Mutated insulin receptor Val996 reduces insulin-dependent generation of inositol glycan and diacylglycerol

Diabetes. 1992 Nov;41(11):1373-9. doi: 10.2337/diab.41.11.1373.

Abstract

We evaluated whether insulin-receptor tyrosine kinase activity is required for activation of PDH, insulin-induced hydrolysis of PIG and generation of IG and 1,2-DAG. For the analysis, we used stable-transfected CHO cell lines expressing wild-type human insulin receptor (CHO-wt cells) or the mutant receptor (Val996) that lacks tyrosine kinase activity (CHO-mut cells) (1,2). Insulin stimulated PDH activity in three CHO cell lines in a dose-dependent manner. Half-maximal concentrations of insulin to activate PDH was 7 x 10(-11) M in the CHO-wt cells, 10(-9) M in the parental cells, and 8 x 10(-9) M in the CHO-mut cells. Insulin stimulated hydrolysis of PIG and generation of IG and DAG in three CHO cell lines in a dose-dependent manner. Half-maximal concentrations of insulin to induce generation of IG was 8 x 10(-11) M in the CHO-wt cells, 10(-9) M in the parental CHO cells, and 10(-8) M in the CHO-mut cells. ED50 for the stimulation of DAG generation was 7 x 10(-11) M in the CHO-wt cells, 10(-9) M in the parental cells, and 10(-8) M in the CHO-mut cells. It is concluded that insulin-dependent PDH activation, PIG hydrolysis, and IG and DAG generation are mediated by the wild-type but not by the mutated insulin receptor of Val996. This study suggests that tyrosine kinase activity of the insulin receptor might be a prerequisite for insulin-stimulated generation of IG and DAG.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • CHO Cells
  • Cricetinae
  • Diglycerides / biosynthesis*
  • Glycosylphosphatidylinositols
  • Humans
  • Insulin / pharmacology*
  • Kinetics
  • Mutagenesis, Site-Directed
  • Phosphatidylinositols / biosynthesis*
  • Polysaccharides / biosynthesis*
  • Protein-Tyrosine Kinases / genetics
  • Protein-Tyrosine Kinases / metabolism*
  • Pyruvate Dehydrogenase Complex / metabolism
  • Receptor, Insulin / genetics
  • Receptor, Insulin / metabolism*
  • Transfection
  • Valine*

Substances

  • Diglycerides
  • Glycosylphosphatidylinositols
  • Insulin
  • Phosphatidylinositols
  • Polysaccharides
  • Pyruvate Dehydrogenase Complex
  • Protein-Tyrosine Kinases
  • Receptor, Insulin
  • Valine