Journal Article

Oxidized arachidonic and adrenic PEs navigate cells to ferroptosis

Bayır, Hülya, Ritov, Vladimir B, Klein-Seetharaman, Judith, Yang, Qin, Amoscato, Andrew A, Greenberger, Joel, Tyurina, Yulia Y, Mao, Gaowei, Liu, Bing, Mallampalli, Rama K, Tyurin, Vladimir A, Bahar, Ivet, Qu, Feng, Anthonymuthu, Tamil, Stockwell, Brent R, Doll, Sebastian, Kapralov, Alexandr A, Jiang, Jianfei, Proneth, Bettina, Conrad, Marcus, Watkins, Simon, Kagan, Valerian E, Mohammadyani, Dariush, Angeli, Jose Pedro Friedmann, Dar, Haider Hussain, Croix, Claudette St

2017

Overview

Arachidonyl and adrenoyl PE phospholipids generated by ACSL4, an acyl-CoA synthase, are doubly or triply oxidized by lipoxygenases and other iron-containing sources of oxidation to promote ferroptotic cell death. Enigmatic lipid peroxidation products have been claimed as the proximate executioners of ferroptosis—a specialized death program triggered by insufficiency of glutathione peroxidase 4 (GPX4). Using quantitative redox lipidomics, reverse genetics, bioinformatics and systems biology, we discovered that ferroptosis involves a highly organized oxygenation center, wherein oxidation in endoplasmic-reticulum-associated compartments occurs on only one class of phospholipids (phosphatidylethanolamines (PEs)) and is specific toward two fatty acyls—arachidonoyl (AA) and adrenoyl (AdA). Suppression of AA or AdA esterification into PE by genetic or pharmacological inhibition of acyl-CoA synthase 4 (ACSL4) acts as a specific antiferroptotic rescue pathway. Lipoxygenase (LOX) generates doubly and triply-oxygenated (15-hydroperoxy)-diacylated PE species, which act as death signals, and tocopherols and tocotrienols (vitamin E) suppress LOX and protect against ferroptosis, suggesting a homeostatic physiological role for vitamin E. This oxidative PE death pathway may also represent a target for drug discovery.

• Publisher: Nature Publishing Group US,Nature Publishing Group
• Subject: 631/114 / 631/45/608 / 631/553 / 631/80/82 / Animals / Arachidonic Acid - antagonists & inhibitors / Arachidonic Acid - metabolism / Biochemical Engineering / Biochemistry / Bioinformatics / Bioorganic Chemistry / Cell Biology / Cell Death - drug effects / Cell Line / Chemistry / Chemistry/Food Science / Coenzyme A Ligases - antagonists & inhibitors / Coenzyme A Ligases - deficiency / Coenzyme A Ligases - metabolism / Fatty Acids, Unsaturated - antagonists & inhibitors / Fatty Acids, Unsaturated - metabolism / Female / Ferroptosis / Genetics / Male / Mice / Mice, Inbred C57BL / Mice, Knockout / Mortality / Oxygenation / Peroxidation / Phospholipids - metabolism