Stomatin modulates adipogenesis through the ERK pathway and regulates fatty acid uptake and lipid droplet growth

Nat Commun. 2022 Jul 19;13(1):4174. doi: 10.1038/s41467-022-31825-z.

Abstract

Regulation of fatty acid uptake, lipid production and storage, and metabolism of lipid droplets (LDs), is closely related to lipid homeostasis, adipocyte hypertrophy and obesity. We report here that stomatin, a major constituent of lipid raft, participates in adipogenesis and adipocyte maturation by modulating related signaling pathways. In adipocyte-like cells, increased stomatin promotes LD growth or enlargements by facilitating LD-LD fusion. It also promotes fatty acid uptake from extracellular environment by recruiting effector molecules, such as FAT/CD36 translocase, to lipid rafts to promote internalization of fatty acids. Stomatin transgenic mice fed with high-fat diet exhibit obesity, insulin resistance and hepatic impairments; however, such phenotypes are not seen in transgenic animals fed with regular diet. Inhibitions of stomatin by gene knockdown or OB-1 inhibit adipogenic differentiation and LD growth through downregulation of PPARγ pathway. Effects of stomatin on PPARγ involves ERK signaling; however, an alternate pathway may also exist.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipogenesis* / genetics
  • Animals
  • CD36 Antigens / genetics
  • CD36 Antigens / metabolism
  • Diet, High-Fat
  • Fatty Acids / metabolism
  • Lipid Droplets* / metabolism
  • Lipid Metabolism
  • MAP Kinase Signaling System
  • Mice
  • Obesity / genetics
  • Obesity / metabolism
  • PPAR gamma / genetics
  • PPAR gamma / metabolism

Substances

  • CD36 Antigens
  • Fatty Acids
  • PPAR gamma