Distinct mitochondrial defects trigger the integrated stress response depending on the metabolic state of the cell

• Published in: eLife 2020-05, Vol.9
• Main Authors: Mick, Eran, Titov, Denis V, Skinner, Owen S, Sharma, Rohit, Jourdain, Alexis A, Mootha, Vamsi K
• Format: Article
• Language: English
• Subjects: Animals; Asparagine; Asparagine - metabolism; ATF4; ATP synthase; Biosynthesis; Cell cycle; Cell Line; Cellular stress response; Defects; Electron transport; Electron transport chain; GCN2; Gene expression; Genetics and Genomics; Human Biology and Medicine; Humans; Hyperpolarization; integrated stress response; Kinases; Metabolism; Metabolites; Metabolome - genetics; Metabolome - physiology; Mice; Mitochondria; Mitochondria - metabolism; Mitochondria - pathology; Mitochondrial DNA; Muscle Fibers, Skeletal - metabolism; Myoblasts; Myoblasts - metabolism; Myotubes; NAD - metabolism; NADH; Nature; Oxidation; Oxidation-Reduction; Oxidation-reduction reactions; p53; Phosphorylation; Proteins; Respiration; Scientific equipment industry; Stress, Physiological - genetics; Stress, Physiological - physiology; Transcriptome - genetics; Transcriptome - physiology
• ISSN: 2050-084X; 2050-084X
• DOI: 10.7554/elife.49178

Mitochondrial dysfunction is associated with activation of the integrated stress response (ISR) but the underlying triggers remain unclear. We systematically combined acute mitochondrial inhibitors with genetic tools for compartment-specific NADH oxidation to trace mechanisms linking different forms of mitochondrial dysfunction to the ISR in proliferating mouse myoblasts and in differentiated myotubes. In myoblasts, we find that impaired NADH oxidation upon electron transport chain (ETC) inhibition depletes asparagine, activating the ISR via the eIF2α kinase GCN2. In myotubes, however, impaired NADH oxidation following ETC inhibition neither depletes asparagine nor activates the ISR, reflecting an altered metabolic state. ATP synthase inhibition in myotubes triggers the ISR via a distinct mechanism related to mitochondrial inner-membrane hyperpolarization. Our work dispels the notion of a universal path linking mitochondrial dysfunction to the ISR, instead revealing multiple paths that depend both on the nature of the mitochondrial defect and on the metabolic state of the cell.