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Adapting protein fate for muscle function and fitness

Description du projet

Des muscles en bonne forme: le rôle des protéines

Des complexes protéiques orchestrés avec finesse, qui comprennent l’actine et la myosine, favorisent la contraction musculaire. Le maintien dynamique des taux protéiques (protéostase) est essentiel pour le tonus musculaire ainsi que pour la fonction musculaire indispensable au mouvement et aux frissons. Le projet PROTEOFIT, financé par l’UE, a entrepris de comprendre la manière dont les muscles détectent les taux protéiques et s’y adaptent. Les chercheurs étudient les mécanismes moléculaires de l’adaptation des muscles aux changements métaboliques, dans l’espoir de générer de précieuses connaissances sur la manière dont ces mécanismes sont perturbés chez les personnes atteintes d’obésité. L’identification des acteurs clés de ce processus devrait ouvrir la voie à de nouvelles interventions contre l’obésité et les troubles qui y sont associés.

Objectif

Muscle function is essential for motion, exercise, and shivering, whereas physical inactivity is causally related to reduced metabolic fitness in animal models and humans. A critical requirement for muscle function is that proteins are properly produced and, if necessary, degraded to adapt the proteome to meet metabolic demands. However, there is a fundamental, open gap in understanding how challenges to muscle proteostasis are sensed and how protein fate is subsequently adapted to enhance muscle function in exercise or, conversely, how it is compromised in obesity. I hypothesize that protein fate is highly adaptive and can be fine-tuned to promote proteostasis, the integrity of muscle cells, and metabolic health. Identifying novel key regulators of these mechanisms in muscle may hold great therapeutic promise for targeting metabolic fitness to combat obesity and associated disorders. In this innovative project I want to define new mechanisms of muscle adaptation in humans and preclinical mouse models, with the ultimate goal of using this knowledge to improve muscle function and fitness in obesity. I will identify exercise- and obesity-specific substrates of the proteasome by ubiquitomics in human and mouse muscle and define how the ubiquitination and turnover of these proteins dictates muscle cell function. In a complementary approach, I will use novel loss- and gain-of-function mouse models allowing for precise muscle-specific manipulation of Nfe2l1, an adaptive regulator of proteasomal protein degradation, to define the biological and therapeutic significance of this pathway for muscle function in exercise and obesity. In summary, this novel work will provide a transformative molecular understanding of muscle adaption to metabolic challenges and provide insight into how this translates into metabolic fitness and the development of obesity and associated disorders in humans.

Régime de financement

ERC-STG - Starting Grant

Institution d’accueil

LUDWIG-MAXIMILIANS-UNIVERSITAET MUENCHEN
Contribution nette de l'UE
€ 1 746 825,00
Adresse
GESCHWISTER SCHOLL PLATZ 1
80539 Muenchen
Allemagne

Voir sur la carte

Région
Bayern Oberbayern München, Kreisfreie Stadt
Type d’activité
Higher or Secondary Education Establishments
Liens
Coût total
€ 1 746 825,00

Bénéficiaires (1)