanden werden, wie die zu detektierenden Teilchen/Signale entstehen und wie ihre Eigenschaften sind. Aus diesem Grund wird das Sekundärteilchen-erzeugende MCP ausführlich vorgestellt.
Weiterhin gibt diese Arbeit einen umfassenden Überblick über bereits realisierte Anoden. Verschiedene Repräsentanten der fünf Anodenarten (Flächen-, Streifen-/Pixel-, Laufzeit-, Kamera-, sowie Halbleiter-Anode) werden vorgestellt und bewertet.
Mit diesem Wissen konnten drei Ansätze für neue Anoden entwickelt, designt, produziert, getestet und bewertet werden. Alle neu entwickelten Anoden benutzen Leiterplatinen als Basis und werden in derselben Vakuumkammer getestet. Auch wenn die Detektionsprinzipien der drei getesteten Detektoren unterschiedlich sind, so verläuft die Auskopplung, Verarbeitung und Digitalisierung der Signale nach dem gleichen Schema. Außerdem wurden im Rahmen dieser Arbeit diverse Algorithmen entwickelt und programmiert, mit deren Hilfe die Signalauswertung und Positionsbestimmung erfolgt.
Das dritte Kapitel beschreibt die neu entwickelte Draht-Harfen-Anode. Dieser Detektor besteht aus vielen kurzen Drähten die parallel auf Rahmen aus Leiterplatinen gespannt werden. Aus dieser Anode ließ sich im Rahmen dieser Arbeit aber kein funktionsfähiger Detektor entwickeln und es wird empfohlen, diesen Ansatz nicht weiterzuverfolgen.
Im Kapitel über die Pixel-Anode mit Streifenauslese wird ein Ansatz vorgestellt, bei dem die Elektronenwolke von einem Muster aus leitenden Rauten absorbiert wird. Es wurde ein funktionsfähiger Detektor mit MAMA-Verschaltung realisiert. Die aktive Fläche ist mit einem Durchmesser von 50 mm aber zu klein. Eine große Variante der Anode ist in der realisierten Form aber nicht als Detektor geeignet.
Als dritter neuer Detektor wird die Streifen-Laufzeit-Anode beschrieben. Diese besteht aus einem rechteckigen Muster von Pixeln, die in einer Richtung über eine Zeitverzögerung ausgelesen werden. Dieser Ansatz ist sehr vielversprechend und es ließen sich nicht nur einzelne Teilchen nachweisen, sondern auch beim Aufbruch eines D2+-Moleküls konnten beide Fragmente gemessen werden.
Das letzte Kapitel befasst sich mit weiteren Konzepten, die als Detektor realisiert werden könnten.
Determination of the effective dose of bone marrow mononuclear cell therapy for bone healing in vivo
(2020)
Janko, Maren Carina ; Pöllinger, Sabrina ; Schaible, Alexander ; Bellen, Marlene ; Schröder, Katrin ; Heilani, Myriam Widad ; Fremdling, Charlotte ; Marzi, Ingo ; Nau, Christoph Heinrich Eugen ; Henrich, Dirk ; Verboket, René
Introduction: Cell-based therapy by bone marrow mononuclear cells (BMC) in a large-sized bone defect has already shown improved vascularization and new bone formation. First clinical trials are already being conducted. BMC were isolated from bone marrow aspirate and given back to patients in combination with a scaffold within some hours. However, the optimal concentration of BMC has not yet been determined for bone healing. With this study, we want to determine the optimal dosage of the BMC in the bone defect to support bone healing.
Material and methods: Scaffolds with increasing BMC concentrations were inserted into a 5 mm femoral defect, cell concentrations of 2 × 106 BMC/mL, 1 × 107 BMC/mL and 2 × 107 BMC/mL were used. Based on the initial cell number used to colonize the scaffolds, the groups are designated 1 × 106, 5 × 106 and 1 × 107 group. Bone healing was assessed biomechanically, radiologically (µCT), and histologically after 8 weeks healing time.
Results: Improved bone healing parameters were noted in the 1 × 106 and 5 × 106 BMC groups. A significantly higher BMD was observed in the 1 × 106 BMC group compared to the other groups. Histologically, a significantly increased bone growth in the defect area was observed in group 5 × 106 BMC. This finding could be supported radiologically.
Conclusion: It was shown that the effective dose of BMC for bone defect healing ranges from 2 × 106 BMC/mL to 1 × 107 BMC/mL. This concentration range seems to be the therapeutic window for BMC-supported therapy of large bone defects. However, further studies are necessary to clarify the exact BMC-dose dependent mechanisms of bone defect healing and to determine the therapeutically effective range more precisely.
Jansen, Martin ; Engler, Marc ; Blumer, Luka Moritz ; Rumiz, Damián I. ; Aramayo, José Luis ; Krone, Oliver
At a site in the Bolivian Chiquitano region composed by a mosaic of pastureland and primary Chiquitano Dry Forest&nbsp;(CDF) we conducted a camera-trapping study to (1) survey the mammals, and (2) compare individual Jaguar numbers&nbsp;with other Chiquitano sites. Therefore, we installed 13 camera stations (450 ha polygon) over a period of six months.&nbsp;On 1,762 camera-days and in 1,654 independent capture events, we recorded 24 mammalian species that represent the&nbsp;native fauna of large and medium-sized mammals including apex-predators (Puma, Jaguar), meso-carnivores (Ocelot,&nbsp;Jaguarundi, Margay), and large herbivores (Tapir, Collared and White lipped Peccary). We identified six adult Jaguars&nbsp;and found indications of successful reproductive activity. Captures of Jaguars were higher in CDF than in altered habitats.&nbsp;In summary, we believe that (1) the mammal species richness, (2) the high capture numbers of indicator species,&nbsp;and (3) the high capture numbers of Jaguar indicate that our study area has a good conservation status. Future efforts&nbsp;should be undertaken to keep this, and monitoring programs in this region are necessary to further evaluate the potential&nbsp;importance of the Chiquitano region as a possible key region for mammals, especially Jaguars, in South America.
Jaque, Jenny ; Wanke, Eileen M. ; Müller, Ruth ; Bauer, Jan ; Ohlendorf, Daniela Maren ; Mache, Stefanie ; Klingelhöfer, Doris ; Quarcoo, David
URPOSE: Today, the majority of medical graduates in countries such as the UK, the US or Germany are female. This poses a major problem for workforce planning especially in urology. We here use first the first time the previously established Brüggmann Groneberg (BG) index to assess if female academic career options advance in urology.
METHODS: Different operating parameters (student population, urology specialist population, urology chair female:male (f:m) ratio) were collected from the Federal Office of Statistics, the Federal Chamber of Physicians and the medical faculties of 36 German universities. Four time points were monitored (2000, 2005, 2010 and 2015). From these data, female to male (f:m) ratios and the recently established career advancement (BG) index have been calculated.
RESULTS: The German hospital urology specialists' f:m ratios were 0.257 (499 female vs. 1944 male) for 2015, 0.195 for 2010, 0.133 for 2005 and 0.12 for 2000. The career advancement (BG) index was 0.0007 for 2000, 0,0005 for 2005, 0.094 for 2010 and 0.073 for 2015. The decrease from 2010 to 2015 was due to an increase in the f:m ratio of hospital urologists and female medical students.
CONCLUSION: The BG index clearly illustrated that there is an urgent need for special academic career funding programs to counteract gender problems in urology. The BG index has been shown to be an excellent tool to assess female academic career options and will be very helpful to assess and document positive or negative changes in the next decades.
»Wir müssen lernen, magische Kugeln zu gießen, die gleichsam wie Zauberkugeln des Freischützen nur die Krankheitserreger treffen.« Dieser Anspruch von Paul Ehrlich klingt in der aktuellen Corona-Pandemie zutreffender denn je und schien auch die Redner bei der Feierstunde zur Vergabe des Paul Ehrlich- und Ludwig Darmstaedter-Preises 2020 bewegt zu haben.
Von Hierarchien, Tunneln und Grenzen : preisgekrönte Forschung: drei Ausgezeichnete im Porträt
(2020)
Sie gehört zu den Höhepunkten im Programm der Vereinigung von Freunden und Förderern: die Akademische Feier, bei der im festlichen Rahmen die Preise an die Nachwuchswissenschaftlerinnen und -wissenschaftler vergeben werden. Doch in diesem Sommer musste auch diese Veranstaltung wegen der Corona-Pandemie gecancelt werden. Drei der elf Ausgezeichneten werden in diesem UniReport vorgestellt: die Philosophin Prof. Dr. Lisa Herzog, der Physiker Dr. Sebastian Eckart und die Politikwissenschaftlerin Eva-Maria Schäfferle.
Die junge Professorin der Romanistik wirkt einsam in ihrem großen, fast leeren Büro im fünften Stock des IG-Farben-Gebäudes. Nichts geht in Corona-Zeiten für die Linguistin voran – in Forschung und Lehre ist Sol Lago angewiesen auf die unmittelbare Zusammenarbeit mit Probanden und Studierenden. »Ich wäre so froh, wenn wir endlich mit dem neuen Eye-Tracker loslegen könnten«, so die gebürtige Argentinierin, die vor Ideen sprudelt. Drei Sprachwissenschaftler vom Institut für romanische Sprachen, Prof. Dr. Esther Rinke, Prof. Dr. Jacopo Torregrossa und Prof. Dr. Sol Lago, haben jeweils 10 000 Euro in das transportable Gerät investiert. Die noch fehlende Summe von knapp 5 000 Euro hat die Freundesvereinigung beigesteuert.
