Calcineurin mediates the calcium-dependent inhibition of adipocyte differentiation in 3T3-L1 cells

J Biol Chem. 2002 Dec 20;277(51):49776-81. doi: 10.1074/jbc.M207913200. Epub 2002 Sep 25.

Abstract

Recent studies have revealed that the calcium-dependent serine/threonine phosphatase calcineurin mediates the effects of intracellular calcium in many different cell types. In this study we investigated the role of calcineurin in the regulation of adipocyte differentiation. We found that the specific calcineurin inhibitors cyclosporin A and FK506 overcame the antiadipogenic effect of calcium ionophore on the differentiation of 3T3-L1 preadipocytes. This finding suggests that calcineurin is responsible for mediating the previously documented Ca(2+)-dependent inhibition of adipogenesis. We further demonstrate that the expression of a constitutively active calcineurin mutant potently inhibits the ability of 3T3-L1 cells to undergo adipocyte differentiation by preventing expression of the proadipogenic transcription factors peroxisome proliferator-activated receptor gamma (PPARgamma) and CCAAT/enhancer-binding protein alpha (C/EBPalpha). This calcineurin-mediated block in adipocyte differentiation is rescued by ectopic expression of PPARgamma1. Finally, we demonstrate that inhibition of endogenous calcineurin activity with either FK506 or a specific calcineurin inhibitory peptide enhances differentiation of 3T3-L1 cells in response to suboptimal adipogenic stimuli, suggesting that endogenous calcineurin activity normally sets a signaling threshold that antagonizes efficient adipocyte differentiation. Collectively, these data indicate that calcineurin acts as a Ca(2+)-dependent molecular switch that negatively regulates commitment to adipocyte differentiation by preventing the expression of critical proadipogenic transcription factors.

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
  • Blotting, Northern
  • CCAAT-Enhancer-Binding Protein-alpha / metabolism
  • CCAAT-Enhancer-Binding Protein-beta / metabolism
  • CCAAT-Enhancer-Binding Protein-delta
  • CCAAT-Enhancer-Binding Proteins / metabolism
  • Calcineurin / metabolism*
  • Calcium / metabolism
  • Cell Differentiation
  • Cyclosporine / pharmacology
  • Flow Cytometry
  • Immunoblotting
  • Immunosuppressive Agents / pharmacology
  • Mice
  • Receptors, Cytoplasmic and Nuclear / metabolism
  • Retroviridae / genetics
  • Tacrolimus / pharmacology
  • Transcription Factors / metabolism
  • Transcription, Genetic

Substances

  • CCAAT-Enhancer-Binding Protein-alpha
  • CCAAT-Enhancer-Binding Protein-beta
  • CCAAT-Enhancer-Binding Proteins
  • Cebpd protein, mouse
  • Immunosuppressive Agents
  • Receptors, Cytoplasmic and Nuclear
  • Transcription Factors
  • CCAAT-Enhancer-Binding Protein-delta
  • Cyclosporine
  • Calcineurin
  • Calcium
  • Tacrolimus