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Rafts: Rafts sind spezialisierte Domänen biologischer Membranen, die sich durch ihre spezifische Lipid- und Proteinzusammensetzung auszeichnen (zur Übersicht siehe Simons und Toomre, 2000). Die am besten beschriebenen Rafts sind die Caveolae, doch es gibt noch weitere weniger gut charakterisierte Rafttypen. Rafts werden verschiedene zelluläre Funktionen zugeschrieben wie z.B. gerichteter Transport von Membranproteinen, Endozytose und Signaltransduktion. Diese Funktionen erfüllen sie vornehmlich, indem sie verschiedene Proteine und Lipide bedingt durch ihre biophysikalischen Eigenschaften selektiv aufnehmen oder ausschließen. Viele Raftproteine sind über gesättigte Acylketten, wie Myristat oder Palmitat, oder einen GPIAnker mit der Membran assoziiert. Transmembranproteine, wie z.B. der EGFRezeptor, können jedoch auch in Rafts angereichert sein. Besonders an der Plasmamembran dienen Rafts als Signaltransduktionszentren, indem sie beteiligte Rezeptoren und Signalmoleküle konzentrieren.
Reggie-Proteine: Bei der Suche nach Proteinen, die bei der Regeneration von verletzten Sehnerven von Fischen hochreguliert werden, wurden Reggie-1 und Reggie-2 entdeckt (Schulte et al., 1997). Gleichzeitig wurden diese Proteine bei der Suche nach neuen Raftproteinen gefunden und als Flotillin-1 (=Reggie-2) und Flotillin-2 (=Reggie-1) bezeichnet (Bickel et al., 1997). Reggie-1 und -2 haben ein Molekulargewicht von 47 kDa und sind auf Aminosäuren-Basis zu 44% identisch. Homologe zu Reggie-1 wurden bislang in Mensch, Maus, Ratte und Fisch, wie auch in D. melanogaster gefunden. Die evolutionäre Konservierung der Reggies ist, mit beispielsweise 80% zwischen Ratte und Goldfisch, sehr hoch und weist auf eine wichtige Funktion hin, die Sequenzkonservierung verlangt. Reggie-1 wird ubiquitär exprimiert, wogegen Reggie-2 ein weniger verbreitetes Expressionsmuster aufweist. Reggie-1 ist vornehmlich an der Plasmamembran und an Endosomen lokalisiert. Die subzelluläre Lokalisation von Reggie-2 hängt vom Zelltyp ab...
Aim of the present study was the characterization of the RORa receptor (Retinoidrelated Orphan Receptor a). RORa is a member of the nuclear receptor family and is involved into the differentiation of Purkinje cells, inflammation, arteriosclerosis, and bone mineralization. Nuclear receptors are transcription factors and mediate biological responses within target cells to outer signals such as lipophilic hormones. They are involved in development, growth, differentiation, proliferation, apoptosis, and maintenance of homeostasis. Ligand binding, posttranslational modifications, and cofactor recruitment control their activity. Nearly all nuclear receptors share a common modular structure with an Nterminal A/B region, a DNA-binding domain (DBD) that is composed of two zinc finger motifs, a hinge region, and a C-terminal ligand-binding domain (LBD). The RORs comprise the subtypes RORa, RORb, and RORg, which are encoded by different genes. All isoforms of the respective subtypes only differ in their A/B domain. This study focused mainly on the exploration of the gene structure, expression, and subcellular distribution of RORa...
The melibiose permease (MelB) of E.coli functions as a secondary-active symporter by using the electrochemical H+, Na+, or Li+ gradient to accumulate, e.g., melibiose [review in Pourcher et al. 1990a]. The global and primary objective of this thesis was to apply pre-steady state methods for the investigation of reaction rates of individual steps in the cycle of MelB. Especially the melibiose binding induced transition was investigated by the solid-supported membrane (SSM) technique [Seifert et al. 1993] in combination with a rapid solution exchange system [Pintchovius and Fendler 1999] and with the Stopped-flow technique [Roughton 1934]. To approach this goal, either wild-type or mutated MelB were purified and reconstituted into liposomes as described [Pourcher et al. 1995]. Although the orientation of the proteins is a critical factor for the activity of MelB, it was, so far, unknown. To determine the orientation of the proteins in the liposomes, single Cys mutants R139C and R141C [Abdel-Dayem et al. 2003] were selectively labeled with 3-(N-maleimidylpropionyl)biocytin (MPB) and analyzed by SDS-PAGE and Western Blot. The assay indicated that most of the proteins are inside-out (ISO) oriented permitting to relate the pre-steady state electrical and fluorescence signals to the reverse transport activity of MelB. The melibiose induced electrical signal was investigated in wild-type MelB with the SSM technique. The transporter was activated by a substrate concentration jump, and transient currents were measured. When the transporter was preincubated with Na+ at saturating concentrations, a charge translocation in the protein upon melibiose binding could still be observed. This result