| Literature DB >> 30545638 |
Yuansong Bai1, Lingjun Meng1, Leng Han1, Yuanyuan Jia1, Yanan Zhao1, Huan Gao1, Rui Kang2, Xiaofeng Wang3, Daolin Tang4, Enyong Dai5.
Abstract
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.Entities:
Keywords: Autophagy; Ferroptosis; Lipid degradation; Lipid droplets; Lipid storage
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Year: 2018 PMID: 30545638 DOI: 10.1016/j.bbrc.2018.12.039
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575