Bi-directional regulation of brown fat adipogenesis by the insulin receptor

J Biol Chem. 2003 Aug 29;278(35):33377-83. doi: 10.1074/jbc.M303056200. Epub 2003 Jun 13.

Abstract

Insulin is a potent inducer of adipogenesis, and differentiation of adipocytes requires many components of the insulin signaling pathway, including the insulin receptor substrate IRS-1 and phosphatidylinositol 3-kinase (PI3K). Brown pre-adipocytes in culture exhibit low levels of insulin receptor (IR), and during differentiation there is both an increase in total IR levels and a shift in the alternatively spliced forms of IR from the A isoform (-exon 11) to the B isoform (+exon 11). Brown pre-adipocyte cell lines from insulin receptor-deficient mice exhibit dramatically impaired differentiation and an inability to regulate alternative splicing of the insulin receptor. Surprisingly, re-expression of either splice isoform of IR in the IR-deficient cells fails to rescue differentiation in these cells. Likewise, overexpression of IR in control IRlox cells also results in inhibition of differentiation and a failure to accumulate expression of the adipogenic markers peroxisome proliferator-activated receptor gamma, Glut4, and fatty acid synthase, although cells overexpressing IR retain the ability to activate PI3K and down-regulate mitogen-activated protein kinase (MAPK) phosphorylation. Thus, differentiation of brown adipocytes requires a timed and regulated expression of IR, and either the absence or overabundance of insulin receptors in these cells dramatically inhibits differentiation.

Publication types

  • Retracted Publication

MeSH terms

  • Adipocytes / cytology*
  • Adipocytes / metabolism*
  • Adipose Tissue, Brown / metabolism*
  • Alternative Splicing
  • Animals
  • Azo Compounds / pharmacology
  • Cell Differentiation
  • Coloring Agents / pharmacology
  • Down-Regulation
  • Exons
  • Glucose Transporter Type 4
  • Homozygote
  • Immunoblotting
  • Insulin / metabolism
  • Insulin Receptor Substrate Proteins
  • MAP Kinase Signaling System
  • Mice
  • Mice, Knockout
  • Monosaccharide Transport Proteins / metabolism
  • Muscle Proteins*
  • Phosphatidylinositol 3-Kinases / metabolism
  • Phosphoproteins / metabolism
  • Phosphorylation
  • Plasmids / metabolism
  • Precipitin Tests
  • Protein Isoforms
  • Receptor, Insulin / chemistry
  • Receptor, Insulin / genetics
  • Receptor, Insulin / metabolism*
  • Retroviridae / genetics
  • Retroviridae / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Signal Transduction
  • Time Factors

Substances

  • Azo Compounds
  • Coloring Agents
  • Glucose Transporter Type 4
  • Insulin
  • Insulin Receptor Substrate Proteins
  • Irs1 protein, mouse
  • Monosaccharide Transport Proteins
  • Muscle Proteins
  • Phosphoproteins
  • Protein Isoforms
  • Slc2a4 protein, mouse
  • Phosphatidylinositol 3-Kinases
  • Receptor, Insulin
  • oil red O