demonstrates that binding of the uncharged substrate melibiose triggers a charge displacement in the protein. Further analysis showed that the charge displacement is neither related to extra Na+ binding to the transporter, nor to the displacement of already bound Na+ within MelB. Electrogenic melibiose binding is explained by a conformational change with concomitant displacement of charged amino acid side chains and/or a reorientation of helix dipoles. A kinetic model is suggested, in which Na+ and melibiose binding are distinct electrogenic processes associated with approximately the same charge displacement. Melibiose binding is fast in the presence of Na+ (k > 50 s-1). Furthermore, two previously identified transport deficient mutants of loop 4-5, R141C and E142C [Abdel-Dayem et al. 2002, Séry 2002], were purified and extensively studied with the SSM. Whereas the electrical signals from control cysteine-less mutant showed a bi-exponential time course of decay, those from R141C or E142C consisted of only a single fast exponential component, and the slow decaying component associated with substrate translocation was missing. The electrical signals evoked by a melibiose concentration jump in the presence of Na+ were much smaller than the corresponding signals in C-less MelB. Furthermore, R141C lost the stimulating effect of melibiose on Na+ binding. Steady-state Trp fluorescence spectroscopy revealed impaired conformational changes after melibiose binding in the mutants and fluorescence resonance energy transfer (FRET) measurements indicated that the mutants still show cooperative modification of their sugar binding sites by Na+. These data suggest that loop 4-5 contributes to the coordinated interactions between the ion- and sugar binding site and participates in conformational changes after melibiose binding that are essential for the subsequent obligatory coupled translocation of substrates. By using the Stopped-flow technique, three different approaches were followed. First, the intrinsic Trp fluorescence of MelB, known to increase upon melibiose binding [Mus-Veteau et al. 1995], revealed a signal with a T 1 of ~15 ms in C-less. This time constant is of the same order of magnitude as that determined with the SSM method suggesting that Trp fluorescence and electrical signal are related processes. Conformation for this assumption came from the fact that the activation energies Ea for both processes are similar (around 45 KJ/mol). Second, by using the fluorescent sugar analog Dns2-S-Gal, which monitors events close to the sugar binding site [Maehrel et al. 1998], a signal with a T 1 of ~18 ms was recorded upon Na+ addition. Finally, the fluorescent dye MIANS was used to selectively label the single Cys mutant E365C of loop 10-11. Stopped-flow measurements revealed a melibiose-induced fluorescent signal with a T 1 of 45 ms. Since electrical measurements with the MIANS-labeled E365C excluded the possibility that the label is responsible for the slower kinetics, the conformational change detected by the MIANS fluorescence was assigned to a slow transition in the cycle of MelB after melibiose binding. Ea was determined to be 96 KJ/mol corroborating, thus, the hypothesis of a different process. In conclusion, it was possible to correlate the electrical and fluorescence signals to partial reactions of the transport cycle and to determine their rate constants. According to this new model, the melibiose-induced signal detected with the Trp and electrical measurements corresponds to a step preceding the carriers’ reorientation (3 <-> 3*, k ~ 65s-1), and the melibiose-induced signal detected with the MIANS fluorescence to the reorientation itself (3* <-> 4, k ~ 20s-1).
Experimente zum radiativen Elektroneneinfang (REC, Radiative Electron Capture), der Zeitumkehrung der Photoionisation, wie er in Stößen hochgeladener, relativistischer Schwerionen mit leichten Gasatomen auftritt, ermöglicht einen einzigartigen Zugang zum Studium der Photonen-Materie-Wechselwirkung im Bereich extrem starker Coulombfeldern. So ist die REC-Strahlung im relativistischen Bereich zum einen geprägt durch das Auftreten von höheren elektrischen und magnetischen Multipolordnungen und zum anderen durch starke Retardierungseffekte. In Folge dessen wurde der REC-Prozeß in den vergangen Jahren sehr detailliert untersucht, wobei sich die experimentelle und theoretische Forschung auf die Emissionscharakteristik der REC-Photonen konzentrierte, wie z.B. auf Untersuchungen von Winkelverteilungen und Linienprofilen. Mittlerweile kann der REC-Prozeß als ein - selbst für die schwersten Ionen - wohlverstandener Effekt angesehen werden. Allerdings entzog sich den Experimenten bislang eine zur Beschreibung der Photonenmission wesentlich Größe, näamlich die Polarisation der Strahlung. Die lineare Polarisation der REC-Strahlung, wie sie in Stößen zwischen leichten Atomen und den