Apps und »virtuelle Brillen« werden in der Behandlung von Stimmungs- und Angststörungen zunehmend zur Realität. Auch das Team von Prof. Dr. Andreas Reif an der Klinik für Psychiatrie, Psychosomatik und Psychotherapie der Goethe-Universität beteiligt sich an klinischen Studien. »In unserer neuen VR-Angst-Ambulanz werden wir mit bereits in Studien erprobten VR-Modulen arbeiten. So können wir aktuelle Erkenntnisse zügig in der Therapie umsetzen«, so Reif. In einem zweiten Projekt geht es um Behandlung von Depressionen mit Methoden der Virtuellen Realität (VR).
Jawinski, Philippe ; Markett, Sebastian ; Sander, Christian ; Huang, Jue ; Ulke, Christine ; Hegerl, Ulrich ; Hensch, Tilman
Based on Eysenck’s pioneering work, CNS arousal has long been considered an encouraging biological candidate that may explain individual differences in human personality. Yet, results from empirical studies remained inconclusive. Notably, the vast majority of published results have been derived from small samples, and EEG alpha power has usually served as exclusive indicator for CNS arousal. In this study, we selected N = 468 individuals of the LIFE-Adult cohort and investigated the associations between the Big Five personality traits and CNS arousal by using the low-resolution electromagnetic tomography-based analysis tool VIGALL. Our analyses revealed that subjects who reported higher levels of extraversion and openness to experience, respectively, exhibited lower levels of CNS arousal in the resting state. Bayesian and frequentist analysis results were especially convincing for openness to experience. Among the lower-order personality traits, we obtained strongest evidence for neuroticism facet ‘impulsivity’ and reduced CNS arousal. We regard these findings as well in line with the postulations of Eysenck and Zuckerman and consistent with the assumptions of the ‘arousal regulation model’. Our results also agree with meta-analytically derived effect sizes in the field of individual differences research, highlighting the need for large studies with at least several hundreds of subjects.
This thesis discusses important questions of the beam dynamics in the proton-lead operation in the Large Hadron Collider (LHC) at CERN in Geneva. In two time blocks of several weeks in the years 2013 and 2016, proton-lead collisions have so far been successfully generated in the LHC and used by the experiments at the LHC. One reason for doubts regarding the successful operation in proton-lead configuration was the fact that the beams have to be accelerated with different revolution frequencies. There is long-range repulsion between the beams, since both beams share the beam chamber around the interaction points. Because of the different revolution frequencies, the positions of the interaction between the beams shift each revolution. This can lead to resonant excitation and to an increase in the transverse beam emittance, as was observed in the Relativistic Heavy-Ion Collider (RHIC). In this thesis, simulations for the LHC, RHIC and the High-Luminosity Large Hadron Collider (HL-LHC) are performed with a new model. The results for RHIC show relative growth rates of the emittances of the gold beam in gold-deuteron operation in RHIC from 0.1 %/s to 1.5 %/s. Growth rates of this magnitude were observed experimentally in RHIC. Simulations for the LHC show no significant increase of the emittance of the lead beam for different intensities of the counter-rotating beam. The simulation results confirm the measured stability of the beams in the LHC and the issue of strongly increasing emittances in RHIC is reproduced. Also, no significant increase of the emittance is predicted for the Future Circular Collider (FCC) and the HL-LHC.
Using a frequency-map analysis, this work verifies whether the interaction of the lead beam with the much smaller proton beam in the proton-lead operation of the LHC leads to diffusion within the lead beam. Experiences at HERA at DESY in Hamburg and at SppS at CERN have shown that the lifetime of the larger beam can rapidly decrease under certain circumstances. The results of the simulation show no chaotic dynamics near the beam centre of the lead beam. This result is supported by experimental observation.
A program code has been developed which calculates the beam evolution in the LHC by means of coupled differential equations. This study shows that the growth rates of the lead beam due to intra-beam scattering is overestimated and that particle bunches of the lead beam lose more intensity than assumed in the model. The analysis also shows that bunches colliding in a detector suffer additional losses that increase with decreasing crossing angle at the interaction point.
In this work, 2016 data from beam-loss monitors in combination with the luminosity and the loss rate of the beam intensity are used to determine the cross section of proton-lead collisions at the center-of-mass energy of 8.16 TeV. Beam-loss monitors that mainly detect beam losses that are not caused by the collision process itself are used to determine the total cross section via regression. An analysis of the data recorded in 2016 at the center-of-mass energy of 8.16 TeV resulted in a total cross section of σ=(2.32±0.01(stat.)±0.20(sys.)) b. This corresponds approximately to a hadronic cross section of σ(had)=(2.24±0.01(stat.)±0.21(sys.)) b. This value deviates only by 5.7 % from the theoretical value σ(had)=(2.12±0.01) b.
The simulation code for determining the beam evolution is also used to estimate the integrated luminosity of a future one-month run with proton-lead collisions. The result of the study shows that in the future the luminosity in the ATLAS and CMS experiments will increase from 15/nb per day in 2016 to 30/nb per day, which is a significant increase in terms of the performance. This operation, however, requires the use of the TCL collimators to protect the dispersion suppressors at ATLAS and CMS from collision fragments.
This work also gives an outlook on the expected luminosity production in proton-nucleus operation using ion species lighter than lead ions. For example, a change from proton-lead to proton-argon collisions would increase the integrated luminosity from monthly 0.8/nb to 9.4/nb in ATLAS and CMS. This is an increase of one order of magnitude and approximately a doubling of the integrated nucleon-nucleon luminosity. There may be a test operation with proton-oxygen collisions in 2023, which will last only a few days and will be operated with a low luminosity. The LHCf experiment (LHCb experiment) would achieve the desired integrated luminosity of 1.5/nb (2/nb) within 70h (35h) beam time.
Jemaà, Mohamed ; Sime, Wondossen ; Abassi, Yasmin ; Lasorsa, Vito Alessandro ; Køhler, Julie Bonne ; Michaelis, Martin ; Cinatl, Jindrich ; Capasso, Mario ; Massoumi, Ramin
Drug resistance of childhood cancer neuroblastoma is a serious clinical problem. Patients with relapsed disease have a poor prognosis despite intense treatment. In the present study, we aimed to identify chemoresistance gene expression signatures in vincristine resistant neuroblastoma cells. We found that vincristine-resistant neuroblastoma cells formed larger clones and survived under reduced serum conditions as compared with non-resistant parental cells. To identify the possible mechanisms underlying vincristine resistance in neuroblastoma cells, we investigated the expression profiles of genes known to be involved in cancer drug resistance. This specific gene expression patterns could predict the behavior of a tumor in response to chemotherapy and for predicting the prognosis of high-risk neuroblastoma patients. Our signature could help chemoresistant neuroblastoma patients in avoiding useless and harmful chemotherapy cycles.
Die Menschheit sieht sich mit dem drohenden Zerfall ihrer Existenzgrundlage konfrontiert: Die Folgen des menschengemachten Klimawandels sind global zunehmend sichtbar und betreffen immer mehr Regionen (IPCC 2019: o. S.). Diese Auswirkungen zeigen sich auf sozialer wie auf wirtschaftlicher Ebene: Die Kosten der bereits entstandenen Klimaschäden sind für beide genannten Bereiche enorm (Edenhofer et al. 2019: 22). Wissenschaftler*innen sind bei der Suche nach einem Ausweg aus dieser Krisensituation zu dem Schluss gekommen, dass die Reduktion der CO2-Emissionen dringend nötig ist, um den menschengemachten Klimawandel einzudämmen (IPCC 2019: o. S.). Die von Wissenschaftler*innen als am effizientesten bewertete Maßnahme zur Reduktion der ausgestoßenen CO2-Emissionen ist die Bepreisung ebendieser in Form einer CO2-Steuer (Bundesrat 2018: 78; vgl., Gagnebin et al. 2019; Tiezzi 2005: 1598; Williams III et al. 2015: 195). Mittlerweile haben vierzig Länder und über zwanzig Städte eine derartige Maßnahme eingeführt oder entwerfen Konzepte zur Etablierung ebendieser (Farrell 2015: 31). Problematisch ist jedoch, dass die CO2-Abgabe häufig mit einem regressiven Effekt einhergeht und dementsprechend besonders finanziell vulnerable Gruppen überproportional belastet. Am Fallbeispiel der Schweiz untersucht die vorliegende Arbeit, inwiefern sich die CO2-Lenklungsabgabe auf ökonomisch vulnerable Gruppen auswirkt. Das Untersuchungsjahr ist hierbei 2018. Mithilfe der intersektionalen Theorie sowie der Methode des Gender Impact Assessments herausgearbeitet, welche Vulnerabilitätsaspekte neben dem Einkommen einen Anhaltspunkt für eine überproportionale ökonomische Belastung durch die CO2-Lenkungsabgabe darstellen.
