Inhibition of adipogenesis through MAP kinase-mediated phosphorylation of PPARgamma

Science. 1996 Dec 20;274(5295):2100-3. doi: 10.1126/science.274.5295.2100.

Abstract

Adipocyte differentiation is an important component of obesity and other metabolic diseases. This process is strongly inhibited by many mitogens and oncogenes. Several growth factors that inhibit fat cell differentiation caused mitogen-activated protein (MAP) kinase-mediated phosphorylation of the dominant adipogenic transcription factor peroxisome proliferator-activated receptor gamma (PPARgamma) and reduction of its transcriptional activity. Expression of PPARgamma with a nonphosphorylatable mutation at this site (serine-112) yielded cells with increased sensitivity to ligand-induced adipogenesis and resistance to inhibition of differentiation by mitogens. These results indicate that covalent modification of PPARgamma by serum and growth factors is a major regulator of the balance between cell growth and differentiation in the adipose cell lineage.

Publication types

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

MeSH terms

  • 3T3 Cells
  • Adipocytes / cytology*
  • Adipocytes / metabolism
  • Animals
  • Blood
  • Calcium-Calmodulin-Dependent Protein Kinases / antagonists & inhibitors
  • Calcium-Calmodulin-Dependent Protein Kinases / metabolism*
  • Cell Differentiation
  • Cell Line
  • Enzyme Inhibitors / pharmacology
  • Epidermal Growth Factor / pharmacology
  • Flavonoids / pharmacology
  • Insulin / pharmacology
  • Ligands
  • Mice
  • Mitogens / pharmacology
  • Mutation
  • Phosphorylation
  • Rats
  • Receptors, Cytoplasmic and Nuclear / chemistry
  • Receptors, Cytoplasmic and Nuclear / genetics
  • Receptors, Cytoplasmic and Nuclear / metabolism*
  • Tetradecanoylphorbol Acetate / pharmacology
  • Transcription Factors / chemistry
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*
  • Transcription, Genetic / drug effects
  • Transfection

Substances

  • Enzyme Inhibitors
  • Flavonoids
  • Insulin
  • Ligands
  • Mitogens
  • Receptors, Cytoplasmic and Nuclear
  • Transcription Factors
  • Epidermal Growth Factor
  • Calcium-Calmodulin-Dependent Protein Kinases
  • Tetradecanoylphorbol Acetate
  • 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one