The antidiabetic agent thiazolidinedione stimulates the interaction between PPAR gamma and CBP

Biochem Biophys Res Commun. 1997 Nov 7;240(1):61-4. doi: 10.1006/bbrc.1997.7602.

Abstract

The peroxisome proliferator-activated receptor (PPAR) gamma is a member of the nuclear hormone receptor family, which is predominantly expressed on adipocytes and considered to be involved in the process of adipogenesis. The new thiazolidinedione (TZD) compound, T-174, developed as an antidiabetic drug, stimulated the transcription of PPAR gamma and the adipocyte differentiation of 3T3-L1 cells. Interestingly, T-174 induced the interaction between PPAR gamma and CBP (cAMP response element binding protein (CREB) binding protein), a co-factor of various transcription regulators. CBP mRNA was expressed in both preadipocytes and adipocytes. These results suggest that CBP plays a role in the PPAR gamma-mediated signaling pathway activated by TZD, including adipogenesis.

MeSH terms

  • 3T3 Cells
  • Adipocytes / cytology
  • Adipocytes / drug effects
  • Adipocytes / metabolism
  • Animals
  • Carrier Proteins / biosynthesis
  • Carrier Proteins / metabolism*
  • Cell Differentiation / drug effects
  • Citrates / metabolism*
  • Diabetes Mellitus, Type 2 / metabolism
  • Drug Interactions
  • Humans
  • Hypoglycemic Agents / pharmacology*
  • Mice
  • Microbodies / drug effects
  • Microbodies / metabolism*
  • Receptors, Cytoplasmic and Nuclear / drug effects
  • Receptors, Cytoplasmic and Nuclear / metabolism*
  • Thiazoles / pharmacology*
  • Transcription Factors / drug effects
  • Transcription Factors / metabolism*

Substances

  • Carrier Proteins
  • Citrates
  • Hypoglycemic Agents
  • Receptors, Cytoplasmic and Nuclear
  • Thiazoles
  • Transcription Factors
  • citrate-binding transport protein