Jerkic, Silvija-Pera ; Brinkmann, Folke ; Calder, Alistair ; Casey, Alicia ; Dishop, Megan ; Griese, Matthias ; Kurland, Geoffrey ; Niemitz, Mandy ; Nyilas, Sylvia ; Schramm, Dirk ; Schubert, Ralf ; Tamm, Michael ; Zielen, Stefan ; Rosewich, Martin
Bronchiolitis obliterans (BO) is a rare, chronic form of obstructive lung disease, often initiated with injury of the bronchiolar epithelium followed by an inflammatory response and progressive fibrosis of small airways resulting in nonuniform luminal obliteration or narrowing. The term BO comprises a group of diseases with different underlying etiologies, courses, and characteristics. Among the better recognized inciting stimuli leading to BO are airway pathogens such as adenovirus and mycoplasma, which, in a small percentage of infected children, will result in progressive fixed airflow obstruction, an entity referred to as postinfectious bronchiolitis obliterans (PIBO). The present knowledge on BO in general is reasonably well developed, in part because of the relatively high incidence in patients who have undergone lung transplantation or bone marrow transplant recipients who have had graft-versus-host disease in the posttransplant period. The cellular and molecular pathways involved in PIBO, while assumed to be similar, have not been adequately elucidated. Since 2016, an international consortium of experts with an interest in PIBO assembles on a regular basis in Geisenheim, Germany, to discuss key areas in PIBO which include diagnostic workup, treatment strategies, and research fields.
Jhang, Genie ; Estee, Justin ; Barney, Jonathan ; Cerizza, Giordano ; Kaneko, Masanori ; Lee, Jung Woo ; Lynch, William G. ; Isobe, Tadaaki ; Kurata-Nishimura, Mizuki ; Murakami, Tetsuya ; Tsang, Chun Yuen ; Tsang, Betty ; Wang, Rensheng ; Ahn, Deuk Soon ; Atar, Leyla ; Aumann, Thomas ; Baba, Hidetada ; Boretzky, Konstanze ; Brzychczyk, Janusz ; Chiga, Nobuyuki ; Fukuda, Naoki ; Gašparić, Igor ; Hong, Byungsik ; Horvat, Andrea ; Ieki, Kazuo ; Inabe, Naohito ; Kim, Y.J. ; Kobayashi, Taizo ; Kondo, Yosuke ; Lasko, Pawel ; Lee, H.S. ; Leifels, Yvonne ; Łukasik, Jerzy ; Manfredi, Juan ; McIntosh, Alan B. ; Morfouace, Pierre ; Nakamura, Takashi ; Nakatsuka, N. ; Nishimura, Shunji ; Olsen, Robert ; Otsu, Hideaki ; Pawłowski, Piotr ; Pelczar, Krzysztof ; Rossi, Dominic M. ; Sakurai, Hiroyoshi ; Santamaria, Clementine ; Sato, Hiromi ; Scheit, Heiko ; Shane, Rebecca ; Shimizu, Yohei ; Simon, Haik ; Snoch, Aleksandra ; Sochocka, Anna ; Sosin, Zbigniew ; Sumikama, Toshiyuki ; Suzuki, Hiroshi ; Suzuki, Daisuke ; Takeda, Hiroshi ; Tangwancharoen, Suwat ; Törnqvist, Hans Toshihide ; Togano, Yasuhiro ; Xiao, Zhi-Gang ; Yennello, Sherry J. ; Yurkon, John ; Zhang, Youhong ; Colonna, Maria ; Cozma, Dan ; Danielewicz, Paweł ; Elfner, Hannah ; Ikeno, Natsumi ; Ko, Che Ming ; Mohs, Justin ; Oliinychenko, Dmytro ; Ono, Akira ; Su, Jun ; Jia Wang, Yong ; Wolter, Hermann ; Xu, Jun ; Zhang, Ying-Xun ; Zhang, Zhen
In the past two decades, pions created in the high density regions of heavy ion collisions have been predicted to be sensitive at high densities to the symmetry energy term in the nuclear equation of state, a property that is key to our understanding of neutron stars. In a new experiment designed to study the symmetry energy, the multiplicities of negatively and positively charged pions have been measured with high accuracy for central 132Sn+124Sn, 112Sn+124Sn, and 108Sn+112Sn collisions at E/A = 270 MeV with the SπRIT Time Projection Chamber. While individual pion multiplicities are measured to 4% accuracy, those of the charged pion multiplicity ratios are measured to 2% accuracy. We compare these data to predictions from seven major transport models. The calculations reproduce qualitatively the dependence of the multiplicities and their ratios on the total neutron and proton number in the colliding systems. However, the predictions of the transport models from different codes differ too much to allow extraction of reliable constraints on the symmetry energy from the data. This finding may explain previous contradictory conclusions on symmetry energy constraints obtained from pion data in Au+Au system. These new results call for still better understanding of the differences among transport codes, and new observables that are more sensitive to the density dependence of the symmetry energy.
Three types of post-translation modifications (PTMs) containing N-glycosylation, phosphorylation, ubiquitylation were characterized in diffuse large B-cell lymphoma (DLBCL) on a global scale using quantitative mass spectrometry based proteomics technology in this study.
DLBCL is the most common type of malignant lymphomas and has a heterogeneous gene expression profiling, phenotype and clinical response to chemotherapy. DLBCL is a good model for the correct classification of cancers into molecularly different subtypes, which benefits for the selection of rational therapeutic strategies. It resulted in two histologically indistinguishable subtypes-activated B-cell-like (ABC) subgroup and germinal center B-cell-like (GCB) subgroup according to gene expression profiling. Signals originating from the B-cell receptor (BCR), the key protein on the surface of B cells, promote growth and survival of DLBCL. Antigen-dependent/independent BCR signaling is found in DLBCL subtypes.
Recent researches reveal that glycosylation plays role in human cells via site-specific regulation. Aberrant N-glycosylation in BCR-related effectors, such as, CD79a, immunoglobulin M or G (IgM or IgG), has been found to be associated with lymphoid malignancies. However, accurate quantification of intact glycopeptides and their individual glycan moieties in a cell-wide manner is still challenging. Here we established a site-specific quantitative N-glycoproteomics platform termed SugarQuant. It included a fast sample preparation workflow using Protein Aggregation Capture (PAC), an optimized multi-notch MS3 acquisition workflow (Glyco-SPS-MS3), a self-developed R-based tool (GlycoBinder). The robustness and accuracy of quantitation in SugarQuant were proved in a study using the different amounts of TMT-labelled IgM N-glycopeptides spiked into a background of TMT-labelled yeast peptides. Next, we used SugarQuant to identify and quantify more than 5000 unique glycoforms in Burkitt’s lymphoma cells treated with a series of doses of 2-deoxy-2-fluoro-L-fucose (2FF) and determine the more accurate site-specific glycosylation changes that occurred upon inhibition of fucosylation compared to using MS2 analysis. It revealed that 2FF-sensitive N-glycosylation on key players in BCR-mediated signaling in DG75. Furthermore, 2FF treatment also affects phosphorylation of the key players involving in B cell receptor signaling.
Then we investigated the site-specific quantitative N-glycoproteome in the cell lines of DLBCL subtypes using SugarQuant. More than 7000 unique intact glycopeptides (glycoforms) were quantified in five ABC DLBCL and four GCB DLBCL cell lines. The glycoproteome mapping (intact glycopeptide expressions) in each cell line allows to segregate DLBCL subtypes. The majority of these glycoforms were from the key cell-surface BCR effectors, such as IgM, CD79 and PTPRC. Lastly, we investigated the change of fucosylated glycopeptides in TMD8 cell line upon knockout of the fucosyltransferase FUT8, which is responsible for core-fucose synthesis, and by the treatment with 2FF. The results revealed that FUT8 might also regulate the synthesis of sub/terminal fucose on glycan chain and the inhibition of fucosylation increased the sialyated glycopeptide expression.
Phosphorylation is involved in regulating multiple processes as an important mediator in BCR signaling. Likewise, ubiquitylation plays vital roles in the activation of the nuclear factor-kappaB (NF-κB) pathway in BCR signaling. There are two vital upstream BCR-proximal tyrosine kinases, Bruton’s tyrosine kinase (BTK) and spleen tyrosine kinase (SYK), which regulate the auto-phosphorylation and phosphorylation of other proteins in BCR signaling pathway. Here we investigated the dynamics of downstream phosphorylation and ubiquitylation signaling in ABC DLBCL and GCB DLBCL cell lines upon the inhibitions of BTK and SYK using quantitative proteomics strategy. In the phosphoproteome analysis, a large dataset of quantified phosphorylation sites was obtained in the three ABC and four GCB DLBCL cell lines. BCR signaling in the subtypes of DLBCL cell lines was found to be highly individual in distinct cell lines. These significantly regulated phosphorylation events in each cell line with individual treatment were involved in multiple Reactome pathways, such as, M phase, signaling by Rho GTPases and diseases of signal transduction. Moreover, the gene regulation-related biological processes including chromosome organization and medication, DNA metabolic process, nuclear export, were involved in the DLBCL cell lines. In the ubiquitinome analysis, we identified more than 15,000 ubiquitylation sites in two ABC and one GCB cell lines upon the inhibition of BTK and SYK. The different ubiquitylation events observed in ABC and GCB subtypes revealed distinct BCR signaling pathways in two subtypes. The similar signaling perturbations across each cell line upon BTK and SYK inhibition, which were obtained from the significantly regulated ubiquitylated peptides expression, revealed the cell-type-specific concordance in ubiquitylation regulation upon BTK and SYK inhibition. These ubiquitylation modified proteins who bore the significantly regulated ubi-peptides in the samples were also found to be highly involved in gene regulatory processes.
