Yang Wan Seok, Stockwell Brent R
Department of Biological Sciences, Howard Hughes Medical Institute, Columbia University, New York, NY, USA.
Department of Biological Sciences, Howard Hughes Medical Institute, Columbia University, New York, NY, USA; Department of Chemistry, Columbia University, New York, NY, USA; Department of Systems Biology, Columbia University, New York, NY, USA.
Trends Cell Biol. 2016 Mar;26(3):165-176. doi: 10.1016/j.tcb.2015.10.014. Epub 2015 Dec 2.
Ferroptosis is a regulated form of cell death driven by loss of activity of the lipid repair enzyme glutathione peroxidase 4 (GPX4) and subsequent accumulation of lipid-based reactive oxygen species (ROS), particularly lipid hydroperoxides. This form of iron-dependent cell death is genetically, biochemically, and morphologically distinct from other cell death modalities, including apoptosis, unregulated necrosis, and necroptosis. Ferroptosis is regulated by specific pathways and is involved in diverse biological contexts. Here we summarize the discovery of ferroptosis, the mechanism of ferroptosis regulation, and its increasingly appreciated relevance to both normal and pathological physiology.
铁死亡是一种由脂质修复酶谷胱甘肽过氧化物酶4(GPX4)活性丧失以及随后基于脂质的活性氧(ROS)尤其是脂质氢过氧化物积累所驱动的程序性细胞死亡形式。这种铁依赖性细胞死亡在遗传、生化和形态学上与其他细胞死亡方式不同,包括凋亡、非程序性坏死和坏死性凋亡。铁死亡由特定途径调控,并参与多种生物学过程。在这里,我们总结了铁死亡的发现、铁死亡调控机制及其在正常和病理生理学中日益受到重视的相关性。
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