The orphan nuclear receptor RORalpha restrains adipocyte differentiation through a reduction of C/EBPbeta activity and perilipin gene expression

Mol Endocrinol. 2009 Jun;23(6):759-71. doi: 10.1210/me.2008-0277. Epub 2009 Mar 26.

Abstract

The nuclear receptor-type transcription factor retinoic acid receptor-related orphan receptor alpha (RORalpha) is a multifunctional molecule involved in tissue development and cellular function, such as inflammation, metabolism, and differentiation; however, the role of RORalpha during adipocyte differentiation has not yet been fully understood. Here we show that RORalpha inhibits the transcriptional activity of CCAAT/enhancer-binding protein beta (C/EBPbeta) without affecting its expression, thereby blocking the induction of both PPARgamma and C/EBPalpha, resulting in the suppression of C/EBPbeta-dependent adipogenesis. RORalpha interacted with C/EBPbeta so as to repress both the C/EBPbeta-p300 association and the C/EBPbeta-dependent recruitment of p300 to chromatin. In addition to the inhibitory effect on C/EBPbeta function, RORalpha also prevents the expression of the lipid droplet coating protein gene perilipin by peroxisome proliferators-activated receptor gamma (PPARgamma), acting through the specific mechanism of its promoter. We identified a suppressive ROR-responsive element overlapping the PPAR-responsive element in the perilipin promoter and verified that RORalpha competitively antagonizes the binding of PPARgamma. RORalpha inhibits PPARgamma-dependent adipogenesis along with the repression of perilipin induction. These findings suggest that RORalpha is a novel negative regulator of adipocyte differentiation that acts through dual mechanisms.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3-L1 Cells
  • Adipocytes / cytology*
  • Adipocytes / metabolism*
  • Adipogenesis / genetics
  • Animals
  • CCAAT-Enhancer-Binding Protein-beta / genetics
  • CCAAT-Enhancer-Binding Protein-beta / metabolism*
  • Carrier Proteins
  • Cell Differentiation / genetics*
  • Chromatin / metabolism
  • DNA / metabolism
  • E1A-Associated p300 Protein / metabolism
  • Gene Expression Regulation*
  • Gene Knockdown Techniques
  • Mice
  • Nuclear Receptor Subfamily 1, Group F, Member 1
  • PPAR gamma / metabolism
  • Perilipin-1
  • Phosphoproteins / genetics*
  • Phosphoproteins / metabolism
  • Phosphorylation
  • Promoter Regions, Genetic / genetics
  • Protein Binding
  • Receptors, Cytoplasmic and Nuclear / metabolism*
  • Trans-Activators / metabolism*
  • Transcription, Genetic

Substances

  • CCAAT-Enhancer-Binding Protein-beta
  • Carrier Proteins
  • Chromatin
  • Nuclear Receptor Subfamily 1, Group F, Member 1
  • PPAR gamma
  • Perilipin-1
  • Phosphoproteins
  • Receptors, Cytoplasmic and Nuclear
  • Trans-Activators
  • DNA
  • E1A-Associated p300 Protein
  • Ep300 protein, mouse