期刊
CHEMBIOCHEM
卷 15, 期 8, 页码 1154-1160出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/cbic.201300754
关键词
biochromatography; isothermal titration calorimetry; PPARs; resveratrol; transactivation assays; X-ray crystallography
资金
- Intramural Research Program of the National Institute on Aging, National Institutes of Health
- Ministero dell'Istruzione, dell'Universita e della Ricerca [PRIN 2009K7R7NA]
- Ministero dell'Universita e della Ricerca Scientifica [2009Z8YTYC]
Resveratrol, a modulator of several signaling proteins, can exert off-target effects involving the peroxisome proliferator-activated receptor (PPAR) transcription factors. However, evidence for the direct interaction between this polyphenol and PPARs is lacking. Here, we addressed the hypothesis that resveratrol and its metabolites control aspects of PPAR transcriptional activity through direct interaction with PPARs. Bioaffinity chromatographic studies with the immobilized ligand-binding domains (LBDs) of PPAR and PPAR and isothermal titration calorimetry allowed the binding affinities of resveratrol, resveratrol 3-O-glucuronide, resveratrol 4-O-glucuronide, and resveratrol 3-O-sulfate to both PPAR-LBDs to be determined. Interaction of resveratrol, resveratrol 3-O-glucuronide, and resveratrol 4-O-glucuronide with PPAR-LBD occurred with binding affinities of 1.4, 1.1, and 0.8 mu M, respectively, although only resveratrol bound to the PPAR alpha-LBD with a binding affinity of 2.7 mu M. Subsequently, X-ray crystallographic studies were carried out to characterize resveratrol binding to the PPAR gamma-LBD at the molecular level. The electron density map from the crystal structure of the complex between PPAR gamma-LBD and resveratrol revealed the presence of one molecule of resveratrol bound to the LBD of PPAR gamma, with the ligand occupying a position close to that of other known PPAR gamma ligands. Transactivation assays were also performed in HepG2 cells, with the results showing that resveratrol was not a PPAR agonist but instead was able to displace rosiglitazone from PPAR gamma and Wy-14643 from PPAR alpha with IC50 values of (27.4 +/- 1.8) mu M and (31.7 +/- 2.5) mu M, respectively. We propose that resveratrol acts as a PPAR antagonist through its direct interaction with PPAR gamma and PPAR alpha.
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