schwersten, hochgeladenen Ionen vorhergesagt wird, war der Gegenstand der vorliegende Arbeit, in der es erstmals gelang, die diese für den konkreten Fall des Einfangs in die K-Schale von nackten Uranionen nachzuweisen und im Detail zu untersuchen. Die hierzu notwendigen experimentellen Untersuchungen erfolgten am Speicherring ESR der GSI-Darmstadt für das Stoßsystem U92+ -> N2 und für Projektilenergien, die im Bereich zwischen 98 und 400 MeV/u lagen. Besonders hervorzuheben ist der Einsatz eines segmentierten Germaniumdetektors, der speziell für den Nachweis linear polarisierter Strahlung im Energiebereich oberhalb 100 keV entwickelte wurde. Die lineare Polarisation der Strahlung wurde hierbei durch eine Analyse der Comptonstreuung innerhalb des Detektors gewonnen. Die durch eine präzise Analyse der Comptonstreuverteilungen gewonnenen Daten zeigen eine ausgeprägte lineare Polarisierung der REC-Strahlung in der Streuebene, die zudem eine starke Abhängigkeit als Funktion der Stoßenergie und des Beobachtungwinkels aufweist. Der detaillierte Vergleich mit nicht-relativistischen und relativistischen Vorhersagen ermöglichte darüberhinaus den Nachweis für das Auftreten starker relativistischer Effekte, die sich allerdings depolarisierend auswirken. Das Experiment wurde am internen Target des ESR-Speicherrings durchgeführt, wobei der Photonennachweis mittels mehrerer Ge(i)-Detektoren erfolgte, die die Ionen-Target-Wechselwirkungszone unter Beobachtungswinkeln zwischen nahe Null und 150 Grad einsahen. Alle Photonendetektoren wurden in Koinizidenz mit einem Teilchendetektor betrieben, um so die volle Charakteristik des REC-Prozesses zu erfassen, also den Einfang eines Targetelektrons in die nackten Uranionen (U92+) unter Emission eines Photons. Für den Polarisationsnachweis entscheidend war der Einsatz eines Germanium-Pixel-Detektors, der abwechselnd unter den Winkeln von 60 und 90 Grad betrieben wurde. Dieser Detektor verfügt über eine 4x4 Pixelmatrix (Pixelgröße: 7x7 mm), wobei die elektronische Information jedes Pixels (Energiesignale und schnelle Zeitsignale) separat registriert und aufgezeichnet wurde. Hierdurch war es möglich Ereignisse, die koinzident in zwei Pixeln erfolgten, zu detektieren und zu analysieren. Dies ist die eigentliche Voraussetzung für den Nachweis der linearen Polarisation bei hohen Photonenenergien, bei dem die Abhängigkeit des differenziellen Wirkungsquerschnitts für Comptonstreuung von der linearen Polarisation der einfallenden Photonen ausgenutzt wird (siehe Klein-Nishina Formel Eq. 2.7). Der Nachweis der Comptonstreuung erfolgt hierbei durch die Detektion des Compton-Rückstoßelektrons (deltaE) und des gestreuten Comptonphotons (hw'), die jeweils separat, aber koinzident in zwei unterschiedlichen Segmenten des Detektors nachgewiesen werden. Hier sei betont, dass für Germanium bereits ab Photonenenergien von ca. 160 keV die Absorption der Strahlung durch den Compton-Effekt über die Photoabsorption dominiert und somit das Ausnutzen des Compton-Effekts prinzipiell eine sehr effektive Technik ist. Der Auswertung der Datenfkam wesentlich zugute, dass der Germanium-Detektor über eine im Vergleich zu Szintillations- oder Gaszählern gute Energieauflösung von ca. 1.8 keV bei 122 keV verfügt. Somit kann durch Bilden der Summenenergie hw = hw' + deltaE für koinzidente Ereignisse die Energie des einfallenden Photons (hw) rekonstruieren werden und als zwingende Bedingung dafür herangezogen werden, dass es sich bei dem Ereignis im Detektor um ein Compton-Event gehandelt hat. Für den Fall linearer Polarisation ist eine wesentliche Aussage der Klein-Nishina-Formel, dass die maximale Intensität für die Compton gestreuten Photonen senkrecht zur Polarisationsebene zu erwarten ist. Tatsächlich zeigen bereits die während des Experiments aufgenommenen Rohdaten für den Fall der untersuchten REC-Strahlung, die durch den Einfang in die K-Schale des Projektils entsteht, dass es sich hierbei um eine stark polarisierte Strahlung handelt, wobei eine erhöhte Intensität für Comptonstreuung senkrecht zur Stoßebene (für den REC-Prozeß definiert durch die Ionenstrahlachse und den Impuls des REC-Photons) festgestellt wurde (vgl. Fig. 7.3). Zur genauen qualitativen Analyse der Meßdaten wurden alle möglichen Pixelkombinationen der (4x4) Detektorgeometrie ausgewertet, wobei jedoch koinzidente Ereignisse benachbarter Segmente ausgeschlossen wurden, um den hier vorhandenenen Einfluß elektronischer Übersprecher zu eliminieren. Zudem erfolgte die Analyse der Daten unter Berücksichtigung verschiedenster Effekte, die einen Einfluß auf die Nachweiseffizienzen für die Compton gestreuten Photonen haben könnten. An prominenter Stelle ist hier die Korrektur zu nennen, die durch die Detektordicke von 1,5 cm und der Pixelgröße von 7x7 cm2 hervorgerufen wird. Zu betonen ist hier, dass für die Auswertung nur relative Effizienzen eine Rolle spielen und so der Einfluß