GPX4
线粒体
诱导剂
细胞凋亡
脂质过氧化
化学
去铁胺
癌细胞
细胞
生物化学
线粒体内膜
程序性细胞死亡
细胞生物学
生物
氧化应激
癌症
基因
遗传学
谷胱甘肽过氧化物酶
过氧化氢酶
作者
Hua Yuan,Xuemei Li,Xiuying Zhang,Rui Kang,Daolin Tang
标识
DOI:10.1016/j.bbrc.2016.08.034
摘要
Ferroptosis is a form of non-apoptotic cell death originally identified in cancer cells. However, the key regulator of ferroptosis in mitochondria remains unknown. Here, we show that CDGSH iron sulfur domain 1 (CISD1, also termed mitoNEET), an iron-containing outer mitochondrial membrane protein, negatively regulates ferroptotic cancer cell death. The classical ferroptosis inducer erastin promotes CISD1 expression in an iron-dependent manner in human hepatocellular carcinoma cells (e.g., HepG2 and Hep3B). Genetic inhibition of CISD1 increased iron-mediated intramitochondrial lipid peroxidation, which contributes to erastin-induced ferroptosis. In contrast, stabilization of the iron sulfur cluster of CISD1 by pioglitazone inhibits mitochondrial iron uptake, lipid peroxidation, and subsequent ferroptosis. These findings indicate a novel role of CISD1 in protecting against mitochondrial injury in ferroptosis.
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