Kong Yuanyuan, Li Jing, Lin Rufeng, Lu Shifeng, Rong Liucheng, Xue Yao, Fang Yongjun
Department of Hematology and Oncology, Children's Hospital of Nanjing Medical University, Nanjing, China.
Department of Clinical Laboratory, Maternal and Child Health Care of Zaozhuang, Zaozhuang, China.
Front Cell Dev Biol. 2024 Mar 18;11:1329147. doi: 10.3389/fcell.2023.1329147. eCollection 2023.
Ferroptosis is an iron-dependent form of regulated cell death and is characterized by high concentrations of intracellular lipid peroxide and a redox imbalance in the cells. Ferroptosis shows distinct morphological and biological features compared with other prominent mechanisms of programmed cell death. The distinct characteristics of ferroptosis include the dysfunction of the lipid peroxide repair enzyme glutathione peroxidase 4, the presence of ferrous iron overload, and the lipid peroxidation of polyunsaturated fatty acids. Several other metabolic pathways (including iron, lipid, and amino acid metabolism) and ferritinophagy, as well as transcription factors, can modulate ferroptosis. However, to date, the molecular mechanism of ferroptosis has not been elucidated. This review outlines the discovery, characterization, regulatory mechanisms, and crosstalk of ferroptosis. Further, we have noted the controversial elements in the ferroptosis-related mechanisms. Our inferences may provide a partial reference for developing strategies to regulate ferroptosis.
铁死亡是一种铁依赖性的程序性细胞死亡形式,其特征是细胞内脂质过氧化物浓度高且细胞内存在氧化还原失衡。与其他突出的程序性细胞死亡机制相比,铁死亡具有独特的形态学和生物学特征。铁死亡的独特特征包括脂质过氧化物修复酶谷胱甘肽过氧化物酶4功能失调、亚铁过载以及多不饱和脂肪酸的脂质过氧化。其他几种代谢途径(包括铁、脂质和氨基酸代谢)以及铁自噬,还有转录因子,均可调节铁死亡。然而,迄今为止,铁死亡的分子机制尚未阐明。本综述概述了铁死亡的发现、特征、调控机制及相互作用。此外,我们还指出了铁死亡相关机制中存在争议的部分。我们的推断可能为制定调节铁死亡的策略提供部分参考。