Ablation of PGC1 beta prevents mTOR dependent endoplasmic reticulum stress response

Mitochondria dysfunction contributes to the pathophysiology of obesity, diabetes, neurodegeneration and ageing. The peroxisome proliferator-activated receptor-gamma coactivator-1 beta (PGC-1 beta) coordinates mitochondrial biogenesis and function as well as fatty acid metabolism. It has been suggested that endoplasmic reticulum (ER) stress may be one of the mechanisms linking mitochondrial dysfunction and these pathologies. Here we investigate whether PGC-1 beta ablation affects the ER stress response induced by specific nutritional and pharmacological challenges in the CNS. By using flow cytometry, western blot, real time PCR and several pharmacological and nutritional interventions in PGC-1 beta knock out and WT mice, we confirmed that PGC-1 beta coordinates mitochondria function in brain and reported for the first time that a) ablation of PGC-1 beta is associated with constitutive activation of mTORC1 pathway associated with increased basal GRP78 protein levels in hypothalamus and cortex of animals fed chow diet; and b) in animals fed chronically with high fat diet (HFD) or high protein diet (HPD). we observed a failure to appropriately induce ER stress response in the absence of PGC-1 beta, associated with an increase in mTOR pathway phosphorylation. This contrasted with the appropriate upregulation of ER stress response observed in wild type littermates. Additionally, inefficient in vitro induction of ER stress by thapsigargin seems result in apoptotic neuronal cell death in PGC-1 beta KO. Our data indicate that PGC-1 beta is required for a neuronal ER response to nutritional stress imposed by NED and HPD diets and that genetic ablation of PGC-1 beta might increase the susceptibility to neuronal damage and cell death. Published by Elsevier Inc.