Increased expression of mRNA for hepatocyte growth factor-like protein during liver regeneration and inflammation

Biochem Biophys Res Commun. 1994 Aug 30;203(1):666-73. doi: 10.1006/bbrc.1994.2234.

Abstract

To assess potential roles of hepatocyte growth factor-like (HGFL) protein as a growth factor and as a cytokine, we determined the expression of mRNA for (HGFL) protein during liver regeneration and inflammation. Expression of mRNA for HGFL protein in the regenerating liver was upregulated to 93% and 64% above controls at 1 h following partial hepatectomy and carbon tetrachloride treatment of rats, respectively. Similarly, rat liver mRNA for HGFL protein was upregulated to 78% above controls at 24 h after injection of thioglycollate (inducing activation of peritoneal macrophages) and to 118% at 48 h after injection of turpentine (inducing the acute phase response). These results support a potential role for HGFL protein in the early phase of liver regeneration and as an inflammatory mediator.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Carbon Tetrachloride / toxicity
  • Gene Expression*
  • Growth Substances / biosynthesis*
  • Hepatectomy
  • Hepatocyte Growth Factor*
  • In Situ Hybridization
  • Inflammation / chemically induced
  • Inflammation / metabolism*
  • Kinetics
  • Liver / drug effects
  • Liver / metabolism*
  • Liver / pathology
  • Liver Regeneration*
  • Male
  • Oligonucleotide Probes
  • Plasmids
  • Proto-Oncogene Proteins*
  • RNA, Messenger / biosynthesis
  • Rats
  • Rats, Sprague-Dawley
  • Thioglycolates / toxicity
  • Time Factors
  • Turpentine / toxicity

Substances

  • Growth Substances
  • Oligonucleotide Probes
  • Proto-Oncogene Proteins
  • RNA, Messenger
  • Thioglycolates
  • macrophage stimulating protein
  • Hepatocyte Growth Factor
  • Carbon Tetrachloride
  • Turpentine