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Loss of Pla2r1 decreases cellular senescence and age-related alterations caused by aging and Western diets
Authors:Amélie Massemin  Delphine Goehrig  Jean-Michel Flaman  Sara Jaber  Audrey Griveau  Sophia Djebali  Elisabeth Marcos  Léa Payen  Jacqueline Marvel  Romain Parent  Serge Adnot  Philippe Bertolino  Jennifer Rieusset  Antonin Tortereau  David Vindrieux  David Bernard
Institution:1. Centre de Recherche en Cancérologie de Lyon, Inserm U1052, CNRS UMR 5286, Centre Léon Bérard, Université de Lyon, Lyon, France

Equipe Labellisée la Ligue Contre le Cancer, Lyon, France;2. Centre de Recherche en Cancérologie de Lyon, Inserm U1052, CNRS UMR 5286, Centre Léon Bérard, Université de Lyon, Lyon, France;3. Centre International de Recherche en Infectiologie, Inserm U1111, CNRS UMR5308, École Normale Supérieure de Lyon, Université de Lyon, Université Claude Bernard Lyon 1, Lyon, France;4. INSERM U955, Département de Physiologie - Explorations fonctionnelles, Hôpital Henri Mondor, AP-HP, FHU SENEC, Créteil, France;5. Laboratoire de Biochimie et Biologie Moléculaire, Centre Hospitalier Lyon Sud, Hospices Civils de Lyon, Pierre Bénite, France;6. CarMeN Laboratory, UMR INSERM U1060/INRA U1397, Lyon 1 University, Pierre bénite, France;7. VetAgro Sup, Interactions Cellules Environnement (ICE), Université de Lyon, Marcy l'Etoile, France

Abstract:Cellular senescence is induced by many stresses including telomere shortening, DNA damage, oxidative, or metabolic stresses. Senescent cells are stably cell cycle arrested and they secrete many factors including cytokines and chemokines. Accumulation of senescent cells promotes many age-related alterations and diseases. In this study, we investigated the role of the pro-senescent phospholipase A2 receptor 1 (PLA2R1) in regulating some age-related alterations in old mice and in mice subjected to a Western diet, whereas aged wild-type mice displayed a decreased ability to regulate their glycemia during glucose and insulin tolerance tests, aged Pla2r1 knockout (KO) mice efficiently regulated their glycemia and displayed fewer signs of aging. Loss of Pla2r1 was also found protective against the deleterious effects of a Western diet. Moreover, these Pla2r1 KO mice were partially protected from diet-induced senescent cell accumulation, steatosis, and fibrosis. Together these results support that Pla2r1 drives several age-related alterations, especially in the liver, arising during aging or through a Western diet.
Keywords:aging  cellular senescence  liver  Western diet
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