Tannine sind pflanzliche, polyphenolische Sekundärmetabolite mit Protein-präzipitierenden und –bindenden Kapazitäten, welche offenbar für die antinutritiven und gesundheitsschädlichen Wirkungen der Tannine verantwortlich sind. Jedoch dominieren in der Literatur die gesundheitsfördernden Beschreibungen, für die meist die antioxidative Kapazität verantwortlich gemacht wurde. Der etablierte Modelorganismus Caenorhabditis elegans wurde zur Analyse dieses Kontrastes ausgewählt. Zunächst wurden Lebensdauer und Stressresistenz der mit Tanninsäure und den Tanninbausteinen Gallussäure, Ellagsäure und Catechin behandelten Nematoden ermittelt. Das vermutete Vorliegen eines „Calorie Restriction“ (CR)-Effektes als auch einer hormetischen Dosis-Wirkungs-Beziehung wurde überprüft. Weiterhin wurden antimikrobielle und antioxidative Eigenschaften als potentielle Ursachen der Langlebigkeit untersucht und die Auswirkungen auf die Fitness und Genexpression analysiert. Die Einbeziehung verschiedener Alterungs-Theorien rundete die Analyse der Tanninwirkung ab. Alle Tannin-Substanzen konnten eine Lebensverlängerung erwirken, doch erstaunlicherweise erwiesen sich Langlebigkeit und Stressresistenz als individuelle, nicht zwangsläufig gekoppelte Parameter. Hormesis, CR-nachahmende Eigenschaften, antimikrobielle Kapazitäten als auch verschiedene stressrelevante Gene sind teilweise für die Lebensverlängerung verantwortlich. Die antioxidative Kapazität scheint jedoch irrelevant zu sein. Die differentielle Expression mehrerer hundert Gene durch Tanninsäure unterstreicht zudem die Komplexität der Wirkweise. Hinweise zur Bestätigung der „Disposable Soma Theory“, der „Mitohormesis“-Theorie und der „Green Theory of Ageing“ konnten zum Teil gefunden werden. Diese Arbeit zeigt die individuelle und kontrastreiche Wirksamkeit der Tannine auf. Sie unterstreicht, dass Tannine molekulare Regulatoren sind, welche nicht nur auf ihre antioxidative und antinutritive Kapazität reduziert werden sollten. / The polyphenolic tannins are plant-produced secondary metabolites with protein precipitating and binding capacities. This characteristic is seemingly responsible for antinutritional and harmful effects. However, health benefits have also been extensively described in the literature. Indeed, antioxidant properties are believed to be the reason for these beneficial effects. The established model organism Caenorhabditis elegans was chosen to examine this apparent contradiction. The nematodes were exposed to tannic acid and to the tannin building blocks gallic acid, ellagic acid, and catechin and the lifespan and stress resistance were determined. The presence of a calorie restriction (CR) effect and a hormetic dose-response-relationship was verified. Furthermore, antimicrobial and antioxidative capacities were assessed as possible causes of longevity and the impact on fitness parameters and gene expressions was analysed. The consideration of different ageing theories completed the analysis of the tannin action. All tannin-substances were able to prolong the lifespan but against all expectations, longevity and stress resistance were shown to be independent entities, which are not necessarily linked. Hormesis, CR-mimetic properties, antimicrobial capacities as well as several stress relevant genes are partly responsible for the life-extension. The antioxidant capacities, however, appeared to be irrelevant. The regulation of several hundred gene expressions by tannic acid underlined the complexity of the mode of action. Furthermore, the results partly confirm the “Disposable Soma Theory”, the “Mitohormesis Theory” and the “Green Theory of Ageing”. This work dissects the contrasting efficiency of the tannin family and underlines in particular, that tannins are molecular regulators, which should not be reduced to their antioxidative and antinutritional capacities

