Interleukin-10 and Th2 cytokines differentially regulate osteopontin expression in human monocytes and dendritic cells

J Interferon Cytokine Res. 2006 Aug;26(8):562-7. doi: 10.1089/jir.2006.26.562.

Abstract

Osteopontin (OPN) is a pleiotrophic phosphoprotein involved in homeostatic and pathophysiologic responses. It is known to be a chemotactic cytokine for dendritic cells (DCs), a critical cell type in both innate and adaptive immune responses. We report herein a contrasting role of interleukin-10 (IL-10) and Th2 cytokines in the regulation of OPN expression in human monocytes and monocyte-derived DCs (Mo-DCs). Our results showed first that the expression of OPN in monocytes and Mo-DCs was induced in a time-dependent and dose-dependent manner by IL-10 but was inhibited by IL-4 or IL-13. Further, the basal level of OPN expression was also inhibited by IL-4. This inhibitory effect of IL-4 was associated with a faster decay of OPN transcripts and a decreased proximal promoter activity of OPN in IL-4-treated cells. These results demonstrate a novel role of IL-10 and Th2 cytokines in the regulation of DC function through their contrasting regulatory activities on the expression of OPN.

MeSH terms

  • Dendritic Cells / drug effects
  • Dendritic Cells / immunology*
  • Gene Expression Regulation
  • Humans
  • Interleukin-10 / pharmacology*
  • Interleukin-13 / pharmacology
  • Interleukin-4 / pharmacology
  • Interleukins / pharmacology*
  • Monocytes / drug effects
  • Monocytes / immunology*
  • Osteopontin
  • RNA Stability / drug effects
  • RNA, Messenger / metabolism
  • Sialoglycoproteins / genetics*
  • Sialoglycoproteins / metabolism
  • Th2 Cells / immunology

Substances

  • Interleukin-13
  • Interleukins
  • RNA, Messenger
  • SPP1 protein, human
  • Sialoglycoproteins
  • Osteopontin
  • Interleukin-10
  • Interleukin-4