The G protein-coupled receptor G2A: involvement in hepatic lipid metabolism and gallstone formation in mice

Hepatology. 2008 Oct;48(4):1138-48. doi: 10.1002/hep.22433.

Abstract

The G2A receptor is a member of the ovarian cancer G protein-coupled receptor 1 family of stress-inducible G protein-coupled receptors. In this study, we examined the hepatobiliary effects of loss of function of G2A in mice fed either a chow or lithogenic diet. G2A-deficient (G2A(-/-)) mice fed chow had a 25% reduction in biliary phosphatidylcholine content, reduced hepatic gene expression of the phosphatidylcholine transporter adenosine triphosphate-binding cassette B4, and an 8-fold increase in expression of the nuclear receptor liver X receptor (LXR). Despite the increased expression of LXR, transcription of several LXR target genes was reduced. G2A(-/-) mice fed a lithogenic diet had rapid gallstone formation, an increased cholesterol saturation index, a 2.5-fold increase in farnesoid X receptor expression, a 5-fold increase in LXR expression, and a 90% reduction in cholesterol 7alpha-hydroxylase expression in comparison with wild-type mice. There were no changes in gallbladder volume.

Conclusion: These data demonstrate that the G2A receptor is important for hepatobiliary bile salt, cholesterol, and phospholipid homeostasis and for the pathogenesis of cholesterol gallstone formation.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Bile Acids and Salts / metabolism
  • Cell Cycle Proteins / genetics
  • Cell Cycle Proteins / metabolism*
  • Cholesterol / metabolism
  • DNA-Binding Proteins / metabolism
  • Diet / adverse effects
  • Disease Models, Animal
  • Female
  • Gallstones / chemically induced
  • Gallstones / genetics
  • Gallstones / metabolism*
  • Homeostasis / physiology
  • Lipid Metabolism / genetics
  • Lipid Metabolism / physiology*
  • Liver / metabolism*
  • Liver X Receptors
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Orphan Nuclear Receptors
  • Phospholipids / metabolism
  • Receptors, Cytoplasmic and Nuclear / metabolism
  • Receptors, G-Protein-Coupled / genetics
  • Receptors, G-Protein-Coupled / metabolism*
  • Transcription Factors / metabolism

Substances

  • Bile Acids and Salts
  • Cell Cycle Proteins
  • DNA-Binding Proteins
  • G2A receptor
  • Liver X Receptors
  • Orphan Nuclear Receptors
  • Phospholipids
  • Receptors, Cytoplasmic and Nuclear
  • Receptors, G-Protein-Coupled
  • Transcription Factors
  • farnesoid X-activated receptor
  • Cholesterol