GPX4
细胞生物学
程序性细胞死亡
线粒体
脂质过氧化
细胞质
机制(生物学)
生物
化学
氧化应激
细胞凋亡
生物化学
超氧化物歧化酶
哲学
认识论
谷胱甘肽过氧化物酶
作者
Tianliang Ma,Jing-Xian Chen,Peng Zhu,Chao-Bin Zhang,Yong Zhou,Jia‐Xi Duan
出处
期刊:Life Sciences
[Elsevier]
日期:2022-08-06
卷期号:307: 120868-120868
被引量:44
标识
DOI:10.1016/j.lfs.2022.120868
摘要
Ferroptosis is a kind of iron-dependent regulatory necrosis characterized by the fatal accumulation of iron-dependent lipid peroxides in the plasma membrane and the final oxidative damage of the cell membrane. Morphologically, ferroptosis features high membrane density, decreased or disappeared cristae, rupture of the mitochondrial outer membrane, plasma membrane integrity loss, cytoplasmic swelling, and organelle swelling. Under physiological conditions, ferroptosis occurs through two major pathways, the extrinsic or transporter-dependent pathway and the intrinsic or enzyme-regulated pathway, triggered by a series of small molecules inside and outside the cell. At present, it is assumed that ferroptosis is mainly related to abnormal toxicity of iron, lipid peroxidation, and mitochondrial dysfunction. With more detailed studies, ferroptosis plays potential pathogenic roles in multisystem diseases as a pathological response, and targeted regulation of ferroptosis in treating ferroptosis-related diseases has broad prospects. In conclusion, it is of great clinical significance to further clarify the specific mechanism of ferroptosis and explore new strategies for ferroptosis regulation. The present review emphatically summarizes the latest mechanism of ferroptosis, focusing on the regulation mechanism and clinical application of ferroptosis inducers and inhibitors. We are devoted to providing new ideas for the further study of ferroptosis and the diagnosis and treatment of ferroptosis-related multisystem diseases.
科研通智能强力驱动
Strongly Powered by AbleSci AI