Regulation of adipogenesis by nuclear receptor PPARγ is modulated by the histone demethylase JMJD2C

Fernando Lizcano, Carolina Romero, Diana Vargas

Research output: Contribution to journalArticlepeer-review

26 Scopus citations


A potential strategy to combat obesity and its associated complications involves modifying gene expression in adipose cells to reduce lipid accumulation. The nuclear receptor Peroxisome Proliferator-activated receptor gamma (PPARγ) is the master regulator of adipose cell differentiation and its functional activation is currently used as a therapeutic approach for Diabetes Mellitus type 2. However, total activation of PPARγ induces undesirable secondary effects that might be set with a partial activation. A group of proteins that produce histone demethylation has been shown to modify the transcriptional activity of nuclear receptors. Here we describe the repressive action of the jumonji domain containing 2C/lysine demethylase 4 C (JMJD2C/KDM4C) on PPARγ transcriptional activation. JMJD2C significantly reduced the rosiglitazone stimulated PPARγ activation. This effect was mainly observed in experiments performed using the Tudor domains that may interact with histone deacetylase class 1 (HDAC) and this interaction probably reduces the mediated activation of PPARγ. Trichostatin A, a HDAC inhibitor, reduces the repressive effect of JMJD2C. When JMJD2C was over-expressed in 3T3-L1 cells, a reduction of differentiation was observed with the Tudor domain. In summary, we herein describe JMJD2C-mediated reduction of PPARgamma transcriptional activation as well as preadipocyte differentiation. This novel action of JMJD2C might have an important role in new therapeutic approaches to treat obesity and its complications.

Original languageEnglish (US)
Pages (from-to)19-24
Number of pages6
JournalGenetics and Molecular Biology
Issue number1
StatePublished - 2011
Externally publishedYes


  • Adipocyte
  • Deacetylation
  • Demethylation
  • Histones
  • Jmjd2c
  • PPARγ
  • Trichostatin a

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics


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