Resveratrol inhibits macrophage expression of EMMPRIN by activating PPARgamma

Vascul Pharmacol. 2007 Feb;46(2):114-21. doi: 10.1016/j.vph.2006.08.412. Epub 2006 Sep 3.

Abstract

The effect of resveratrol on macrophage EMMPRIN expression and its potential mechanism was investigated. Both EMMPRIN expression and MMP-9 activity, respectively assayed by Western blot and zymography, were greatly up-regulated during PMA-induced macrophage differentiation from THP-1 monocytes. Both resveratrol and a PPARgamma agonist, pioglitazone, significantly inhibited EMMPRIN expression and MMP-9 activity in a concentration-dependent manner. The effects of pioglitazone and resveratrol were reversed by pretreatment of THP-1 cells with a PPARgamma antagonist, GW9662, prior to PMA induction. Thus, data suggest that resveratrol may down-regulate EMMPRIN and MMP-9 through PPARgamma activation. This possibility was further examined in resveratrol-or pioglitazone-treated U937 cells, which had been co-transfected with a PPARgamma expression vector and a luciferase reporter vector containing three tandem repeats of PPRE in cis. Results of the agonist-activated luciferase assay showed that resveratrol activated PPARgamma in a concentration-dependent manner. Since EMMPRIN and MMP-9 up-regulation is associated with activation of the NF-kappaB pathway, we investigated the effect of pioglitazone and resveratrol on TNF-alpha-induced NF-kappaB activation. Western blot results indicated that both pioglitazone and resveratrol markedly inhibited the NF-kappaB pathway through suppressing IkappaB protein phosphorylation in macrophages, although this effect of resveratrol was not reversed by GW9662. In conclusion, resveratrol can down-regulate EMMPRIN expression by macrophages via activating PPARgamma. This may be a primary mechanism of its inhibitory effect on MMP-9.

MeSH terms

  • Anilides / pharmacology
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology*
  • Basigin / biosynthesis*
  • Cell Differentiation / drug effects
  • Dose-Response Relationship, Drug
  • Gene Expression Regulation / drug effects
  • Humans
  • I-kappa B Proteins / metabolism
  • Macrophages / cytology
  • Macrophages / drug effects*
  • Macrophages / metabolism
  • Matrix Metalloproteinase 9 / biosynthesis*
  • Monocytes / drug effects
  • Monocytes / metabolism
  • NF-kappa B / metabolism
  • PPAR gamma / agonists*
  • PPAR gamma / genetics
  • PPAR gamma / metabolism
  • Phosphorylation
  • Pioglitazone
  • Promoter Regions, Genetic / drug effects
  • Resveratrol
  • Stilbenes / pharmacology*
  • Tetradecanoylphorbol Acetate / pharmacology
  • Thiazolidinediones / pharmacology
  • Time Factors
  • Transfection
  • Tumor Necrosis Factor-alpha / pharmacology
  • U937 Cells

Substances

  • 2-chloro-5-nitrobenzanilide
  • Anilides
  • Anti-Inflammatory Agents, Non-Steroidal
  • BSG protein, human
  • I-kappa B Proteins
  • NF-kappa B
  • PPAR gamma
  • Stilbenes
  • Thiazolidinediones
  • Tumor Necrosis Factor-alpha
  • Basigin
  • Matrix Metalloproteinase 9
  • Tetradecanoylphorbol Acetate
  • Resveratrol
  • Pioglitazone