Interleukin-10 is upregulated by nanomolar rosiglitazone treatment of mature dendritic cells and human CD4+ T cells

Cytokine. 2007 Sep;39(3):184-91. doi: 10.1016/j.cyto.2007.07.191. Epub 2007 Sep 5.

Abstract

Activators of peroxisome proliferator-activated receptor (PPAR)-gamma are anti-inflammatory and have been proposed as therapeutic agents for the treatment of Th1-type inflammatory diseases. We report that nanomolar concentrations of rosiglitazone enhance the production of IL-10 from activated human mature monocyte-derived dendritic cells. Also, rosiglitazone specifically induces the production of IL-10 from TCR-activated human CD4+ T cells and that this effect is PPAR-gamma-dependent. We also demonstrate for the first time the presence of a functional PPAR response element (PPRE) in the human IL-10 promoter region. Finally we show that rosiglitazone can induce IL-10 in combination with 1,25 alpha-dihydroxyvitamin D3 to a greater extent than each treatment alone. In summary our findings demonstrate that IL-10 is upregulated by nanomolar TZDs in immune cells, and this may, in part, be responsible for the potential anti-inflammatory effects of PPAR-gamma in humans.

MeSH terms

  • CD4-Positive T-Lymphocytes / drug effects*
  • CD4-Positive T-Lymphocytes / immunology
  • CD4-Positive T-Lymphocytes / metabolism
  • Cells, Cultured
  • Cholecalciferol / pharmacology
  • Dendritic Cells / drug effects*
  • Dendritic Cells / immunology
  • Dendritic Cells / metabolism
  • Dose-Response Relationship, Drug
  • Drug Synergism
  • Humans
  • Interleukin-10 / biosynthesis*
  • Interleukin-10 / genetics
  • PPAR gamma / agonists
  • PPAR gamma / genetics
  • PPAR gamma / physiology
  • Promoter Regions, Genetic / drug effects
  • Rosiglitazone
  • Thiazolidinediones / pharmacology*
  • Up-Regulation / drug effects*
  • Up-Regulation / genetics
  • Up-Regulation / immunology

Substances

  • PPAR gamma
  • Thiazolidinediones
  • Rosiglitazone
  • Interleukin-10
  • Cholecalciferol