systematischer Fehler, hervorgerufen durch Effizienzkorrekturen, stark reduziert werden konnte (für eine so gewonnene, vollständige Compton-Streuverteilung sei auf Abbildung 9.1 verwiesen, in der die Intensitätsverteilung für Compton-Streuung dargestellt ist). Es sei auch hervorgehoben, dass der Nachweis der Polarisation durch Messungen von vollständigen Compton-Intensitätverteilung im Detektor erfolgte, was das hier diskutierte Experiment wesentlich von konventionellen Polarisationsexperimenten für harte Röntgen- und gamma-Strahlung unterscheidet. Üblicherweise wird in diesen Experimenten die Comptonstreuung ausschließlich in der Reaktionsebene und senkrecht dazu nachgewiesen. Generell weisen die in der vorliegenden Arbeit gewonnen Compton-Streuverteilungen für den K-REC-Prozeß ein ausgeprägtes Maxium senkrecht zur Reaktionsebene auf und bestätigen somit den bereits aus den Rohdaten abgeleiteten Befund, dass die Polarisationsebene der KREC Strahlung in der Reaktionsebene des Stosses liegt. In der Tat kann dieser Befund für alle Energien und Beobachtungswinkel bestätigt werden, die in dem hier diskutierten Experiment verwendet wurden. Hier sei zudem darauf hingewiesen, dass es durch die Erfassung der vollständigen Compton-Streuverteilung möglich war, die Orientierung der Polarisationsebene in Bezug auf die Stoßebene mit hoher Präzision zu erfassen. So konnte z.B. bei der Stossenergie von 400 MeV/u und dem Winkel von 90 Grad, die Orientierung der Comptonstreuverteilung in Bezug auf die Stoßebene zu ph=90 Grad bestimmt werden. Dieser Befund könnte für die Planung zukünftiger Experimente zum Nachweis polarisierter Ionenstrahlen entscheidend sein, da eine Abweichung von der ph = 90 Grad Symmetrie nur durch das Vorhandensein polarisierter Teilchen erklärt werden kann. Dieser Effekt, der in neuesten theoretischen Behandlungen im Detail untersucht wurde, stellt gleichsam einen neuen Zugang zur Bestimmung des Polarisationsgrads der Projektile dar. Hierdurch wird die Stärke der hier angewandten Technik verdeutlicht, die auf dem Einsatz eines ortsempfindlichen Germanium-Pixel- Detektors beruht. Die Bestimmung des genauen Polarisationsgrades für die K-REC-Strahlung erfolgte durch eine X2-Anpassung der Klein-Nishina-Formel an die experimentellen Daten. Die hieraus resultierenden Daten zeigen für alle Strahlenergien und Beobachtungsgwinkel eine starke Polarisation von etwa 80%, wobei die experimentelle Unsicherheit im 10% Bereich liegt. Letztere ist im wesentlichen auf die statistische Genauigkeit zurückzuführen. Die Daten wurden zudem eingehend mit theoretischen Vorhersagen verglichen. Die Theorie stützt sich auf eine vollständige relativistische Beschreibung des REC-Prozesses unter Verwendung exakter Wellenfunktionen für das Kontinuum und den 1s Zustand in wasserstoffartigem Uran. Typischer weise mußten bei den Rechnungen sowohl elektrische wie auch magnetische Multipolterme bis hin zu L=20 verwendet werden, um Konvergenz zu erreichen. Der Vergleich zeigt eine hervorragende Übereinstimmung zwischen Experiment und Theorie. Zudem verdeutlicht der Vergleich mit der ebenfalls diskutierten Vorhersage der nicht-relativistischen Dipolnäherung die Bedeutung relativistischer Effekte (vor allem das Auftreten höherer elektrischer und magnetischer Multipole), die für die Emission der REC-Strahlung bei hohen, relativistischen Energien und hohem Z charakteristisch sind. Offensichtlich wirken sich diese Effekte stark depolarisierend aus. Dass in der Tat eine Zunahme der depolarisierenden Effekte mit einer Zunahme der Strahlenergie verbunden ist, wird auch durch die Daten dokumentiert, die für den Beobachtungswinkel von 60 Grad als Funktion des Projektilenergie untersucht wurden. Die in der vorliegenden Arbeit gewonnenen Resultate für die Polarisation der REC-Strahlung ebenso wie die neuartige Experimenttechnik, die hierbei zum Einsatz kam, lassen für die nahe Zukunft eine Serie von weiteren Polarisations-Experimenten erwarten. Hierbei könnte der REC-Strahlung und deren Polarisation als Mittel zur Diagnostik und zum Nachweis des Polarisationsgrades gespeicherter Ionenstrahlen eine Schlüsselrolle zukommen. Als Detektorsysteme werden hierzu zwei-dimensionale Germanium- und Silizium-Streifen-Detektoren zum Einsatz kommen bzw. Kombinationen aus zweidimensionalen Silizium- und Germanium-Detektoren, sogenannte Compton-Teleskope. Diese Compton-Polarimeter, die gegenwärtig für neue Experimentvorhaben am ESR-Speicherring entwickelt werden, verfügen über eine wesentlich verbesserte Ortsauflösung (z.B. 1x1 mm2) und somit über eine wesentlich gesteigerte Nachweiseffizienz für die Comptonstreuung (ein bis zwei Größenordnungen). Hierdurch sollte es möglich sein, den für Polarisationexerperimente zugänglichen Energiebereich wesentlich auszudehnen, sodass selbst die charakteristische Strahlung der Schwerionen (ca. 50 bis 100 keV) für solche Experimente zugänglich wird.
