Osteopontin promotes inflammation in patients with acute coronary syndrome through its activity on IL-17 producing cells

Eur J Immunol. 2012 Oct;42(10):2803-14. doi: 10.1002/eji.201242475. Epub 2012 Aug 28.

Abstract

Atherosclerosis is a progressive disease with a strong inflammatory component. Here we confirm the existence of a critical imbalance in the ratio of Th17 to Treg-cell populations in peripheral CD4(+) T cells from patients with acute coronary syndrome (ACS), which favors inflammation. This was concurrent with increased IL-17 production from the CD4(+) CD45RA(-) FOXP3(lo) Treg-cell subset, and elevated osteopontin (OPN) levels in serum from ACS patients. We demonstrate a direct effect of OPN in serum from ACS patients on increased IL-17 production by CD4(+) CD45RA(-) FOXP3(lo) T cells, mediated through recruitment of the OPN receptors CD29 and CD44, and dependent on STAT3 and the nuclear hormone receptor retinoic-acid-related orphan receptor-γt (RORγt) pathway, but not IL-6 production. To our knowledge and beyond the disease context of ACS, this study constitutes the first demonstration of a critical role for OPN in the positive regulation of inflammation through increased IL-17 production by CD4(+) CD45RA(-) FOXP3(lo) cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Coronary Syndrome / immunology*
  • Aged
  • CD4-Positive T-Lymphocytes / immunology*
  • Cells, Cultured
  • Female
  • Forkhead Transcription Factors / metabolism
  • Humans
  • Inflammation / immunology*
  • Interleukin-17 / genetics
  • Interleukin-17 / metabolism*
  • Leukocyte Common Antigens / metabolism
  • Male
  • Middle Aged
  • Nuclear Receptor Subfamily 1, Group F, Member 3 / metabolism
  • Osteopontin / biosynthesis*
  • Osteopontin / blood
  • Osteopontin / genetics
  • STAT3 Transcription Factor / metabolism
  • Signal Transduction
  • T-Lymphocytes, Regulatory / immunology*
  • Th17 Cells / immunology*
  • Up-Regulation

Substances

  • FOXP3 protein, human
  • Forkhead Transcription Factors
  • Interleukin-17
  • Nuclear Receptor Subfamily 1, Group F, Member 3
  • STAT3 Transcription Factor
  • Osteopontin
  • Leukocyte Common Antigens