A novel HIF2A mutation causes dyslipidemia and promotes hepatic lipid accumulation

Pharmacol Res. 2023 Aug:194:106851. doi: 10.1016/j.phrs.2023.106851. Epub 2023 Jul 13.

Abstract

Hypoxia-inducible factor-2α (HIF-2α) is a transcription factor responsible for regulating genes related to angiogenesis and metabolism. This study aims to explore the effect of a previously unreported mutation c.C2473T (p.R825S) in the C-terminal transactivation domain (CTAD) of HIF-2α that we detected in tissue of patients with liver disease. We sequenced available liver and matched blood samples obtained during partial liver resection or liver transplantation performed for clinical indications including hepatocellular carcinoma and liver failure. In tandem, we constructed cell lines and a transgenic mouse model bearing the corresponding identified mutation in HIF-2α from which we extracted primary hepatocytes. Lipid accumulation was evaluated in these cells and liver tissue from the mouse model using Oil Red O staining and biochemical measurements. We identified a mutation in the CTAD of HIF-2α (c.C2473T; p.R825S) in 5 of 356 liver samples obtained from patients with hepatopathy and dyslipidemia. We found that introduction of this mutation into the mouse model led to an elevated triglyceride level, lipid droplet accumulation in liver of the mutant mice and in their extracted primary hepatocytes, and increased transcription of genes related to hepatic fatty acid transport and synthesis in the mutant compared to the control groups. In mutant mice and cells, the protein levels of nuclear HIF-2α and its target perilipin-2 (PLIN2), a lipid droplet-related gene, were also elevated. Decreased lipophagy was observed in mutant groups. Our study defines a subpopulation of dyslipidemia that is caused by this HIF-2α mutation. This may have implications for personalized treatment.

Keywords: Cholesterol (PubChem CID: 5997); Dexamethasone (PubChem CID: 5743); Hypoxia-inducible factor-2α; Lipid droplet; Lipophagy; Methanol (PubChem CID: 887); Mutation; Non-alcoholic fatty liver; Oleic Acid (PubChem CID: 445639); Palmitic Acid (PubChem CID: 985); Perilipin-2; Puromycin (PubChem CID: 439530); Streptomycin (PubChem CID: 19649).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Basic Helix-Loop-Helix Transcription Factors / genetics
  • Basic Helix-Loop-Helix Transcription Factors / metabolism
  • Dyslipidemias* / genetics
  • Humans
  • Lipids
  • Liver Neoplasms*
  • Mice
  • Mutation

Substances

  • Basic Helix-Loop-Helix Transcription Factors
  • endothelial PAS domain-containing protein 1
  • Lipids