Cell polarity is required for asymmetric division, a mechanism to generate cell diversity by distributing fate determinants unequally to daughter cells. The establishment of polarity requires the evolutionarily conserved partitioning-defective (PAR) proteins as well as the actin cytoskeleton. In Caenorhabditis elegans one-cell embryos, the PAR proteins are segregated into an anterior (PAR-3, PAR-6) and a posterior (PAR-1, PAR-2) corticaldomain. The formation of PAR polarity correlates with anterior-posterior differences in the contractile activity of the cortex, known as "contractile polarity". It is thought that regulation of contractile polarity controls the establishment of PAR polarity, but detailed evidence to support this idea is lacking. To investigate how modulation of the actomyosin cytoskeleton affects polarity establishment, the acto-myosin cytoskeleton was perturbed by RNA-mediated interference (RNAi) of two Rho GTPases, CDC-42 and RHO-1. To examine how Rho GTPases are implemented in actin remodeling, it is important to analyze how their activity is controlled and how different activities affect polarity formation. The role of two putative Rho GTPase regulators, the Rho GTPase exchange factor (GEF) ECT-2 and the Rho GTPase activating protein (GAP) K09H11.3 were analyzed with respect to polarity formation. The formation of polarity was analyzed by using GFP-labeled proteins, and several different tracking methods were used to investigate the establishment of contractile and PAR polarity in more detail.This study demonstrates that both RHO-1 and CDC-42 are involved in polarity establishment in C. elegans embryos. But importantly, both act by different mechanisms. RHO-1 organizes the acto-myosin cytoskeleton into a contractile network, and therefore is essential for the formation of contractile polarity. The organization of the acto-myosin cytoskeleton is critical to ensure proper PAR protein distribution. Furthermore, a balance of RHO-1 activity by the GEF ECT-2 and the GAP K09H11.3 appears to be important for cortical contractility, for PAR protein domain size and for mutual exclusion of the PAR proteins. Although CDC-42 was shown to be a universal regulator of the actin cytoskeleton, CDC-42 acts downstream of contractile polarity. CDC-42 is required for linking PAR-6 to the cortex. In the absence of RHO-1 and ECT-2, PAR-6 and CDC-42 are not localized to the anterior cortex. This suggests that RHO-1, by organizing the actomyosin cytoskeleton into a contractile network, regulates the segregation of CDC-42 to the anterior cortex, and concomitantly PAR-6 localization. This study shows that the distribution of PAR is related to cortical activity and supports the model that the actin cytoskeleton plays an important role in polarity establishment.

La caractérisation des mécanismes moléculaires exacts de la signalisation de l'insuline est très importante pour comprendre, traiter et prévenir le diabète de type 2. Le deacetylase SIRT1 est une protéine récemment découverte qui est impliquée dans la régulation métabolique, comme dans la sécrétion de l'insuline et l'homéostasie glucidique. Un des activateurs de SIRT1, le resvératrol, a des effets bénéfiques sur la santé, dont une amélioration de la sensibilité à l'insuline et une durée de vie prolongée. Cependant, l'interaction exacte entre la signalisation de l'insuline, SIRT1 et le resvératrol n'est pas connue. Par conséquent j'ai étudié au cours de ma thèse l'impact du resvératrol et de SIRT1 sur la voie de signalisation de l'insuline, principalement dans des cellules musculaires mais aussi in vivo dans le modèle expérimentale du nématode C.elegans. J'ai pu montrer que le resvératrol est un inhibiteur class IA-spécifique de la PI3K. Le resveratrol inhibe aussi l'installation d'une insulino-résistance, peut-être par l'inhibition des protéines kinases comme JNK, diminuant ainsi la phosphorylation en sérine des IRS. Nous montrons aussi que SIRT1 intensifie la signalisation de l'insuline, probablement par l'interaction avec le complexe IRS-PI3K. L'interaction de SIR-2.1, l'homologue de SIRT1, avec la PI3K joue aussi un rôle important dans la régulation de la durée de vie de C.elegans / Characterisation of the exact molecular mechanisms of insulin signalling is of great importance in understanding, treating and preventing type 2 diabetes. The recently discovered deacetylase SIRT1 is implicated in several metabolic regulation mechanisms, including insulin secretion and glucose homeostasis. The SIRT1 activator resveratrol also has beneficial metabolic effects, including improved insulin sensitivity and prolonged lifespan. However, the exact interplay of insulin signalling, SIRT1 and resveratrol is not known. I have therefore studied the impact of resveratrol and SIRT1 on the insulin signalling pathway, mainly in muscle cells, but also in the living model C.elegans. This work has allowed me to show that resveratrol is an isoform-specific PI3K inhibitor. Resveratrol also inhibited instalment of insulin resistance, possible through inhibition of kinases like JNK thereby reducing the IRS serine phosphorylation. We also showed that SIRT1 potentiates insulin signalling, probably through interaction with IRS-PI3K. The interaction with SIR-2.1, the SIRT1 homolog, is important also in PI3K-mediated lifespan regulation in C.elegans

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