Relaxin receptor expression in hepatic stellate cells and in cirrhotic rat liver tissue

Robert G. Bennett, Katrina J. Mahan, Martha J. Gentry-Nielsen, Dean J. Tuma

Research output: Contribution to journalArticle

11 Scopus citations

Abstract

Relaxin has antifibrotic effects on the hepatic stellate cells (HSCs) responsible for collagen deposition in cirrhosis. The expression of relaxin receptors LGR7 and LGR8 in HSCs and liver disease was examined. Activated and quiescent HSCs expressed LGR7, whereas only activated HSCs expressed LGR8. Relaxin, relaxin-3, or InsL3 treatment increased cAMP, suggesting activation of both receptors. LGR8 and LGR7 were present in cirrhotic rat liver, but were undetectable in normal liver. In conclusion, both LGR7 and LGRS are expressed in activated HSCs and cirrhotic liver, suggesting that relaxin, InsL3, or relaxin-3 may be useful in the treatment of hepatic fibrosis.

Original languageEnglish (US)
Pages (from-to)185-189
Number of pages5
JournalAnnals of the New York Academy of Sciences
Volume1041
DOIs
StatePublished - Jan 1 2005

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Keywords

  • Hepatic fibrosis
  • Hepatic stellate cell
  • InsL3
  • LGR7
  • LGR8
  • Relaxin
  • Relaxin-3

ASJC Scopus subject areas

  • Neuroscience(all)
  • Biochemistry, Genetics and Molecular Biology(all)
  • History and Philosophy of Science

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