ferrostatin-1 and dorsomorphin

Energy stress depletes ATP and induces cell death. Here we identify an unexpected inhibitory role of energy stress on ferroptosis, a form of regulated cell death induced by iron-dependent lipid peroxidation. We found that ferroptotic cell death and lipid peroxidation can be inhibited by treatments that induce or mimic energy stress. Inactivation of AMP-activated protein kinase (AMPK), a sensor of cellular energy status, largely abolishes the protective effects of energy stress on ferroptosis in vitro and on ferroptosis-associated renal ischaemia-reperfusion injury in vivo. Cancer cells with high basal AMPK activation are resistant to ferroptosis and AMPK inactivation sensitizes these cells to ferroptosis. Functional and lipidomic analyses further link AMPK regulation of ferroptosis to AMPK-mediated phosphorylation of acetyl-CoA carboxylase and polyunsaturated fatty acid biosynthesis. Our study demonstrates that energy stress inhibits ferroptosis partly through AMPK and reveals an unexpected coupling between ferroptosis and AMPK-mediated energy-stress signalling.

Topics: A549 Cells; Acetyl-CoA Carboxylase; AMP-Activated Protein Kinases; Animals; Cell Line, Tumor; Cyclohexylamines; Embryo, Mammalian; Energy Metabolism; Fatty Acids, Unsaturated; Ferroptosis; Fibroblasts; Gene Expression Regulation; Glucose; Humans; Iron; Kidney; Lipid Peroxidation; MCF-7 Cells; Mice; Mice, Transgenic; Phenylenediamines; Phosphorylation; Piperazines; Primary Cell Culture; Pyrazoles; Pyrimidines; Reperfusion Injury; Signal Transduction; Stress, Physiological