脂质过氧化
活性氧
生物化学
过氧化氢
生物
GPX4
抗氧化剂
细胞色素b5
还原酶
多不饱和脂肪酸
氧化还原酶
NAD+激酶
膜脂
磷脂过氧化氢谷胱甘肽过氧化物酶
细胞生物学
膜
酶
脂肪酸
过氧化氢酶
谷胱甘肽过氧化物酶
作者
Bo Yan,Youwei Ai,Qi Sun,Yan Ma,Yang Cao,Jiawen Wang,Zhiyuan Zhang,Xiaodong Wang
出处
期刊:Molecular Cell
[Elsevier BV]
日期:2020-12-15
卷期号:81 (2): 355-369.e10
被引量:481
标识
DOI:10.1016/j.molcel.2020.11.024
摘要
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.
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