Loss of Pla2r1 decreases cellular senescence and age‐related alterations caused by aging and Western diets

Author:

Massemin Amélie12,Goehrig Delphine12,Flaman Jean‐Michel12,Jaber Sara1,Griveau Audrey1,Djebali Sophia3ORCID,Marcos Elisabeth4,Payen Léa5,Marvel Jacqueline3,Parent Romain1,Adnot Serge4,Bertolino Philippe12,Rieusset Jennifer6,Tortereau Antonin7,Vindrieux David12,Bernard David12ORCID

Affiliation:

1. Centre de Recherche en Cancérologie de Lyon, Inserm U1052, CNRS UMR 5286, Centre Léon Bérard Université de Lyon Lyon France

2. Equipe Labellisée la Ligue Contre le Cancer 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

AbstractCellular 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.

Funder

Ligue Contre le Cancer

Publisher

Wiley

Subject

Cell Biology,Aging

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