Lipid storage and lipophagy regulates ferroptosis

被引:368
作者
Bai, Yuansong [1 ]
Meng, Lingjun [1 ]
Han, Leng [1 ]
Jia, Yuanyuan [1 ]
Zhao, Yanan [1 ]
Gao, Huan [1 ]
Kang, Rui [2 ]
Wang, Xiaofeng [3 ]
Tang, Daolin [2 ]
Dai, Enyong [1 ]
机构
[1] Jilin Univ, China Japan Union Hosp, Dept Oncol & Hematol, Changchun 130033, Jilin, Peoples R China
[2] UT Southwestern Med Ctr, Dept Surg, Dallas, TX 75390 USA
[3] Jilin Univ, China Japan Union Hosp, Dept Stomatol, Changchun 130033, Jilin, Peoples R China
基金
美国国家卫生研究院; 中国国家自然科学基金;
关键词
Ferroptosis; Autophagy; Lipid droplets; Lipid storage; Lipid degradation; CELL-DEATH RECOMMENDATIONS; AUTOPHAGY; METABOLISM; STARVATION; BIOLOGY; IDENTIFICATION; DEGRADATION; MECHANISMS; DROPLETS; AUTOSIS;
D O I
10.1016/j.bbrc.2018.12.039
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
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. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:997 / 1003
页数:7
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