生物
自噬
程序性细胞死亡
背景(考古学)
细胞生物学
双重角色
生物化学
化学
细胞凋亡
古生物学
组合化学
作者
Xin Chen,Andrey S. Tsvetkov,Han‐Ming Shen,Ciro Isidoro,Nicholas T. Ktistakis,Andreas Linkermann,Werner J.H. Koopman,Hans‐Uwe Simon,Lorenzo Galluzzi,Shouqing Luo,Daqian Xu,Wei Gu,Olivier Peulen,Qian Cai,David C. Rubinsztein,Jen‐Tsan Chi,Donna D. Zhang,Changfeng Li,Shinya Toyokuni,Jinbao Liu
出处
期刊:Autophagy
[Taylor & Francis]
日期:2024-03-06
卷期号:20 (6): 1213-1246
被引量:64
标识
DOI:10.1080/15548627.2024.2319901
摘要
Macroautophagy/autophagy is a complex degradation process with a dual role in cell death that is influenced by the cell types that are involved and the stressors they are exposed to. Ferroptosis is an iron-dependent oxidative form of cell death characterized by unrestricted lipid peroxidation in the context of heterogeneous and plastic mechanisms. Recent studies have shed light on the involvement of specific types of autophagy (e.g. ferritinophagy, lipophagy, and clockophagy) in initiating or executing ferroptotic cell death through the selective degradation of anti-injury proteins or organelles. Conversely, other forms of selective autophagy (e.g. reticulophagy and lysophagy) enhance the cellular defense against ferroptotic damage. Dysregulated autophagy-dependent ferroptosis has implications for a diverse range of pathological conditions. This review aims to present an updated definition of autophagy-dependent ferroptosis, discuss influential substrates and receptors, outline experimental methods, and propose guidelines for interpreting the results.
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