Distribution and isoforms of epimorphin in carbon tetrachloride-induced acute liver injury in mice

J Gastroenterol Hepatol. 2005 Nov;20(11):1769-80. doi: 10.1111/j.1440-1746.2005.03944.x.

Abstract

Background and aim: Epimorphin, a morphoregulatory factor essential to organ development, is believed to direct normal morphogenesis in tissue repair. We examined the dynamics and the roles of epimorphin, a cell surface-associated molecule detected on mesenchymal cells, in hepatic tissue repair from acute liver injury.

Methods: After acute liver injury was induced by carbon tetrachloride in Balb/c mice, the distribution of epimorphin-expressing cells was studied immunohistochemically. To clarify interactions between epimorphin expression and hepatocyte behavior, epimorphin-expressing cells and proliferating hepatocytes were counted. Then, epimorphin quantity and isoforms were assessed by western blotting. To better understand effects of epimorphin, we cultured rat hepatocytes in its presence.

Results: Epimorphin was distributed in relation to sinusoids, portal veins, central veins and granulomas, expressed in stellate cells and myofibroblasts. In the periportal zone, the expression in sinusoids was decreased at 24 h but increased on day 7 after carbon tetrachloride administration. Numbers of epimorphin-expressing cells and proliferating hepatocytes changed in an inverse manner as time progressed. In the pericentral zone, reactivity for epimorphin was markedly enhanced concurrently with appearance of granulomas. Quantities of 34-kDa isoform paralleled epimorphin-staining intensity. In vitro, epimorphin induced spherical hepatocyte aggregates and maintained differentiated hepatocyte function.

Conclusions: Epimorphin is involved in tissue repair following a single injection of carbon tetrachloride, in which distribution and the quantity of epimorphin expression are important, particularly in maintaining hepatocyte function.

MeSH terms

  • Acute Disease
  • Alanine Transaminase / blood
  • Animals
  • Blotting, Western
  • Carbon Tetrachloride*
  • Cell Aggregation / drug effects
  • Cell Proliferation / drug effects
  • Cells, Cultured
  • Chemical and Drug Induced Liver Injury*
  • Female
  • Hepatocytes / drug effects
  • Hepatocytes / metabolism
  • Hepatocytes / pathology
  • Liver Diseases / metabolism
  • Liver Diseases / pathology
  • Liver Diseases / physiopathology*
  • Liver Regeneration*
  • Membrane Glycoproteins / metabolism*
  • Membrane Glycoproteins / pharmacology
  • Mice
  • Mice, Inbred BALB C
  • Protein Isoforms / metabolism
  • Tissue Distribution

Substances

  • Epim protein, mouse
  • Membrane Glycoproteins
  • Protein Isoforms
  • Carbon Tetrachloride
  • Alanine Transaminase