The B isoform of the insulin receptor signals more efficiently than the A isoform in HepG2 cells

J Biol Chem. 1995 Sep 1;270(35):20816-23. doi: 10.1074/jbc.270.35.20816.

Abstract

We have demonstrated previously that dexamethasone treatment of HepG2 cells caused an enhancement of insulin's metabolic effects (Kosaki, A., and Webster, N. J. (1993) J. Biol. Chem. 268, 21990-21996). This correlated with increased expression of the mRNA encoding the B isoform of the insulin receptor (IR). In the present study, we have demonstrated that dexamethasone treatment caused in addition an enhancement in insulin-stimulated immediate-early gene expression (c-fos and egr-1). Dexamethasone treatment caused an increase in in vivo IR autophosphorylation and insulin receptor substrate-1 (IRS-1) phosphorylation both early events in the insulin signaling pathway. Furthermore, the IRS-1 phosphorylation was distinctly left shifted, although the level of IRS-1 protein was unchanged. Total cellular tyrosine phosphatase activity was unaltered when assayed with 32P-labeled IR and IRS-1. Studies in vitro on wheat-germ agglutinin-purified receptors showed that the B isoform of the IR had increased kinase activity both toward itself and the exogenous substrates poly.glu4:tyr1 and recombinant IRS-1 protein. In addition, two-dimensional tryptic phosphopeptide maps indicated that the B isoform has an additional phosphopeptide that is not seen for the A isoform. In conclusion, it appears that the B isoform of the IR signals more efficiently than the A isoform in HepG2 cells.

Publication types

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

MeSH terms

  • Base Sequence
  • DNA Primers
  • DNA-Binding Proteins / biosynthesis
  • Dexamethasone / pharmacology*
  • Early Growth Response Protein 1
  • Gene Expression / drug effects*
  • Genes, Immediate-Early / drug effects*
  • Genes, fos
  • Hepatoblastoma
  • Humans
  • Immediate-Early Proteins*
  • Insulin / metabolism
  • Insulin / pharmacology*
  • Insulin Receptor Substrate Proteins
  • Kinetics
  • Liver Neoplasms
  • Molecular Sequence Data
  • Phosphoproteins / metabolism
  • Phosphorylation
  • Polymerase Chain Reaction
  • Protein Tyrosine Phosphatases / metabolism
  • Proto-Oncogene Proteins c-fos / biosynthesis
  • Receptor, Insulin / biosynthesis
  • Receptor, Insulin / metabolism
  • Receptor, Insulin / physiology*
  • Signal Transduction*
  • Transcription Factors / biosynthesis
  • Tumor Cells, Cultured
  • Zinc Fingers

Substances

  • DNA Primers
  • DNA-Binding Proteins
  • EGR1 protein, human
  • Early Growth Response Protein 1
  • IRS1 protein, human
  • Immediate-Early Proteins
  • Insulin
  • Insulin Receptor Substrate Proteins
  • Phosphoproteins
  • Proto-Oncogene Proteins c-fos
  • Transcription Factors
  • Dexamethasone
  • Receptor, Insulin
  • Protein Tyrosine Phosphatases