Lipid storage and lipophagy regulates ferroptosis

Biochem Biophys Res Commun. 2019 Jan 22;508(4):997-1003. doi: 10.1016/j.bbrc.2018.12.039. Epub 2018 Dec 11.

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.

Keywords: Autophagy; Ferroptosis; Lipid degradation; Lipid droplets; Lipid storage.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Autophagy* / drug effects
  • Autophagy-Related Protein 5 / metabolism
  • Carbolines / pharmacology
  • Hep G2 Cells
  • Humans
  • Iron / metabolism
  • Lipid Droplets / drug effects
  • Lipid Droplets / metabolism
  • Lipid Metabolism* / drug effects
  • Mice
  • Neoplasm Proteins / metabolism
  • rab GTP-Binding Proteins / metabolism
  • rab7 GTP-Binding Proteins

Substances

  • Autophagy-Related Protein 5
  • Carbolines
  • Neoplasm Proteins
  • RSL3 compound
  • Tpd52 protein, mouse
  • rab7 GTP-Binding Proteins
  • Iron
  • rab GTP-Binding Proteins