细胞器
神经退行性变
高尔基体
内质网
细胞生物学
线粒体
程序性细胞死亡
过氧化物酶体
生物
细胞凋亡
疾病
病理
医学
生物化学
基因
作者
Xin Chen,Rui Kang,Guido Kroemer,Daolin Tang
标识
DOI:10.1038/s41418-021-00859-z
摘要
Ferroptosis, a cell death modality characterized by iron-dependent lipid peroxidation, is involved in the development of multiple pathological conditions, including ischemic tissue damage, infection, neurodegeneration, and cancer. The cellular machinery responsible for the execution of ferroptosis integrates multiple pro-survival or pro-death signals from subcellular organelles and then 'decides' whether to engage the lethal process or not. Here, we outline the evidence implicating different organelles (including mitochondria, lysosomes, endoplasmic reticulum, lipid droplets, peroxisomes, Golgi apparatus, and nucleus) in the ignition or avoidance of ferroptosis, while emphasizing their potential relevance for human disease and their targetability for pharmacological interventions.
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