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Jiang, Bingfu ; Wen, Xingjian ; Wu, Qingyan ; Bender, Daniela ; Carra, Gert ; Basic, Michael ; Kubesch, Alica ; Peiffer, Kai-Henrik ; Boller, Klaus ; Hildt, Eberhard
The N-terminus of the hepatitis B virus (HBV) large surface protein (LHB) differs with respect to genotypes. Compared to the amino terminus of genotype (Gt)D, in GtA, GtB and GtC, an additional identical 11 amino acids (aa) are found, while GtE and GtG share another similar 10 aa. Variants of GtB and GtC affecting this N-terminal part are associated with hepatoma formation. Deletion of these amino-terminal 11 aa in GtA reduces the amount of LHBs and changes subcellular accumulation (GtA-like pattern) to a dispersed distribution (GtD-like pattern). Vice versa, the fusion of the GtA-derived N-terminal 11 aa to GtD causes a GtA-like phenotype. However, insertion of the corresponding GtE-derived 10 aa to GtD has no effect. Deletion of these 11aa decreases filament size while neither the number of released viral genomes nor virion size and infectivity are affected. A negative regulatory element (aa 2–8) and a dominant positive regulatory element (aa 9–11) affecting the amount of LHBs were identified. The fusion of this motif to eGFP revealed that the effect on protein amount and subcellular distribution is not restricted to LHBs. These data identify a novel region in the N-terminus of LHBs affecting the amount and subcellular distribution of LHBs and identify release-promoting and -inhibiting aa residues within this motive.
We show strong overall and heterogeneous economic incidence effects, as well as distortionary effects, of only shifting statutory incidence (i.e., the agent on which taxes are levied), without any tax rate change. For identification, we exploit a tax change and administrative data from the credit market: (i) a policy change in 2018 in Spain shifting an existing mortgage tax from being levied on borrowers to being levied on banks; (ii) some areas, for historical reasons, were exempt from paying this tax (or have different tax rates); and (iii) an exhaustive matched credit register. We find the following robust results: First, after the policy change, the average mortgage rate increases consistently with a strong – but not complete – tax pass-through. Second, there is a large heterogeneity in such pass-through: larger for borrowers with lower income, a smaller number of lending relationships, not working for the lender, or facing less banks in their zip-code, thereby suggesting a bargaining power mechanism at work. Third, despite no variation in the tax rate, and consistent with the non-full tax pass-through, the tax shift increases banks’ risk-taking. More affected banks reduce costly mortgage insurance in case of loan default (especially so if banks have weaker ex-ante balance sheets) and expand into non-affected but (much) ex-ante riskier consumer lending, experiencing even higher ex-post defaults within consumer loans.
Recent research on the dynamics between attentional and memory processes have outlined the idea that applying control in a conflicting situation directly leads to enhanced episodic memory of the processed information. However, in spite of a small subset of studies supporting this claim, the majority of the evidence in the field seems to support the opposite pattern. In this study, we used a face–word Stroop task to enforce different control modes either from trial to trial or in an item-specific manner. Both manipulations of congruency proved to be effective in making participants’ responses to conflicting stimuli more efficient over time by applying a trial-specific control mode. However, these manipulations had no impact on memory performance on a surprise recognition memory test. To our knowledge, this is the first attempt at measuring the memory consequences of the application of specific control modes at the trial level. The results reported here call for caution and possibly reconceptualization of the relationship between cognitive control and memory.
Jivet, Ioana ; Scheffel, Maren ; Schmitz, Marcel ; Robbers, Stefan ; Specht, Marcus ; Drachsler, Hendrik
Highlights
• Transparency of design, reference frames and support for action were found to support students' sense-making of LA dashboards.
• The higher the overall SRL score, the more relevant the three factors were perceived by learners.
• Learner goals affect how relevant students find reference frames.
• The SRL effect on the perceived relevance of transparency depends on learner goals.
Abstract
Unequal stakeholder engagement is a common pitfall of adoption approaches of learning analytics in higher education leading to lower buy-in and flawed tools that fail to meet the needs of their target groups. With each design decision, we make assumptions on how learners will make sense of the visualisations, but we know very little about how students make sense of dashboard and which aspects influence their sense-making. We investigated how learner goals and self-regulated learning (SRL) skills influence dashboard sense-making following a mixed-methods research methodology: a qualitative pre-study followed-up with an extensive quantitative study with 247 university students. We uncovered three latent variables for sense-making: transparency of design, reference frames and support for action. SRL skills are predictors for how relevant students find these constructs. Learner goals have a significant effect only on the perceived relevance of reference frames. Knowing which factors influence students' sense-making will lead to more inclusive and flexible designs that will cater to the needs of both novice and expert learners.
Genotoxicity assessment is of high relevance for crude and refined petroleum products, since oil compounds are known to cause DNA damage with severe consequences for aquatic biota as demonstrated in long-term monitoring studies. This study aimed at the optimization and evaluation of small-scale higher-throughput assays (Ames fluctuation, micronucleus, Nrf2-CALUX®) covering different mechanistic endpoints as first screening tools for genotoxicity assessment of oils. Cells were exposed to native and chemically dispersed water-accommodated fractions (WAFs) of three oil types varying in their processing degree. Independent of an exogenous metabolic activation system, WAF compounds induced neither base exchange nor frame shift mutations in bacterial strains. However, significantly increased chromosomal aberrations in zebrafish liver (ZF-L) cells were observed. Oxidative stress was indicated for some treatments and was not correlated with observed DNA damage. Application of a chemical dispersant increased the genotoxic potential rather by the increased bioavailability of dissolved and particulate oil compounds. Nonetheless, the dispersant induced a clear oxidative stress response, indicating a relevance for general toxic stress. Results showed that the combination of different in vitro assays is important for a reliable genotoxicity assessment. Especially, the ZF-L capable of active metabolism and DNA repair seems to be a promising model for WAF testing.
Johann, Sarah ; Goßen, Mira ; Müller, Leonie ; Selja, Valentina ; Gustavson, Kim ; Fritt-Rasmussen, Janne ; Wegeberg, Susse ; Ciesielski, Tomasz Maciej ; Jenssen, Bjørn Munro ; Hollert, Henner ; Seiler, Thomas-Benjamin
In situ burning (ISB) is discussed to be one of the most suitable response strategies to combat oil spills in extreme conditions. After burning, a highly viscous and sticky residue is left and may over time pose a risk of exposing aquatic biota to toxic oil compounds. Scientific information about the impact of burn residues on the environment is scarce. In this context, a comprehensive ISB field experiment with approx. 1000L IFO 180 was conducted in a fjord in Greenland. The present study investigated the toxicity of collected ISB residues to early life stages of zebrafish (Danio rerio) as a model for potentially exposed pelagic organisms. The toxicity of ISB residues on zebrafish embryos was compared with the toxicity of the initial (unweathered) IFO 180 and chemically dispersed IFO 180. Morphological malformations, hatching success, swimming behavior, and biomarkers for exposure (CYP1A activity, AChE inhibition) were evaluated in order to cover the toxic response on different biological organization levels. Across all endpoints, ISB residues did not induce greater toxicity in zebrafish embryos compared with the initial oil. The application of a chemical dispersant increased the acute toxicity most likely due to a higher bioavailability of dissolved and particulate oil components. The results provide insight into the adverse effects of ISB residues on sensitive life stages of fish in comparison with chemical dispersant application.
Johé, Patrick ; Jaenicke, Elmar ; Neuweiler, Hannes ; Schirmeister, Tanja ; Kersten, Christian ; Hellmich, Ute
Rhodesain is the lysosomal cathepsin L-like cysteine protease of T. brucei rhodesiense, the causative agent of Human African Trypanosomiasis. The enzyme is essential for the proliferation and pathogenicity of the parasite as well as its ability to overcome the blood-brain barrier of the host. Lysosomal cathepsins are expressed as zymogens with an inactivating pro-domain that is cleaved under acidic conditions. A structure of the uncleaved maturation intermediate from a trypanosomal cathepsin L-like protease is currently not available. We thus established the heterologous expression of T. brucei rhodesiense pro-rhodesain in E. coli and determined its crystal structure. The trypanosomal pro-domain differs from non-parasitic pro-cathepsins by a unique, extended α-helix that blocks the active site and whose interactions resemble that of the antiprotozoal inhibitor K11777. Interdomain dynamics between pro- and core protease domain as observed by photoinduced electron transfer fluorescence correlation spectroscopy increase at low pH, where pro-rhodesain also undergoes autocleavage. Using the crystal structure, molecular dynamics simulations and mutagenesis, we identify a conserved interdomain salt bridge that prevents premature intramolecular cleavage at higher pH values and may thus present a control switch for the observed pH-sensitivity of pro-enzyme cleavage in (trypanosomal) CathL-like proteases.