The development of a drug product, beginning with the synthesis of the drug substance through approval for marketing, may take up to 15 years and a total amount of investment of up to half a billion Euro. After the discovery of a potential drug substance, many different investigations have to be performed: e.g. characterization of the physical-chemical properties, the pharmacological and toxicological profile and, especially relevant for this work, the development of the first dosage forms. After achieving these steps, first investigations in human studies can be carried out. After a positive assessment of the benefit to risk ratio, further investigations, such as food effects on the pharmacokinetics, multiple dosing studies and further studies on patients can be implemented. After successfully completing this second part the new drug product can be approved. With broader clinical experience it often becomes apparent that changes in relevant aspects of the formulation of the registered drug product e.g. excipients, concentration of the drug substance or excipient versus drug substance ratio, are necessary to optimise the therapy. This often leads to additional clinical investigations and a new registration, a procedure which is time and cost intensive. A possible way to reduce the financial and time investments, is to establish an appropriate in vivo- in vitro correlation (IVIVC). If it is possible to predict the in vivo performance of a drug product adequately with in vitro methods (dissolutions tests), it will no longer be necessary to perform additional clinical investigations. In this work, IVIVCs were investigated for three different drug substances and several different types of formulations.... ...Results of this work clearly show that successful IVIVCs can be achieved for the fasted state using biorelevant dissolution media. A prerequisite of achieving a good IVIVC is the availability of in vivo data of a reference product (i.v., oral solution or IR) tested within the same group of volunteers as the product of interest. Only with this procedure, one can obtain adequate IVIVCs for drug substances with high inter-individual variability of the plasma concentrations and with high first-pass metabolism. This work also shows that predictions of the in vivo behavior of a modified release dosage form after administration with a high fat meal are more difficult to obtain. This is mainly related to an absence of a medium, which could mimic the situation of the fed stomach adequately. Ensure plus®, which was chosen in this work, failed to simulate the fed stomach adequately in several cases; it suppressed the release of rosiglitazone from lipid formulations and led to rapid disruption of the HPMC-matrix of the 5-ISMN Geomatrix formulations. Future work should be directed towards optimization of the test media in the BioDis apparatus. This work clearly shows the inability of Ensure plus® to predict the in vivo performance of a drug under fed state conditions and indicates that alternative media must be developed. It is known that the pH of the stomach rises up to six after the intake of a meal. During the following hours the pH decreases until reaching the baseline value of approximately 1.8. One possibility of simulating the fed state stomach more precisely will be to divide the overall residence time into 4 different parts: 1. half a hour at pH 6 2. half a hour at pH 4 3. one hour at pH 3 4. two hours at pH 1.8 Another option is not only to modify the pH of the medium, but also to change its composition. During the decomposition of the food contents, the composition of the gastric juice changes, the ionic strength, the buffer capacity and the osmolarity rises, while the pH value decreases. A third possibility will be the addition of enzymes, mainly pepsin, lipases and amylases. Again, the quantity of the enzymes differs during the residence time of the food in the stomach. Highest quantities are expected in the first two hours after food intake and decreases in the remaining two hours. Another issue of this work was an assessment of the two dissolution apparatus, Paddle and BioDis. In general, the choice of the dissolution apparatus should be done primarily with respect to the solubility behavior of the drug substance. For high soluble drugs the USP apparatus II, Paddle, is sufficient (e.g. diltiazem or 5-ISMN). In cases of a poorly soluble drug (rosiglitazone), where the release strongly depends on the medium used, the USP apparatus III (BioDis) is favored, due to the advantage of simulating the GI-tract with a gradient of different dissolution media, each simulating one part of the GI-tract. In summary, the results of this work indicate that it is acurrently possible to predict fasted state behavior of a variety of controlled release products using in vitro tests. Prognoses was also made in terms of predicting food effects on the behavior of controlled release products, although it is clear that the media compositions will have to be revised to establish releiable predictive methods for the fed state.
Since its recognition as an endothelium-derived relaxing factor, the control and consequences of nitric oxide (NO) production have been investigated intensely. We know now that NO is not simply a vasodilator or regulator of smooth muscle tone but is a potent anti-platelet agent, neuromodulator and regulator of gene expression. NO is synthesized from the amino acid Larginine by a family of enzymes termed NO synthases (NOS). The ‘endothelial’ (eNOS or NOS III) and ‘neuronal’ (nNOS, NOS I or bNOS) NOS isoforms, which were named after the tissues in which they were first identified, are expressed constitutively and are generally regulated by Ca2+/calmodulin (CaM). Endothelium-derived NO is thought to be responsible for maintaining the vasculature in an anti-atherosclerotic state and a decrease in the bioavailability of NO (a state generally referred to as endothelial dysfunction) results in “proatherosclerotic” alterations in vascular gene expression. Recently it has become clear that the activity of eNOS is largely determined by its association with regulatory proteins as well as by the phosphorylation of the enzyme on serine, threonine and possibly tyrosine residues. Moreover, the enzyme can be “uncoupled” i.e. transformed from a NO generating to a superoxide (O2-)-generating enzyme, which would be expected to attenuate vasodilator responses and enhance vascular inflammation. The aim of this thesis was to study the consequences of phosphorylation on specific serine, threonine and tyrosine residues on the activity and intracellular localisation of eNOS and in particular to determine whether a phospho-switch for eNOS uncoupling exists. eNOS is phosphorylated under basal conditions and its serine phosphorylation can be enhanced following cell stimulation with hemodynamic stimuli such as cyclic stretch and fluid