
Ferroptosis is a form of iron-dependent regulated cell death driven by uncontrolled lipid peroxidation. Mitochondria are double-membrane organelles that have essential roles in energy production, cellular metabolism, and cell death regulation. However, their role in ferroptosis has been unclear and somewhat controversial. In this Perspective, I summarize the diverse metabolic processes in mitochondria that actively drive ferroptosis, discuss recently discovered mitochondria-localized defense systems that detoxify mitochondrial lipid peroxides and protect against ferroptosis, present new evidence for the roles of mitochondria in regulating ferroptosis, and outline outstanding questions on this fascinating topic for future investigations. An in-depth understanding of mitochondria functions in ferroptosis will have important implications for both fundamental cell biology and disease treatment.
Amino Acid Transport System y+, Ubiquinone, Iron, Oxidants, Phospholipid Hydroperoxide Glutathione Peroxidase, Glutathione, Mitochondria, Small Molecule Libraries, Gene Expression Regulation, Perspective, Ferroptosis, Humans, S100 Calcium-Binding Protein A4, Lipid Peroxidation, GTP Cyclohydrolase, Reactive Oxygen Species, Cells, Cultured, Signal Transduction
Amino Acid Transport System y+, Ubiquinone, Iron, Oxidants, Phospholipid Hydroperoxide Glutathione Peroxidase, Glutathione, Mitochondria, Small Molecule Libraries, Gene Expression Regulation, Perspective, Ferroptosis, Humans, S100 Calcium-Binding Protein A4, Lipid Peroxidation, GTP Cyclohydrolase, Reactive Oxygen Species, Cells, Cultured, Signal Transduction
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