Jonker, Hendrik R. A. ; Saxena, Krishna ; Shcherbakova, Aleksandra ; Tiemann, Birgit ; Bakker, Hans ; Schwalbe, Harald
Despite the great interest in glycoproteins, structural information reporting on conformation and dynamics of the sugar moieties are limited. We present a new biochemical method to express proteins with glycans that are selectively labeled with NMR‐active nuclei. We report on the incorporation of 13C‐labeled mannose in the C‐mannosylated UNC‐5 thrombospondin repeat. The conformational landscape of the C‐mannose sugar puckers attached to tryptophan residues of UNC‐5 is characterized by interconversion between the canonical 1C4 state and the B03 / 1S3 state. This flexibility may be essential for protein folding and stabilization. We foresee that this versatile tool to produce proteins with selectively labeled C‐mannose can be applied and adjusted to other systems and modifications and potentially paves a way to advance glycoprotein research by unravelling the dynamical and conformational properties of glycan structures and their interactions.
Joppe, Mirko ; D'Imprima, Edoardo ; Salustros, Nina ; Paithankar, Karthik Shivaji ; Vonck, Janet ; Grininger, Martin ; Kühlbrandt, Werner
Single-particle electron cryo-microscopy (cryoEM) has undergone a `resolution revolution' that makes it possible to characterize megadalton (MDa) complexes at atomic resolution without crystals. To fully exploit the new opportunities in molecular microscopy, new procedures for the cloning, expression and purification of macromolecular complexes need to be explored. Macromolecular assemblies are often unstable, and invasive construct design or inadequate purification conditions and sample-preparation methods can result in disassembly or denaturation. The structure of the 2.6 MDa yeast fatty acid synthase (FAS) has been studied by electron microscopy since the 1960s. Here, a new, streamlined protocol for the rapid production of purified yeast FAS for structure determination by high-resolution cryoEM is reported. Together with a companion protocol for preparing cryoEM specimens on a hydrophilized graphene layer, the new protocol yielded a 3.1 Å resolution map of yeast FAS from 15 000 automatically picked particles within a day. The high map quality enabled a complete atomic model of an intact fungal FAS to be built.
Endothelial dysfunction plays an important role in different pathological conditions, but whether endothelial cell death contributes to the development and progression of certain pathological conditions is rather unclear. Here we found that endothelial cells undergo cell death during pathologies such as LPS-induced sepsis and in models of hindlimb, renal and cardiac ischemia-reperfusion injury. Analyses of mice lacking endothelial key cell death regulators such as TAK1, RIPK3 and Caspase 8 gave us insight in the role of endothelial cell death in these pathological models. For example, increased endothelial necroptosis along with basal inflammation in lungs of TAK1ECKO mice affects susceptibility to LPS-induced sepsis and mortality, which correlated with elevated IFN-gamma and MIP-2 serum levels. Furthermore, we found that inhibition of RIPK3-mediated endothelial necroptosis could reduce the susceptibility of TAK1ECKO mice to LPS-induced sepsis and mortality. In ischemia or ischemia-reperfusion models, inhibition of RIPK3-mediated endothelial necroptosis did not reduce injury in the heart after ischemia, nor did it have any effect on organ function post-injury in the kidney or the heart. Inhibition of necroptosis also did not alter vascularization processes in hindlimb post-ischemia. Taken together, endothelial necroptosis contributes to increased sepsis severity and progression whereas inhibition of endothelial necroptosis can ameliorate susceptibility to sepsis in the absence of endothelial TAK1. Inhibition of endothelial necroptosis however does not play an important role during ischemia or ischemia-reperfusion induced organ injury.
Junghans, Arnd Rudolf ; Beyer, Roland ; Claußner, Jürgen ; Kögler, Toni ; Urlaß, Sebastian ; Bemmerer, Daniel ; Ferrari, Anna ; Schwengner, Ronald ; Wagner, Andreas ; Dietz, Mirco ; Frotscher, Axel ; Grieger, Marcel ; Hensel, Thomas ; Koppitz, Martina ; Ludwig, Felix ; Turkat, Steffen ; Nolte, Ralf ; Pirovano, Elisa ; Kopecky, Stefan ; Nyman, Markus ; Plompen, Arjan J. M. ; Schillebeeckx, Peter ; Borris, Erik ; Reifarth, René ; Veltum, Daniel ; Weigand, Mario ; Glorius, Jan ; Görres, Joachim ; Oberlack, Uwe ; Wenz, Daniel
Neutron total cross sections are an important source of experimental data in the evaluation of neutron-induced cross sections. The sum of all neutron-induced reaction cross sections can be determined with a precision of a few per cent in a relative measurement. The neutron spectrum of the photoneutron source nELBE extends in the fast region from about 100 keV to 10 MeV and has favourable conditions for transmission measurements due to the low instantaneous flux of neutrons and low gamma-flash background. Several materials of interest (in part included in the CIELO evaluation or on the HPRL of OECD/NEA) have been investigated: 197Au [1, 2], natFe [2], natW [2], 238U, natPt, 4He, natO, natNe, natXe. For gaseous targets high pressure gas cells with flat end-caps have been built that hold up to 200 bar pressure. The experimental setup will be presented including results from several transmission experiments and the data analysis leading to the total cross sections will be discussed.
Ziel dieser Untersuchung ist es, die Legitimität der Kriminalisierung des Glücksspiels in Brasilien zu hinterfragen. Dies geschieht mit besonderem Augenmerk auf das spezifische brasilianische Glücksspiel, das „Spiel der Tiere“ (Jogo do bicho), das Ende des 19. Jahrhunderts in der Stadt Rio de Janeiro, der Hauptstadt des damaligen kaiserlichen Brasiliens, entstand. Es handelt sich um eine Form des Glücksspiels, die sich in ganz Brasilien verbreitet hat und bereits Gegenstand mehrerer akademischer Studien in den Bereichen Anthropologie und Soziologie war. Das Verbot dieser Art von Glücksspiel, seine Kriminalisierung, seine große Beliebtheit und seine gesellschaftliche Toleranz sind jedoch Gründe dafür, dass das Spiel der Tiere im Besonderen und das Glücksspiel im Allgemeinen auch im juristischen Bereich, insbesondere im Strafrecht, ein bisher vernachlässigter Forschungsgegenstand von großem Interesse ist.
Das Hauptaugenmerk dieser Arbeit liegt auf der Analyse der Kriminalisierung des Glücksspiels, das in Brasilien seit über einem Jahrhundert unter freiem Himmel praktiziert wird. Bei dieser Analyse werden die Gründe für die Kriminalisierung und die Legitimität des Verbots in Frage gestellt. Zu diesem Zweck ist der Text, abgesehen von der Einleitung und der Schlussfolgerung, in sechs Kapitel unterteilt.
Kapitel 1 beschreibt die Geschichte des brasilianischen Tierspiels, die Ursprünge seines Verbots und seiner Kriminalisierung. In Kapitel 2 wird über die Wirklichkeit der Strafverfolgung in diesem „Kriminalitätsbereich“ berichtet. Kapitel 3 stellt den ent-sprechenden Straftatbestand des brasilianischen „Código Penal“ im Kontext der Systematik des brasilianischen Strafgesetzbuches vor. Kapitel 4 widmet sich zunächst den verfassungsrechtlichen Grenzen der Kriminalisierung, und danach einem Überblick über das deutsche Glücksspielverbot und die Glücksspielregulierung. Ergänzt wird diese Suche in Kapitel 5, in dem die Forschung das strafrechtliche Glücksspielverbot in den Kontext der Debatte über die Abgrenzung zwischen und den Zusammenhang von Recht und Moral. Im abschließenden Kapitel 6 wird das (strafrechtlich sanktionierte) Glücksspielverbot mit den klassischen Legitimations-anforderungen konfrontiert.
Was in der strafrechtlichen Literatur der ersten Hälfte des 20. Jahrhunderts zur Rechtfertigung des Verbots zu lesen ist, deutet auf einen großen Einfluss moralischer Argumente hin. Diese Argumente haben bis heute an Gewicht nicht verloren, auch wenn die Befürworter der Beibehaltung der Kriminalisierung versuchen, ihre letztlich moralistische Ideologie gegen das Glücksspiel mit Argumenten wie der Begleitkriminalität des Glückspiels zu verschleiern, die eher eine Folge als eine Ursache der Kriminalisierung ist.
