GPX4
脂质过氧化
坏死性下垂
程序性细胞死亡
磷脂过氧化氢谷胱甘肽过氧化物酶
生物
细胞生物学
细胞凋亡
氧化应激
细胞
生物化学
谷胱甘肽过氧化物酶
过氧化氢酶
作者
Huizhong Feng,Brent R. Stockwell
出处
期刊:PLOS Biology
[Public Library of Science]
日期:2018-05-24
卷期号:16 (5): e2006203-e2006203
被引量:512
标识
DOI:10.1371/journal.pbio.2006203
摘要
Ferroptosis is a cell death process driven by damage to cell membranes and linked to numerous human diseases. Ferroptosis is caused by loss of activity of the key enzyme that is tasked with repairing oxidative damage to cell membranes-glutathione peroxidase 4 (GPX4). GPX4 normally removes the dangerous products of iron-dependent lipid peroxidation, protecting cell membranes from this type of damage; when GPX4 fails, ferroptosis ensues. Ferroptosis is distinct from apoptosis, necroptosis, necrosis, and other modes of cell death. Several key mysteries regarding how cells die during ferroptosis remain unsolved. First, the drivers of lipid peroxidation are not yet clear. Second, the subcellular location of lethal lipid peroxides remains an outstanding question. Finally, how exactly lipid peroxidation leads to cell death is an unsolved mystery. Answers to these questions will provide insights into the mechanisms of ferroptotic cell death and associated human diseases, as well as new therapeutic strategies for such diseases.
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