Cell Metabolism · 2022 · 191 citations · 57 references
Life SciencesBiochemistryCell BiologyCellular MetabolismMetabolismMitochondrial BiologyMitochondrial CardiomyopathyMitochondrial DiseaseMitochondrial DysfunctionMitochondrial PhysiologyMitochondrial Stress ResponsesOxidative StressAtf4 SignalingCytochrome C Oxidase AssemblyIntegrated Stress ResponseMitochondrial FragmentationMitochondrial Lipid PeroxidationOxidative Phosphorylation DefectsOxidative Phosphorylation DeficiencyOxphos Deficiency
mice aggravates cardiomyopathy. ISR inhibition impairs the cardiac glutathione metabolism, limits the selenium-dependent accumulation of the glutathione peroxidase Gpx4, and increases lipid peroxidation in the heart, ultimately culminating in ferroptosis. Our results demonstrate a protective role of the Oma1-Dele1-mediated ISR in mitochondrial cardiomyopathy and link ferroptosis to OXPHOS deficiency and mitochondrial disease.
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The CoQ oxidoreductase FSP1 acts parallel to GPX4 to inhibit ferroptosis
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