Junker, Nina Mareen ; Kaluza, Antonia J. ; Häusser, Jan A. ; Mojzisch, Andreas ; Dick, Rolf van ; Knoll, Michael ; Demerouti, Evangelia
The relationship between exhaustion and work engagement has received considerable attention during the past decades. Although the theoretical proposition exists that work engagement may increase exhaustion over time, previous research has been mixed. Drawing on the transactional stress model and applying latent growth modeling, we aim to provide a more comprehensive picture of the work engagement–exhaustion relationship over time. In two longitudinal studies, with four measurement points each, we found consistent evidence that a higher initial work engagement related to increased exhaustion over time. Consistent with our hypotheses, a higher initial work engagement also related to less initial exhaustion, and increases in work engagement related to decreases in exhaustion over time. However, contrary to our expectations, a higher initial exhaustion related to elevated work engagement over time. In conclusion, our findings suggest that engaged employees are less exhausted but face a higher risk of exhaustion over time. At the same time, exhausted employees are less engaged, but they have the potential to become more so over time. The theoretical and practical implications of these findings will be discussed in this paper.
Junker, Nina Mareen ; Kaluza, Antonia J. ; Häusser, Jan ; Mojzisch, Andreas ; Dick, Rolf van ; Knoll, Michael ; Demerouti, Evangelia
The relationship between exhaustion and work engagement has received considerable attention during the past decades. Although the theoretical proposition exists that work engagement may increase exhaustion over time, previous research has been mixed. Drawing on the transactional stress model and applying latent growth modeling, we aim to provide a more comprehensive picture of the work engagement–exhaustion relationship over time. In two longitudinal studies, with four measurement points each, we found consistent evidence that a higher initial work engagement related to increased exhaustion over time. Consistent with our hypotheses, a higher initial work engagement also related to less initial exhaustion, and increases in work engagement related to decreases in exhaustion over time. However, contrary to our expectations, a higher initial exhaustion related to elevated work engagement over time. In conclusion, our findings suggest that engaged employees are less exhausted but face a higher risk of exhaustion over time. At the same time, exhausted employees are less engaged, but they have the potential to become more so over time. The theoretical and practical implications of these findings will be discussed in this paper.
Progressive bladder cancer growth is associated with abnormal activation of the mammalian target of the rapamycin (mTOR) pathway, but treatment with an mTOR inhibitor has not been as effective as expected. Rather, resistance develops under chronic drug use, prompting many patients to lower their relapse risk by turning to natural, plant-derived products. The present study was designed to evaluate whether the natural compound, sulforaphane (SFN), combined with the mTOR inhibitor everolimus, could block the growth and proliferation of bladder cancer cells in the short- and long-term. The bladder cancer cell lines RT112, UMUC3, and TCCSUP were exposed short- (24 h) or long-term (8 weeks) to everolimus (0.5 nM) or SFN (2.5 µM) alone or in combination. Cell growth, proliferation, apoptosis, cell cycle progression, and cell cycle regulating proteins were evaluated. siRNA blockade was used to investigate the functional impact of the proteins. Short-term application of SFN and/or everolimus resulted in significant tumor growth suppression, with additive inhibition on clonogenic tumor growth. Long-term everolimus treatment resulted in resistance development characterized by continued growth, and was associated with elevated Akt-mTOR signaling and cyclin-dependent kinase (CDK)1 phosphorylation and down-regulation of p19 and p27. In contrast, SFN alone or SFN+everolimus reduced cell growth and proliferation. Akt and Rictor signaling remained low, and p19 and p27 expressions were high under combined drug treatment. Long-term exposure to SFN+everolimus also induced acetylation of the H3 and H4 histones. Phosphorylation of CDK1 was diminished, whereby down-regulation of CDK1 and its binding partner, Cyclin B, inhibited tumor growth. In conclusion, the addition of SFN to the long-term everolimus application inhibits resistance development in bladder cancer cells in vitro. Therefore, sulforaphane may hold potential for treating bladder carcinoma in patients with resistance to an mTOR inhibitor.
Chronic treatment with the mTOR inhibitor, everolimus, fails long-term in preventing tumor growth and dissemination in cancer patients. Thus, patients experiencing treatment resistance seek complementary measures, hoping to improve therapeutic efficacy. This study investigated metastatic characteristics of bladder carcinoma cells exposed to everolimus combined with the isothiocyanate sulforaphane (SFN), which has been shown to exert cancer inhibiting properties. RT112, UMUC3, or TCCSUP bladder carcinoma cells were exposed short- (24 h) or long-term (8 weeks) to everolimus (0.5 nM) or SFN (2.5 µM), alone or in combination. Adhesion and chemotaxis along with profiling details of CD44 receptor variants (v) and integrin α and β subtypes were evaluated. The functional impact of CD44 and integrins was explored by blocking studies and siRNA knock-down. Long-term exposure to everolimus enhanced chemotactic activity, whereas long-term exposure to SFN or the SFN-everolimus combination diminished chemotaxis. CD44v4 and v7 increased on RT112 cells following exposure to SFN or SFN-everolimus. Up-regulation of the integrins α6, αV, and β1 and down-regulation of β4 that was present with everolimus alone could be prevented by combining SFN and everolimus. Down-regulation of αV, β1, and β4 reduced chemotactic activity, whereas knock-down of CD44 correlated with enhanced chemotaxis. SFN could, therefore, inhibit resistance-related tumor dissemination during everolimus-based bladder cancer treatment.
Jähnig, Sonja C. ; Baranov, Viktor ; Altermatt, Florian ; Cranston, Peter ; Friedrichs‐Manthey, Martin ; Geist, Juergen ; He, Fengzhi ; Heino, Jani ; Hering, Daniel ; Hölker, Franz ; Jourdan, Jonas ; Kalinkat, Gregor ; Kiesel, Jens ; Leese, Florian ; Maasri, Alain ; Monaghan, Michael T. ; Schäfer, Ralf B. ; Tockner, Klement ; Tonkin, Jonathan D. ; Domisch, Sami
A recent global meta‐analysis reported a decrease in terrestrial but increase in freshwater insect abundance and biomass (van Klink et al., Science 368, p. 417). The authors suggested that water quality has been improving, thereby challenging recent reports documenting drastic global declines in freshwater biodiversity. We raise two major concerns with the meta‐analysis and suggest that these account for the discrepancy with the declines reported elsewhere. First, total abundance and biomass alone are poor indicators of the status of freshwater insect assemblages, and the observed differences may well have been driven by the replacement of sensitive species with tolerant ones. Second, many of the datasets poorly represent global trends and reflect responses to local conditions or nonrandom site selection. We conclude that the results of the meta‐analysis should not be considered indicative of an overall improvement in the condition of freshwater ecosystems.
In Deutschland ist die Wohneigentumsquote innerhalb der OECD am zweitniedrigsten. Eine wichtige Rolle spielt dabei die Wohnungspolitik, die hierzulande Anreize für das Mieten schafft. Neue Studien zeigen, dass eine veränderte Politik die Wohneigentumsquote erhöhen und die Vermögensungleichheit verringern könnte.
Hintergrund. Ziel dieser Studie war es, zu bewerten, ob die Datenübertragung während peripherer endovaskulärer Eingriffe durch ein sprachgesteuertes, optisches Head-Mounted Display verwirklicht, und ob hierdurch der Arbeitsablauf der Intervention verbessert werden kann.
Methoden. Wir benutzten die Google Glass® Explorer Edition in Verbindung mit einer eigens entwickelten Glass App, um vorhandene Grafiken über die Datenbrille durch Sprachbefehle zugänglich zu machen. 40 Medizinstudenten im letzten Drittel des Medizinstudiums wurden in zwei Gruppen randomisiert.
Jeder Proband erhielt die Aufgabe eine PTA der A. femoralis superficialis an einem High-Fidelity-VR-Simulator (ANGIO-Mentor®, 3D Systems) durchzuführen. Während Gruppe A hierfür nötige Informationen über einen zusätzlich installierten Monitor erhielt, verwendete Gruppe B Google Glass®, um jeweilige Informationen durch zuvor definierte Sprachbefehle aufzurufen. Die objektive Bewertung der erbrachten Leistung erfolgte durch standardisierte Bewertungsbögen in dichotomer Nominalskalierung und durch die Messung der für die Aufgaben benötigten Zeit. Am Ende jeder Simulation erfolgte die subjektive Bewertung seitens der Probanden durch standardisierte Fragebögen mit 5-Level-Likert-Skalierung.
Ergebnisse. Eine maximale Punktzahl von 10 Punkten war erreichbar. Der in Gruppe A und Gruppe B gefundene Median lag bei 9 Punkten mit nicht signifikanten Abweichungen (p = 0,91). Die Gesamtdauer des Eingriffs betrug zwischen 12 und 14 Minuten. Gruppe B war unter Verwendung von Google Glass®, aufgrund technischer Schwierigkeiten mit der getesteten App, im Schnitt um 1:07 Minuten signifikant langsamer (p = 0,01). Dennoch konnte nachgewiesen werden, dass Google Glass® bei dem Transfer einfacher Informationen schneller oder zumindest gleichwertig gegenüber dem klassischen Monitoring war.
In diesem Kontext erachteten 92,5% der Probanden die Digitalisierung im klinischen Alltag als sinnvoll. 17 von 20 Teilnehmern (85%) empfanden die Handhabung von Google Glass® als einfach bis sehr einfach. Alle Teilnehmer waren der Ansicht, dass Augmented Reality bei peripheren endovaskulären Eingriffen im Katheterlabor nützlich sein könnte.
