Membrane Damage during Ferroptosis Is Caused by Oxidation of Phospholipids Catalyzed by the Oxidoreductases POR and CYB5R1

Mol Cell. 2021 Jan 21;81(2):355-369.e10. doi: 10.1016/j.molcel.2020.11.024. Epub 2020 Dec 14.

Abstract

Ferroptosis is a form of necrotic cell death caused by iron-dependent peroxidation of polyunsaturated phospholipids on cell membranes and is actively suppressed by the cellular antioxidant systems. We report here that oxidoreductases, including NADPH-cytochrome P450 reductase (POR) and NADH-cytochrome b5 reductase (CYB5R1), transfer electrons from NAD(P)H to oxygen to generate hydrogen peroxide, which subsequently reacts with iron to generate reactive hydroxyl radicals for the peroxidation of the polyunsaturated fatty acid (PUFA) chains of membrane phospholipids, thereby disrupting membrane integrity during ferroptosis. Genetic knockout of POR and CYB5R1 decreases cellular hydrogen peroxide generation, preventing lipid peroxidation and ferroptosis. Moreover, POR knockdown in mouse liver prevents ConA-induced liver damage. Ferroptosis, therefore, is a result of incidental electron transfer carried out by POR/CYB5R1 oxidoreductase and thus needs to be constitutively countered by the antioxidant systems.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Cell Membrane / chemistry*
  • Cell Membrane / drug effects
  • Cell Membrane / metabolism
  • Concanavalin A / pharmacology
  • Cytochrome P-450 Enzyme System / deficiency
  • Cytochrome P-450 Enzyme System / genetics*
  • Cytochrome-B(5) Reductase / deficiency
  • Cytochrome-B(5) Reductase / genetics*
  • Electron Transport / drug effects
  • Fatty Acids, Unsaturated / metabolism*
  • Ferroptosis / drug effects
  • Ferroptosis / genetics*
  • HEK293 Cells
  • HeLa Cells
  • Humans
  • Hydrogen Peroxide / metabolism
  • Lipid Peroxidation / drug effects
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mice, Nude
  • NADP / metabolism*
  • Oxygen / metabolism
  • Phenylurea Compounds / pharmacology
  • Piperazines / pharmacology
  • Pyridines / pharmacology
  • Sorafenib / pharmacology

Substances

  • Fatty Acids, Unsaturated
  • POR protein, human
  • Phenylurea Compounds
  • Piperazines
  • Pyridines
  • erastin
  • Concanavalin A
  • regorafenib
  • NADP
  • Cytochrome P-450 Enzyme System
  • Sorafenib
  • Hydrogen Peroxide
  • CYB5R1 protein, human
  • Cytochrome-B(5) Reductase
  • Oxygen