Regulation of adipogenesis by natural and synthetic REV-ERB ligands

Naresh Kumar, Laura A. Solt, Yongjun Wang, Pamela M. Rogers, Gargi Bhattacharyya, Theodore M. Kamenecka, Keith R. Stayrook, Christine Crumbley, Z. Elizabeth Floyd, Jeffrey M. Gimble, Patrick R. Griffin, Thomas P. Burris

Research output: Contribution to journalArticlepeer-review

107 Scopus citations


The nuclear hormone receptor, REV-ERB, plays an essential role in adipogenesis. Rev-erbα expression is induced in 3T3-L1 cells during adipogenesis, and overexpression of this receptor leads to expression of adipogenic genes. We recently demonstrated that the porphyrin heme functions as a ligand for REV-ERB, and binding of heme is required for the receptor's activity. We therefore hypothesized that REV-ERB ligands may play a role in regulation of adipogenesis. We detected an increase intracellular heme levels during 3T3-L1 adipogenesis that correlated with induction of aminolevulinic acid synthase 1 (Alas1) expression, the rate-limiting enzyme in heme biosynthesis. If the increase in Alas1 expression was blocked, adipogenesis was severely attenuated, indicating that induction of expression of Alas1 and the increase in heme synthesis is critical for differentiation. Inhibition of heme synthesis during adipogenesis leads to decreased recruitment of nuclear receptor corepressor to the promoter of a REV-ERB target gene, suggesting alteration of REV-ERB activity. Treatment of 3T3-L1 cells with a synthetic REV-ERB ligand, SR6452, resulted in induction of adipocyte differentiation to a similar extent as treatment with the peroxisomal proliferator-activated receptor-γ agonist, rosiglitazone. Combination of SR6452 and rosiglitazone had an additive effect on stimulation of adipocyte differentiation. These results suggest that heme, functioning as a REV-ERB ligand, is an important signaling molecule for induction of adipogenesis. Moreover, synthetic small molecule ligands for REV-ERB are effective modulators of adipogenesis and may be useful for treatment of metabolic diseases.

Original languageEnglish (US)
Pages (from-to)3015-3025
Number of pages11
Issue number7
StatePublished - Jul 2010

All Science Journal Classification (ASJC) codes

  • Endocrinology


Dive into the research topics of 'Regulation of adipogenesis by natural and synthetic REV-ERB ligands'. Together they form a unique fingerprint.

Cite this