Schlussfolgerung. Google Glass® war dem klassischen Monitoring im Katheterlabor hinsichtlich der Gesamtinterventionszeit nur geringfügig unterlegen und behinderte den Arbeitsablauf während einer simulierten PTA der A. femoralis superficialis nicht. Unsere Studie offenbarte hierbei technische Schwierigkeiten bei der Genauigkeit der Spracherkennung und der Bildqualität von Google Glass®. Trotzdem konnten einzelne Aufgaben durch die Nutzung der Google Glass® signifikant schneller durchgeführt werden. Wir erwarten, dass nach Überwindung dieser technischen Probleme der Arbeitsablauf während endovaskulären Eingriffen mit einem optischen Head-Mounted Display verbessert werden kann.
Ein wahres Sammlungsjuwel der Bildhauerkunst des 20. Jahrhunderts findet sich im Museum der Fondation Pierre Gianadda im Wallis in der Schweiz: Neben der ständigen Skulpturenausstellung im Park, unter anderem mit Werken von Rodin, Miró und Niki de Saint Phalle, enthält die skurrile Sammlung auch Ausgrabungsreste aus gallo-romanischer Zeit, Oldtimer aus der Zeit der ersten Autos sowie wechselnde Kunstausstellungen im Museum.
Kaehler, Tanja ; John, Alexandra ; Jin, Tao ; Bolte, Michael ; Lerner, Hans-Wolfram ; Wagner, Matthias
Vicinally diiodinated polycyclic aromatic hydrocarbons (I2‐PAHs) are accessible from the corresponding diborylated B2‐PAHs through boron/iodine exchange. The B2‐PAHs have been prepared via twofold electrophilic borylation reactions templated by a vicinally disilylated benzene. Our protocol is applicable to fluorenes, acenes, annulated acenes, oligoaryls, and even [5]helicene. Using B2‐naphthalene as the example, we have shown that the reaction scope can, in principle, be expanded to include the synthesis of vicinally dibrominated and dihydroxylated PAHs. The usefulness of the building blocks provided by our method in the field of optoelectronic materials was demonstrated by the successful conversion of I2‐fluoranthene to the analogous doubly alkynylated fluoranthene emitter.
Kafkia, Eleni ; Andres-Pons, Amparo ; Ganter, Kerstin ; Seiler, Markus ; Jouhten, Paula ; Pereira, Filipa ; Zaugg, Judith B. ; Lancrin, Christophe ; Beck, Martin ; Patil, Kiran Raosaheb
Nucleic acid and histone modifications critically depend on central metabolism for substrates and co-factors. Although a few enzymes related to the formation of these required metabolites have been reported in the nucleus, the corresponding metabolic pathways are considered to function elsewhere in the cell. Here we show that a substantial part of the mitochondrial tricarboxylic acid (TCA) cycle, the biosynthetic hub of epigenetic modification factors, is operational also in the nucleus. Using 13C-tracer analysis, we identified activity of glutamine-to-fumarate, citrate-to-succinate, and glutamine-to-aspartate routes in the nuclei of HeLa cells. Proximity labeling mass-spectrometry revealed a spatial vicinity of the involved enzymes with core nuclear proteins, supporting their nuclear location. We further show nuclear localization of aconitase 2 and 2-oxoglutarate dehydrogenase in mouse embryonic stem cells. Together, our results demonstrate operation of an extended metabolic pathway in the nucleus warranting a revision of the canonical view on metabolic compartmentalization and gene expression regulation.
Das Spektrum kunstpädagogischer Thematisierungen von Inklusion ist – vergleichbar mit anderen Fachdidaktiken - wenig entfaltet. Die bisher vorliegenden Beiträge sind bisher kaum auf eine inklusionsbezogene Professionalisierung hin reflektiert. Die kontinuierliche Weiterentwicklung pädagogischer Professionalität zählt aber zu den grundlegenden Aufgaben der Kunstpädagogik und Bildungswissenschaft. Insbesondere da einzelne Zugänge der Professionalisierungsforschung theoretisch wie empirisch leistungsfähig sind und eine Reihe spezifischer Untersuchungen zu Aspekten der Professionalisierung hervorgebracht haben. Damit geht jedoch eine Zersplitterung der Professionalisierungsforschung in wenig miteinander kommunizierende Forschungslinien einher – diese Problematik lässt sich analog im kunstpädagogischen Diskurs wiederfinden. Unter den Erklärungsansätzen nehmen die verschiedenen Spielarten und Fortentwicklungen der struktur- und kompetenztheoretischen Argumentationen eine Schlüsselstellung ein, wobei sie jedoch eher Dissens als Konsens widerspiegeln. Infolgedessen wird das Konzept der Kontingenz im Beitrag als verbindendes Element herausgestellt und ein integrierender Vorschlag der Professionalisierung auf Basis von Kontingenzbearbeitung entwickelt.
Auf der Grundlage empirischer Rekonstruktion der Tiefenstrukturen der inklusionsbezogenen Professionalisierungsprozesse von angehenden Kunstlehrkräften (n=23) wird dazu ein Vorschlag unterbreitet, der auf zwei Pfeilern beruht: erstens der Analyse der Wahrnehmung und Deutung von Kontingenz im Professionalisierungsprozess und zweitens der Rekonstruktion von Mechanismen der Kontingenzbearbeitung. Das Moment der Kontingenzbearbeitung erweist sich zugleich als Ausgangs- wie Endpunkt entwicklungsgerichteter (kunst-)pädagogischer Professionalisierungsprozesse und als entscheidendes, anschlussfähiges Brückenglied zwischen den tradierten Argumentationslinien.
Der Beitrag arbeitet den Expertisebegriff für die inklusionsbezogene Professionalisierungsforschung auf und diskutiert diesen im Kontext des Desiderats nach einem übergreifenden Forschungsparadigma, das den strukturtheoretischen, den berufsbiografischen und den kompetenztheoretischen Ansatz verbindet. Die Überlegungen werden anhand von empirischen Befunden einer qualitativen (Teil-)Studie zur Expertise von Fortbildner*innen im Feld der inklusionsbezogenen Fortbildung exemplifiziert.
Kakeda, Aya ; Lien, Brenda ; Monaghan, Jonathan ; Lingo, Melissa Sixma ; Kesteleyn, An-Sofie ; Tammi, Maija
Seit der Mitte des 18. Jahrhunderts ist ein Steinensemble aus Frankfurt-Heddernheim/Nida bekannt, das aus einer 107 cm hohen Geniusstatue und einer zugehörigen Basis (Höhe 54 cm – Breite 50,5 cm – Tiefe 34,5 cm) aus Sandstein besteht. Die im Sockel eingeschlagene Inschrift datiert das Objekt durch die Angabe der amtierenden Konsuln in das Jahr 230 n. Chr. ...
Zielstellung: Es sollte im Rahmen dieser Arbeit geprüft werden ob (1) ein Zusammenhang zwischen einer radiologischen Beinlängendifferenz und einer veränderten Hüft- bzw. Kniegelenksbelastung bei Coxarthrosepatienten besteht. Des Weiteren galt es zu prüfen (2) ob die radiologisch-anatomische Beinachse bei Coxarthrosepatienten einen Einfluss auf die Gelenksbelastung von Hüfte und Knie habe und (3) ob sich in diesem Zusammenhang Unterschiede zwischen unilateral und bilateral betroffenem Patientenkollektiv darstellen ließe.
Hintergründe: Es konnte bereits gezeigt werden, dass Coxarthrosepatienten ein verändertes Gangbild aufweisen. Diese Veränderungen sind mitverantwortlich für eine veränderete Gelenkbelastung sowohl in Knie als auch Hüfte, sowohl im Vergleich zwischen betroffener und nicht betroffener Seite als auch im Vergleich zu hüftgesunden Normprobanden. Insbesondere bezüglich der Kniegelenksbelastung konnte bei den Betroffenen ein reduziertes Knieadduktionsmoment (KAM) während der Standphase nachgewiesen werden. Dies steht im Einklang mit der Beobachtung, dass Coxarthrosepatienten vermehrt eine laterale Kniearthrose auf der ipsilateralen Seite entwickeln. Coxarthrosepatienten zeigten darüber hinaus eine veränderte Beinachse, mit einer Tendenz hin zu einer Valgusfehlstellung. In wieweit insbesondere die proximale Beinachse einen Einfluss auf die alterierten Gelenkmomente hat, bleibt bislang jedoch offen. Zu bilateralen Patienten sind darüber hinaus nur wenige Daten vorliegend.
Methoden: Um die oben genannten Hypothesen zu prüfen wurden bei insgesamt 29 Patienten, bei welchen die Indikation für eine Hüfttotalendoprothese aufgrund einer fortgeschrittenen Coxarthrose gestellt wurde, eine instrumentelle Bewegungsanalyse sowie eine biplanare EOSRöntgenaufnahme, welche in diesem Zusammenhang die konventionelle präoperative Planungsaufnahme ersetzte, durchgeführt. Anschließend wurden die Daten, die aus der 3D EOS Rekonstruktion über die Beinachse gewonnen wurden, sowie die Ergebnisse der Bewegungsanalyse mit bereits zuvor erhobenen Normdaten sowie untereinander verglichen und statistisch analysiert.
