Hepatocyte growth factor up-regulates met expression in rat fetal hepatocytes in primary culture

Biochem Biophys Res Commun. 1994 Nov 15;204(3):1364-70. doi: 10.1006/bbrc.1994.2614.

Abstract

Hepatocyte growth factor (HGF) is a potent mitogen for primary cultured fetal hepatocytes. In the present study, we have analyzed the c-met/HGF receptor expression in fetal hepatocytes and its modulation by growth factors and hormones. 20-day old fetal liver showed a barely expression of c-met mRNA levels. However, when fetal hepatocytes were incubated in the presence of HGF, a 10-fold increase in c-met mRNA levels was observed 30 min after addition of the factor. This HGF-induced effect on c-met expression was transient, losing its up-regulatory effect after 24 hours and returning to the initial levels at 48 hours. Transforming growth factor-beta, a negative regulator of fetal liver growth, increased c-met mRNA levels 48 hours after the addition of the factor, whereas glucocorticoids had a negative effect.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blotting, Northern
  • Cells, Cultured
  • Dexamethasone / pharmacology
  • Fetus
  • Fibronectins / biosynthesis
  • Gene Expression / drug effects*
  • Gestational Age
  • Hepatocyte Growth Factor / pharmacology*
  • Humans
  • Liver / cytology
  • Liver / drug effects
  • Liver / metabolism*
  • Proto-Oncogene Proteins / biosynthesis
  • Proto-Oncogene Proteins c-met
  • Proto-Oncogenes / drug effects
  • RNA, Messenger / analysis
  • RNA, Messenger / biosynthesis
  • Rats
  • Rats, Wistar
  • Receptor Protein-Tyrosine Kinases / biosynthesis*
  • Recombinant Proteins / pharmacology
  • Serum Albumin / biosynthesis
  • Up-Regulation
  • alpha-Fetoproteins / biosynthesis

Substances

  • Fibronectins
  • Proto-Oncogene Proteins
  • RNA, Messenger
  • Recombinant Proteins
  • Serum Albumin
  • alpha-Fetoproteins
  • Hepatocyte Growth Factor
  • Dexamethasone
  • Proto-Oncogene Proteins c-met
  • Receptor Protein-Tyrosine Kinases