Department of Biological Sciences, Columbia University, New York, New York, United States of America.
Department of Chemistry, Columbia University, New York, New York, United States of America.
PLoS Biol. 2018 May 24;16(5):e2006203. doi: 10.1371/journal.pbio.2006203. eCollection 2018 May.
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.
铁死亡是一种由细胞膜损伤驱动的细胞死亡过程,与许多人类疾病有关。铁死亡是由负责修复细胞膜氧化损伤的关键酶——谷胱甘肽过氧化物酶 4 (GPX4) 失活引起的。GPX4 通常会清除铁依赖性脂质过氧化的危险产物,从而保护细胞膜免受这种损伤;当 GPX4 失效时,铁死亡就会发生。铁死亡与细胞凋亡、坏死、细胞坏死和其他细胞死亡方式不同。关于细胞在铁死亡过程中如何死亡的几个关键谜团仍未解开。首先,脂质过氧化的驱动因素尚不清楚。其次,致命脂质过氧化物的亚细胞位置仍然是一个悬而未决的问题。最后,脂质过氧化如何导致细胞死亡仍然是一个未解之谜。这些问题的答案将为铁死亡细胞死亡的机制和相关人类疾病提供深入的了解,并为这些疾病提供新的治疗策略。