Estrogen-related receptor γ regulates hepatic triglyceride metabolism through phospholipase A2 G12B

FASEB J. 2019 Jul;33(7):7942-7952. doi: 10.1096/fj.201802704R. Epub 2019 Mar 28.

Abstract

Hypersecretion of hepatic very LDL (VLDL)-associated triglyceride (TG) is the hallmark of hypertriglyceridemia. The estrogen-related receptor γ (ERRγ), an orphan nuclear receptor, plays crucial roles in the regulation of metabolic homeostasis, including TG formation in the liver. It remains unclear whether ERRγ regulates hepatic VLDL-TG secretion. We demonstrated that knockdown of ERRγ impairs hepatic VLDL-TG secretion in mice, whereas overexpression of ERRγ favors the secretion, indicating a novel role of ERRγ in hepatic TG metabolism. We found that ERRγ transcriptionally regulates the expression of PLA2G12B by binding to the promoter region of the Pla2g12b gene. In Pla2g12b-null mice, ERRγ fails to regulate hepatic VLDL-TG secretion. There is an apparent accumulation of large lipid droplets in the liver of Pla2g12b-null mice. These data suggest that ERRγ is a novel regulator of hepatic VLDL-TG secretion, which is mediated through the action on PLA2G12B.-Chen, L., Wu, M., Zhang, S., Tan, W., Guan, M., Feng, L., Chen, C., Tao, J., Chen, L., Qu, L. Estrogen-related receptor γ regulates hepatic triglyceride metabolism through phospholipase A2 G12B.

Keywords: ERRγ; PLA2G12B; VLDL secretion; hypertriglyceridemia.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Cholesterol / blood
  • Gene Knockdown Techniques
  • Group X Phospholipases A2 / deficiency
  • Group X Phospholipases A2 / genetics
  • Group X Phospholipases A2 / physiology*
  • Lipoproteins, VLDL / metabolism*
  • Liver / metabolism*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Promoter Regions, Genetic
  • RNA Interference
  • RNA, Small Interfering / genetics
  • RNA, Small Interfering / pharmacology
  • Receptors, Estrogen / genetics
  • Receptors, Estrogen / physiology*
  • Recombinant Proteins / metabolism
  • Transcription, Genetic
  • Triglycerides / blood
  • Triglycerides / metabolism*
  • Up-Regulation

Substances

  • ESRRG protein, human
  • Esrrg protein, mouse
  • Lipoproteins, VLDL
  • RNA, Small Interfering
  • Receptors, Estrogen
  • Recombinant Proteins
  • Triglycerides
  • very low density lipoprotein triglyceride
  • Cholesterol
  • Group X Phospholipases A2
  • PLA2G12B protein, mouse