Ergebnisse: Es zeigte sich, dass die Patienten eine bis auf MFA nicht von der Norm abweichende Beinachse hatten. Die bilateralen zeigten eine signifikant größere Beinlängendifferenz als die Norm, die unilateralen Patienten jedoch diesbezüglich keine Abweichung. Insgesamt zeigten die Patienten ein verändertes Gangbild, welches weitgehend den bereits in der Literatur beschriebenen Veränderungen entsprach.
Bezüglich der Gelenkmomente zeigte sich ein im Vergleich zur Norm erniedrigtes KAM 2, die übrigen Gelenkmomente zeigten keine Abweichungen von der Norm.
Es zeigten sich weder für die Beinachse noch für die Gelenkmomente signifikante Unterschiede zwischen unilateralem und bilateralem Patientenkollektiv.
Die unilateralen Patienten als gesamtes zeigten keine Korrelationen mit der absoluten Beinlängendifferenz. In einer unilateralen Subgruppe, in der die betroffene Seite länger war, konnte eine inverse Korrelation mit HAM 1 und HAM 2 gefunden werden.
KAM 1 und KAM 2 korrelierten signifikant mit allen Beinachsenparametern. In einer schrittweisen Regressionsanalyse mit HKA, FO und MFA konnten damit 68% der KAM 1 Alterationen und 57,5 % der Veränderungen von KAM 2 erklärt werden. HAM 1 und HAM 2 zeigten jeweils eine signifikante Korrelation mit MFA.
Schlussfolgerung: Die vorliegenden Ergebnisse zeigen, dass die Beinachse, insbesondere das Offset, einen Teil der Veränderungen der Kniegelenksbelastung erklären. Eine intraoperative Vergrößerung des Offsets und damit eine Varisierung der Beinachse könnte möglicherweise so zu einer Normalisierung der Kniegelenksbelastung führen.
Knee acoustic emissions provide information about joint health and loading in motion. As the reproducibility of knee acoustic emissions by vibroarthrography is yet unknown, we evaluated the intrasession and interday reliability of knee joint sounds. In 19 volunteers (25.6 ± 2.0 years, 11 female), knee joint sounds were recorded by two acoustic sensors (16,000 Hz; medial tibial plateau, patella). All participants performed four sets standing up/sitting down (five repetitions each). For measuring intrasession reliability, we used a washout phase of 30 min between the first three sets, and for interday reliability we used a washout phase of one week between sets 3 and 4. The mean amplitude (dB) and median power frequency (Hz, MPF) were analyzed for each set. Intraclass correlation coefficients (ICCs (2,1)), standard errors of measurement (SEMs), and coefficients of variability (CVs) were calculated. The intrasession ICCs ranged from 0.85 to 0.95 (tibia) and from 0.73 to 0.87 (patella). The corresponding SEMs for the amplitude were ≤1.44 dB (tibia) and ≤2.38 dB (patella); for the MPF, SEMs were ≤13.78 Hz (tibia) and ≤14.47 Hz (patella). The intrasession CVs were ≤0.06 (tibia) and ≤0.07 (patella) (p < 0.05). The interday ICCs ranged from 0.24 to 0.33 (tibia) and from 0 to 0.82 (patella) for both the MPF and amplitude. The interday SEMs were ≤4.39 dB (tibia) and ≤6.85 dB (patella) for the amplitude and ≤35.39 Hz (tibia) and ≤15.64 Hz (patella) for the MPF. The CVs were ≤0.14 (tibia) and ≤0.08 (patella). Knee joint sounds were highly repeatable within a single session but yielded inconsistent results for the interday reliability.
A glenohumeral internal rotation deficit (GIRD) of the shoulder, is associated with an increased risk of shoulder injuries in tennis athletes. The aim of the present study was to reveal the impact of 1) age, sex, specific training data (i.e. training volume, years of tennis practice, years of competitive play) and 2) upper extremity injuries on GIRD in youth competitive tennis athletes.
A cross-sectional retrospective study design was adopted. Youth tennis players (n = 27, 12.6 ± 1.80 yrs., 18 male) belonging to an elite tennis squad were included. After documenting the independent variables (anthropometric data, tennis specific data and history of injury), the players were tested for internal (IR) and external (ER) shoulder rotation range of motion (RoM, [°]). From these raw values, the GIRD parameters ER/IR ratio and side differences and TRoM side differences were calculated. Pearson’s correlation analyses were performed to find potential associations of the independent variables with the GIRD outcomes.
A significant positive linear correlation between the years of tennis training and IR side asymmetry occurred (p < .05). A significant negative linear relation between the years of tennis training and the ratio of ER to IR range of motion (RoM) in the dominant side (p < .05) was found. The analysis of covariance showed a significant influence of the history of injuries on IR RoM (p < .05).
Injury and training history but not age or training volume may impact on glenohumeral internal rotation deficit in youth tennis athletes. We showed that GIRD in the dominant side in youth tennis players is progressive with increasing years of tennis practice and independent of years of practice associated with the history of injuries. Early detection of decreased glenohumeral RoM (specifically IR), as well as injury prevention training programs, may be useful to reduce GIRD and its negative consequences.
Kalusche, Sarah ; Vanshylla, Kanika ; Kleipass, Franziska ; Gruell, Henning ; Müller, Barbara ; Zeng, Zhu ; Koch, Kathrin ; Stein, Stefan ; Marcotte, Harold ; Klein, Florian ; Dietrich, Ursula
In the absence of an active prophylactic vaccine against HIV-1, passively administered, broadly neutralizing antibodies (bnAbs) identified in some chronically infected persons were shown to prevent HIV-1 infection in animal models. However, passive administration of bnAbs may not be suited to prevent sexual HIV-1 transmission in high-risk cohorts, as a continuous high level of active bnAbs may be difficult to achieve at the primary site of sexual transmission, the human vagina with its acidic pH. Therefore, we used Lactobacillus, a natural commensal in the healthy vaginal microbiome, to express bn nanobodies (VHH) against HIV-1 that we reported previously. After demonstrating that recombinant VHHA6 expressed in E. coli was able to protect humanized mice from mucosal infection by HIV-1Bal, we expressed VHHA6 in a soluble or in a cell-wall-anchored form in Lactobacillus rhamnosus DSM14870. This strain is already clinically applied for treatment of bacterial vaginosis. Both forms of VHHA6 neutralized a set of primary epidemiologically relevant HIV-1 strains in vitro. Furthermore, VHHA6 was still active at an acidic pH. Thus, lactobacilli expressing bn VHH potentially represent an attractive vector for the passive immunization of women in cohorts at high risk of HIV-1 transmission.
Although researchers and practitioners increasingly focus on health promotion in organizations, research has been mainly fragmented and fails to integrate different organizational levels in terms of their effects on employee health. Drawing on organizational climate and social identity research, we present a cascading model of organizational health climate and demonstrate how and when leaders' perceptions of organizational health climate are linked to employee well‐being. We tested our model in two multisource studies (NStudy 1 = 65 leaders and 291 employees; NStudy 2 = 401 leader–employee dyads). Results showed that leaders' perceptions of organizational health climate were positively related to their health mindsets (i.e., their health awareness). These in turn were positively associated with their health‐promoting leadership behavior, which ultimately went along with better employee well‐being. Additionally, in Study 1, the relationship between perceived organizational health climate and leaders' health mindsets was moderated by their organizational identification. High leader identification strengthened the relationship between perceived organizational health climate and leaders' health mindsets. These findings have important implications for theory and practice as they show how the dynamics of an organizational health climate can unfold in organizations and how it is related to employee well‐being via the novel concept of health‐promoting leadership.
Culturally adapted cognitive behavioral therapy (CA-CBT) is a well-evaluated, transdiagnostic group intervention for refugees that uses psychoeducation, meditation, and stretching exercises. In the current study, we added problem-solving training to CA-CBT and evaluated this treatment (i.e., CA-CBT+) in a randomized controlled pilot trial with a sample of Farsi-speaking refugees. Participants (N = 24) were male refugees diagnosed with DSM-5 PTSD, major depressive disorder, and anxiety disorders who were randomly assigned to either a treatment or waitlist control (WLC) condition. Treatment components were adapted both to the specific cultural background and the current social problems of asylum seekers. Assessments were performed pretreatment, 12-weeks posttreatment, and 1-year follow-up. The primary treatment outcome was the General Health Questionnaire (GHQ-28); secondary outcome measures included the Posttraumatic Stress Disorder Checklist, Patient Health Questionnaire, Somatic Symptom Scale, World Health Organization Quality of Life, and Emotion Regulation Scale. Eleven of 12 participants were randomized to CA-CBT+ completed treatment. Based on intent-to-treat data, large between-group effect sizes were seen at posttreatment in the GHQ-28, d = 3.0, and for most secondary outcome measures. Improvements for individuals in the treatment group decreased at 1-year follow-up, but effect sizes demonstrated continued large improvements on all measures as compared to pretreatment levels. In summary, CA-CBT+ led to large improvements in general psychopathological distress and quality of life, which were maintained in the long term. In addition, the dropout rate was very low, with delivery in group format. Thus, problem-solving training appears to be a promising addition to CA-CBT.