shear stress as well as by hormonal stimuli such as histamine and bradykinin. Our group has previously demonstrated the importance of Ser1177 in the activation of eNOS and here I set out to determine the relative importance of phosphorylation on Ser633 and Ser114. By generating point mutants in which serine was replaced by either alanine (nonphosphorylatable mutants) or aspartate (phosphomimetic mutants) it was observed that the activity of the S633D and S114A eNOS mutants exhibited an 2-fold increase over the activity of the wild-type enzyme or either of the S633/634A or S114D eNOS mutants as determined by monitoring the conversion of L-arginine to L-citrulline. eNOS is basally phosphorylated on Thr495 and stimulation of endothelial cells with Ca2+-elevating agonists generally results in the transient dephosphorylation of this residue. The latter is essential to allow the binding of calmodulin to the enzyme and is the actually initiating step in the generation of NO. Correspondingly, the T495A eNOS mutant can be activated at lower Ca2+ and calmodulin concentrations than the T495D mutant. However, some eNOS mutants (T494A/S1177D and T495A) showed an enhanced ability to generate O2- in a NOS inhibitor-sensitive manner suggesting that the phosphorylation of the enzyme may also play a role in the uncoupling process. To determine the physiological relevance of eNOS dephosphorylation on Thr495 we assessed the consequences of treating cells with oxidised low-density lipoprotein (ox-LDL) on eNOS phosphorylation as well as on the eNOS-dependent generation of NO and O2-. Oxidised LDL concentration- and time-dependently decreased phosphorylation of eNOS on Thr495 and led to a concomitant decrease in cellular levels of cyclic GMP and an enhanced production of O2 - compared to cells treated with native LDL. Alterations in the activity of protein kinase C (PKC) were related to the change in eNOS Thr495 phosphorylation. There was not only the basal activity of PKCα inhibited by ox-LDL but the PKC activator phorbol-12-myristate-13-acetate also failed to elicit the phosphorylation of Thr495 in ox-LDL-treated endothelial cells. The dephosphorylation of eNOS on Thr495 in response to the addition of ox-LDL was not associated with an increase in the binding of calmodulin to eNOS, an association usually necessary for the activation of eNOS. Moreover, following treatment with ox-LDL for 24 hours eNOS was no longer detected at the plasma membrane but was redistributed to the cytosol indicating that ox-LDL may disrupt the eNOS signalling complex or signalosome. To date the role played by the tyrosine phosphorylation of eNOS in the regulation of its activity or intracellular association is controversial. However, during the preparation of this thesis we have been able to demonstrate a link between the tyrosine phosphorylation of eNO and the activation of the tyrosine kinases Src and PYK2. The application of fluid shear stress to endothelial cells resulted in the activation of Src and PYK2 as well as in the association of PYK2 with eNOS. Co-expression of eNOS and PYK2 led to the putative identification of Tyr657 as a potential modulatory site. Mutating eNOS at Tyr657 to Asp or Glu resulted in the localisation of the mutant eNOS predominantly in the cytoskeleton and also in a complete inactivation of the enzyme. The Y657F mutants, on the other hand, did not demonstrate any marked alteration in the activity when compared with the wild-type eNOS. However, the In conclusion, the results describe in this thesis indicate that eNOS is regulated by phosphorylation at multiple sites. Depending on the phosphorylation site involved phosphorylation can inhibit or activate NO production or even uncouple the enzyme so that it generates O2-. While the phosphor-status of eNOS on Ser114 and Ser633 influenced NO release they did not contribute to O2 - production and the dephosphorylation of Thr495 seems sufficient to uncouple eNOS. Cell treatment with ox-LDL, which is known to increase eNOS-derived O2- output was correlated with a dephosphorylation of Thr495 as well as a decrease in the activity of the kinase that phosphorylates this site i.e., PKCα. The phosphorylation status of all the eNOS serine and threonine residues studied however did not influence the ability of the enzyme to dimerise, indicating that contrary to previously published reports the eNOS dimer is highly stable in endothelial cells. The tyrosine phosphorylation of eNOS was not initially expected to play a determinant role in the regulation but rather to facilitate the docking of associated regulatory proteins. However, Tyr657 seems to play a critical role in the generation of NO as its mutation resulted in the generation of a completely inactive enzyme as well as in an apparent intracellular mislocalisation of the protein. The physiological relevance of these findings remain to be further elucidated.
Amblyopia is a developmental disorder of the visual system that leads to reduced vision in one or both eyes. People suffering from amblyopia show different perceptual deficits like reduced contrast sensitivity, reduced or no stereopsis, spatial uncertainty, and spatial and temporal distortions when viewing with the amblyopic eye. In the following thesis, different psychophysical methods are used to investigate anomalous perception of amblyopic participants in detail with the main focus on the perception of temporal instability. In the qualitative experimental paradigms it is shown that temporal instability is mainly perceived by strabismic and strabismic-anisometropic amblyopes. The temporal deficits occur only at spatial frequencies higher than 1.6 c/deg, and are perceived in addition to the spatial distortions. Illusory colours sometimes accompany the temporal distortions. There seems to be a relationship between crossed hand and eye dominance and the perception of temporal instability. In the quantitative experiments it is shown that temporal instability in amblyopic perception has a negative impact on the performance in psychophysical tasks. Amblyopes perceiving temporal instability show enhanced spatial uncertainty and spatial distortions for different types of stimulus presentation (auditive vs. visual) when compared to amblyopes without temporal instability. This might be due to deficits in auditive-visual mapping. These deficits in auditory-to-visual mapping suggest an impairment of the dorsal “where” pathway. Thus, it might be that amblyopes with temporal distortions have deficits in the dorsal pathway that come up in addition to the known deficits of the ventral “what” pathway and are related to the perception of temporal instability. The different results of the experiments found in this thesis seem to confirm this hypothesis. Studies using functional imaging techniques might be appropriate for a further investigation of amblyopic deficits involving the dorsal pathway.
