脂质过氧化
脂类学
细胞生物学
GPX4
膜脂
细胞器
脂质代谢
化学
脂滴
脂质双层
内质网
氧化磷酸化
多不饱和脂肪酸
脂质微区
生物物理学
脂筏
脂质信号
磷脂
生物
线粒体
抗氧化剂
新陈代谢
过氧亚硝酸盐
脂质体
膜蛋白
脂毒性
细胞膜
生物化学
氧化应激
作者
Mike Lange,Michele Wölk,Vivian Li,Cody E. Doubravsky,Joseph M. Hendricks,Shunji Kato,Yurika Otoki,Benjamin S. Styler,Sean L. Johnson,Carolyn Harris,Kiyotaka Nakagawa,Isabel F. Snodgrass,Do‐Hee Kim,John W. Newman,Maria Fedorova,James A. Olzmann
标识
DOI:10.1038/s41556-025-01790-y
摘要
Abstract Lipid droplets (LDs) are organelles that store and supply lipids, based on cellular needs. Although mechanisms preventing oxidative damage to membrane phospholipids are established, the vulnerability of LD neutral lipids to peroxidation and protective mechanisms are unknown. Here we identify LD-localized ferroptosis suppressor protein 1 (FSP1) as a critical regulator that prevents neutral lipid peroxidation by recycling coenzyme Q10 (CoQ10) to its lipophilic antioxidant form. Lipidomics reveal that FSP1 loss leads to the accumulation of oxidized triacylglycerols and cholesteryl esters, and biochemical reconstitution of FSP1 with CoQ10 and NADH suppresses triacylglycerol peroxidation in vitro. Notably, inducing polyunsaturated fatty acid-rich LDs triggers triacylglycerol peroxidation and LD-initiated ferroptosis when FSP1 activity is impaired. These findings uncover the first LD lipid quality-control pathway, wherein LD-localized FSP1 maintains neutral lipid integrity to prevent the build-up of oxidized lipids and induction of ferroptosis.
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