脂滴
脂质过氧化
程序性细胞死亡
脂质代谢
自噬
细胞生物学
ATG5型
细胞内
化学
细胞
生物
GPX4
细胞凋亡
生物化学
谷胱甘肽
抗氧化剂
酶
谷胱甘肽过氧化物酶
作者
Yuansong Bai,Lingjun Meng,Leng Han,Yuanyuan Jia,Xinwei Han,Huan Gao,Rui Kang,Xiaofeng Wang,Daolin Tang,Enyong Dai
标识
DOI:10.1016/j.bbrc.2018.12.039
摘要
The synthesis, storage, and degradation of lipids are highly regulated processes. Impaired lipid metabolism is implicated in inflammation and cell death. Although ferroptosis is a recently described form of regulated cell death driven by lipid peroxidation, the impact of lipid droplets on ferroptosis remains unidentified. Here, we demonstrate that lipophagy, the autophagic degradation of intracellular lipid droplets, promotes RSL3-induced ferroptotic cell death in hepatocytes. Lipid droplet accumulation is increased at the early stage but decreased at the late stage of ferroptosis in mouse or human hepatocytes. Importantly, either genetically enhancing TPD52-dependent lipid storage or blocking ATG5-and RAB7A-dependent lipid degradation prevents RSL3-induced lipid peroxidation and subsequent ferroptosis in vitro and in vivo. These studies support an antioxidant role for lipid droplets in cell death and suggest novel strategies for the inhibition of ferroptosis by targeting the lipophagy pathway.
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