The Kaon-Spectrometer (KaoS) at the heavy-ion synchrotron (SIS) at the Gesellschaft für Schwerionenforschung (GSI) in Darmstadt has been used to study production and propagation of K+ and K- mesons from Au+Au collisions at a kinetic beam energy of 1.5 AGeV. This energy for K+ mesons is close to the corresponding production threshold in binary nucleon-nucleon collisions and far below for K- mesons. The azimuthal angular distributions of particles as a function of the collision centrality and particle transverse momenta have been measured. The properties of strange mesons are expected to be modified by the in-medium meson-baryon potential. Theoretical calculations show that the superposition of the scalar and vector potentials leads to a small repulsive K+N and a strong attractive K-N potential. Additionally, the interaction of kaons and antikaons with nuclear matter is different. The strangeness conservation law inhibits the absorption probability of K+ mesons as they contain an s-quark. K- mesons, however, interact with nucleons via strangenessexchange (K- + N ->Y + pion, where Y = lambda, sigma). Moreover, the reverse process (pion + Y -> K- + N) is the dominant production mechanism of K- mesons at SIS energies. The azimuthal angular emission patterns of kaons are expected to be sensitive to the in-medium potentials. An enhanced out-of-plane emission of K+ mesons was observed in Au+Au reactions at 1.0 AGeV and 1.5 AGeV, and also in Ni+Ni at 1.93 AGeV. The out-of-plane emission of K+ mesons in Au+Au reactions at 1.0 AGeV was interpreted as a consequence of a repulsive K+N potential in the nuclear medium, however, recent transport calculations show that the emission patterns obtained in Au+Au at 1.5 AGeV and Ni+Ni at 1.93 AGeV are additionally influenced by the re-scattering of kaons. For K- mesons the calculations predict an almost isotropic emission pattern due to the attractive K-N potential which counteracts the absorption of K- mesons in the spectator fragments. In Ni+Ni collisions at 1.93 AGeV the azimuthal distribution of K- mesons has been found to be isotropic. In this case, however, the spectators are rather small and have large relative velocities. In addition, the delay of antikaon emission due to strangenessexchange reaction minimizes the interaction with the spectators. As a consequence the sensitivity of the K- meson emission pattern to the K-N in-medium potential is reduced. In Au+Au collisions we found a dependence of the K- meson azimuthal emission pattern on the transverse momentum. The antikaons registered with pt < 0.5 GeV/c are preferentially emitted in the reaction plane and the particles with pt > 0.5 GeV/c show strong out-of-plane enhancement. The emission patterns of K- can be explained in terms of two competing phenomena: one of them is indeed the influence of the attractive K-N potential, however, the second one originates from the strangeness-exchange process.
Soluble guanylyl cyclase (sGC) is a cytosolic enzyme producing the intracellular messenger cyclic guanosine monophosphate (cGMP) on activation with nitric oxide (NO) which leads to the activation of GMP dependent protein kinases and to vasodilation. NO signaling may be affected by altered expression of sGC subunits, as has been shown in different pathological and physiological conditions and developmental stages. The molecular mechanisms underlying altered sGC expression in these and other conditions have not yet been revealed. Gene expression can also be regulated at the level of mRNA through alterations in translational efficiency and in mRNA stability. HuR (Human R) is a ubiquitously expressed member of the embryonic lethal abnormal vision (ELAV) family of RNA-binding proteins. Among other RNAs, there has been recent evidence that the expression of sGC is subject to post-transcriptional regulation by HuR. It has been shown that chronic hypertension induces changes in HuR expression and activity, which account for decreased sGC expression and activity in the aorta of hypertensive rats. This thesis should study was performed in an effort to provide some insight to the transcriptional and post-transcriptional regulation of sGC expression in a mammal, the rat. We investigated rat sGC alpha-1 transcriptional regulation in rat lung fibroblast (RLF-6) cells. The 3000bp 5' upstream region of the alpha-1 sGC gene was isolated and analyzed for promoter activity by using luciferase reporter constructs- Alpha3000 (with -2794 bp), Alpha1100 (-1092 bp), Alpha350 (-346 bp) and Alpha200 (-200 bp). The promoter activity was the highest in the 200bp construct (about 6-fold higher than Alpha3000) suggesting that this fragment contains all the crucial elements necessary to support basal transcription of the alpha-1 sGC gene. Analysis of the 200 bp of the 5’ UTR of the alpha-1 gene was performed using the MATINSPECTOR V2.2 software for putative transcription factors. The constructs containing the deleted sites for NFY and Sp1 showed a significant decrease in constitutive promoter activity by almost 80% and 60% respectively, implying that these transcription factors are crucial elements in the basal expression of the of sGC alpha-1 subunit. Treatment of RLF-6 cells with genistein 50 microM and mithramycinA 100 nM, known to inhibit the NFY and Sp1 binding to DNA respectively, reflected the same effects. Furthermore the cGMP content of the cells was significantly reduced by both inhibitors, almost completely by genistein, and by about 40 % by mithramycinA. Electrophoretic mobility-shift assay (EMSA) clearly showed the formation of multiple complexes with the biotinylated ODN (decoy oligodeoxynucleotide) probes for NFY and Sp1 when incubated with RLF-6 nuclear extract. A “supershift” observed in the presence of antibodies to the individual transcription factors confirmed that these factors were present in the shifted band, indeed. NFY and Sp1 are instrumental in several physiological and pathophysiological effects mediated by several growth factors in smooth muscle cells. Thus the regulation of the promoter, in response to serum, was also analysed. 