Ornithine decarboxylase induction during liver regeneration in IRS-1-deficient mice

Biochem Biophys Res Commun. 1995 Nov 2;216(1):284-90. doi: 10.1006/bbrc.1995.2622.

Abstract

We investigated the induction of ornithine decarboxylase during liver regeneration after partial hepatectomy in IRS-1-deficient mice. There were no significant differences in ODC activity or the time course of changes in ODC activity between IRS-1-deficient mice and wild-type mice. PI 3'-kinase activity showed similar increases in both groups of mice. Furthermore, ODC induction in IRS-1 transfected CHO cells was studied after stimulation by addition of FCS. The maximal ODC activity was 2.5-fold greater in IRS-1-transfected CHO cells than in control CHO cells. Our results suggest that the IRS-1 pathway may be involved in ODC induction. The absence of a difference in ODC and PI 3'-kinase activity in the regenerating liver between IRS-1-deficient mice and wild-type mice may have been related to the compensatory effects of IRS-2/pp190 [Araki et al. Nature (1994) 372, 186-190; Tobe et al. J.Biol.Chem. (1995) 270, 5698-5701].

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • CHO Cells
  • Cricetinae
  • Enzyme Induction
  • Hepatectomy
  • Humans
  • Insulin Receptor Substrate Proteins
  • Liver / enzymology*
  • Liver Regeneration*
  • Mice
  • Mice, Knockout
  • Mice, Mutant Strains
  • Ornithine Decarboxylase / biosynthesis*
  • Phosphoproteins / biosynthesis
  • Phosphoproteins / deficiency*
  • Phosphoproteins / metabolism
  • Receptor, Insulin / biosynthesis
  • Receptor, Insulin / metabolism
  • Recombinant Proteins / biosynthesis
  • Recombinant Proteins / metabolism
  • Transfection

Substances

  • IRS1 protein, human
  • Insulin Receptor Substrate Proteins
  • Irs1 protein, mouse
  • Phosphoproteins
  • Recombinant Proteins
  • Receptor, Insulin
  • Ornithine Decarboxylase