FSP1-mediated lipid droplet quality control prevents neutral lipid peroxidation and ferroptosis

Publikation: Beitrag in FachzeitschriftForschungsartikelBeigetragenBegutachtung

Beitragende

  • Mike Lange - , University of California at Berkeley (Autor:in)
  • Michele Wölk - , Zentrum für Membranbiochemie und Lipidforschung (Autor:in)
  • Vivian Wen Li - , University of California at Berkeley (Autor:in)
  • Cody E Doubravsky - , University of California at Berkeley (Autor:in)
  • Joseph M Hendricks - , University of California at Berkeley (Autor:in)
  • Shunji Kato - , Tohoku University (Autor:in)
  • Yurika Otoki - , Tohoku University (Autor:in)
  • Benjamin Styler - , University of California at Berkeley (Autor:in)
  • Sean L Johnson - , University of California at Berkeley (Autor:in)
  • Cynthia A Harris - , University of California at Berkeley (Autor:in)
  • Kiyotaka Nakagawa - , Tohoku University (Autor:in)
  • Isabel F Snodgrass - , University of California at Davis (Autor:in)
  • Dohee Kim - , United States Department of Agriculture (Autor:in)
  • John W Newman - , University of California at Davis (Autor:in)
  • Maria Fedorova - , Zentrum für Membranbiochemie und Lipidforschung (Autor:in)
  • James A Olzmann - , University of California at Berkeley (Autor:in)

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.

Details

OriginalspracheEnglisch
Seiten (von - bis)1902-1913
Seitenumfang12
FachzeitschriftNature cell biology
Jahrgang27
Ausgabenummer11
PublikationsstatusVeröffentlicht - Nov. 2025
Peer-Review-StatusJa

Externe IDs

PubMedCentral PMC12611765
Scopus 105020079179
ORCID /0000-0002-4692-3885/work/200630951
ORCID /0000-0001-5558-4582/work/200631298

Schlagworte

Schlagwörter

  • Ferroptosis, Lipid Peroxidation, Humans, Lipid Droplets/metabolism, Animals, Triglycerides/metabolism, Ubiquinone/metabolism, Oxidation-Reduction, Mice, Lipidomics