10% foetal calf serum led to decreased alpha-1 sGC level as shown by western blots performed with rat aorta. Decreased sGC alpha-1 mRNA expression was observed in RLF-6 cells and cultured rat aortic smooth muscle cells incubated with FCS for 24 hours. This decrease was reflected in the promoter activity in RLF-6 cells using both Alpha3000 and Alpha200 constructs confirming that the regulation took place at promoter level. EMSA performed with nuclear extracts from FCS treated RLF-6 cells led to diminished binding to NFY, but to an enhanced binding to Sp1 site. We concluded that the factors Sp1 and NFY (the sites overlapping) compete for binding, and in the presence of FCS, it is Sp1 that binds stronger, and hence results in diminishing promoter activity. In order to delineate the post-transcriptional regulation of sGC alpha-1 subunit, studies were performed to demonstrate the regulation of expression of the mRNA stabilizing protein HuR. It has been observed that exposure of isolated rat aortic segments to the activator of adenylyl cyclase, forskolin, strongly reduced sGC alpha-1/beta-1 and HuR protein and mRNA expression in a time-dependent and actinomycin D-sensitive fashion. Transcription factor decoy approach proved that the cAMP-induced down-regulation of HuR is mediated by the activation of AP-1. It has been established that HuR stabilises the sGC alpha-1 and beta-1 mRNA. However the pathway underlying this regulation remains unknown. In order to identify the mechanism of this regulation, we looked for HuR interacting proteins employing the yeast two hybrid assay. The enzyme of the polyamine catabolic pathway spermidine/spermine N1-acetyltransferase (SSAT) was found to interact with the hinge region of HuR. This interaction was confirmed by performing immunoprecipitation and GST-pulldown experiments. A direct effect of these proteins on each other’s biological activity was not visible as tested through the SSAT activity assay and HuR gel shift. It might be possible that SSAT-mediated modulation of local polyamine concentrations enhances/reduces HuR activity and sGC expression to affect cell proliferation. In summary, this study represents an analysis of the rat sGC alpha-1 promoter regulation in rat fibroblast cells and identifies NFY and Sp1 as important factors in sGC alpha-1 expression. It also gives first evidence of sGC regulation at the transcriptional level in response to an external stimulus, and proposes the possible mechanism. It also identifies SSAT as a HuR interacting protein. These might have implications in the various pathophysiological conditions where sGC plays an important role.
The generation of O2- by NADPH oxidaes was mainly attributed to immune cells that kill invading bacteria or cancer cells. But importantly, in the past several years, several homologs of the catalytic subunit gp91phox (Nox2) of the phagocytic NADPH oxidase have been identified in non-immune cells and tissues. Superoxide production derived from NADPH oxidaes has been shown to play a role not only in host defense but also in defined signaling cascades mediating growth and apoptosis. The aim of this work was to study the expression and the regulation of the”new” Nox isoforms in rat renal mesangial cells (MC). In particular the following results were achieved. 1) mRNA’s for both Nox1 and Nox4 were detected by RT-PCR. 2) Nox1 mRNA levels were increased upon exposure to basic fibroblast growth factor (bFGF), platelet-derived growth factor (PDGF) and fetal calf serum (FCS) in a time- and dose-dependent manner. Exposure of MC to bFGF and FCS increased also basal production of reactive oxygen species (ROS) by MC. By contrast, Nox4 mRNA levels were not significantly affected by bFGF treatment, but were markedly down-regulated by PDGF and FCS. 3) To study the regulation of Nox1 on the protein level, an anti-Nox1 antibody was generated and characterized using affinity chromatography. Up-regulation of Nox1 expression by growth factors was confirmed also on the protein level. 4) Based on the already known cDNA sequence for Nox1, the transcriptional start site was determined by the “gene RACE” technique. 2547 bp of the genomic sequence of the 5´-flanking region of the Nox1 gene were cloned and sequenced using the „Genome-Walking“ method. To study the regulation of Nox1 transcription functional Nox1 promoter/luciferase fusions were be established. MC were transiently transfected with different promoter/luciferase constructs and stimulated with growth factors. By measuring luciferase activity it was determined that growth factors induced the Nox1 transcription and that the Nox1 core promoter is sufficient for the activation. 5) By measurement of superoxide radicals and analysis of Nox1 mRNA expression by quantitative RT-PCR (TaqMan) as well as protein level by Western blotting it could be shown that treatment of MC with NO donors inhibited the expression of Nox1 in a time- and dose-dependent manner. Moreover, using activators and inhibitors of the soluble guanylyl cyclase (sGC) it could be shown, that the activation of sGC mediates the effect of NO on Nox1 expression. However, NO had no inhibitory effect on Nox1 promoter activity. Experiments with the inhibitor of transcription, actinomycin D, suggest that NO-mediated regulation of Nox1 is triggered probably via post-transcriptional mechanisms. Nox4 is regulated on the mRNA levels in a similar manner as Nox1. 6) To analyze the sub-cellular localization of the Nox isoforms, coding sequences for Nox1 and Nox4 were fused together with green fluorescent protein into the pEGFP-N1 demonstrated that both isoforms are localized predominantly in the plasma membrane, but also in the perinuclear region and cytoplasm. However, the localization of Nox1 in the plasma membrane was more pronounced. 7) In addition to Nox1 and Nox4, mRNA of the newly identified NOXA1 that is a homolog of the p67phox subunit of NADPH oxidase was detected in MC by RT-PCR.