GPX4
脂质过氧化
脂质代谢
机制(生物学)
谷胱甘肽
新陈代谢
化学
生物化学
抗氧化剂
程序性细胞死亡
活性氧
谷胱甘肽过氧化物酶
细胞生物学
酶
生物
细胞凋亡
哲学
认识论
作者
Xu-Dong Zhang,Zhongyuan Liu,Mao-Sen Wang,Y. Guo,Xiangkun Wang,Kai Luo,Shuai Huang,Renfeng Li
标识
DOI:10.3389/fimmu.2023.1269451
摘要
Regulation of cell mortality for disease treatment has been the focus of research. Ferroptosis is an iron-dependent regulated cell death whose mechanism has been extensively studied since its discovery. A large number of studies have shown that regulation of ferroptosis brings new strategies for the treatment of various benign and malignant diseases. Iron excess and lipid peroxidation are its primary metabolic features. Therefore, genes involved in iron metabolism and lipid metabolism can regulate iron overload and lipid peroxidation through direct or indirect pathways, thereby regulating ferroptosis. In addition, glutathione (GSH) is the body's primary non-enzymatic antioxidants and plays a pivotal role in the struggle against lipid peroxidation. GSH functions as an auxiliary substance for glutathione peroxidase 4 (GPX4) to convert toxic lipid peroxides to their corresponding alcohols. Here, we reviewed the researches on the mechanism of ferroptosis in recent years, and comprehensively analyzed the mechanism and regulatory process of ferroptosis from iron metabolism and lipid metabolism, and then described in detail the metabolism of GPX4 and the main non-enzymatic antioxidant GSH in vivo.
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