IL-17 increases cadherin-11 expression in a model of autoimmune experimental arthritis and in rheumatoid arthritis

Immunol Lett. 2011 Oct 30;140(1-2):97-103. doi: 10.1016/j.imlet.2011.07.003. Epub 2011 Jul 20.

Abstract

IL-17 plays important roles in synovial inflammation and bone destruction in the mouse model of autoimmune arthritis and in rheumatoid arthritis (RA). Cadherin-11 determines the behavior of synovial cells in their proinflammatory and destructive tissue response in inflammatory arthritis, and promotes the invasive behavior of fibroblast-like synoviocytes (FLS). The purpose of this study was to examine the effect of IL-17 on the expression of cadherin-11 in autoimmune experimental arthritis and in RA synovium. The severity of synovial inflammation and bone destruction were examined in IL-17-injected knee joints of mice with collagen-induced arthritis (CIA). Cadherin-11 expression was examined in the synovium of mice with CIA, of IL-1 receptor antagonist (IL-1Ra)-deficient mice and of patients with RA and osteoarthritis (OA). Cadherin-11 expression was also examined in the synovium of IL-17 injected knee joints from CIA mice and in IL-17-stimulated FLS of CIA mice and RA patients. IL-17 aggravated synovial inflammation and bone destruction in CIA. By immunohistochemistry, cadherin-11 expression was increased in the synovium of mice with CIA and IL-1Ra-deficient mice and in patients with RA. Synovial cadherin-11 expression in IL-17-injected knee joints, measured by real-time RT-PCR, Western blot and immunohistochemistry, was increased in CIA. Cadherin-11 expression was significantly increased by IL-17 in cultured FLS of CIA mice and RA patients, and these increases were blocked by NF-κB inhibitors. IL-17 increased the expression of cadherin-11 in vivo and in vitro, which implies that an IL-17-induced increase of cadherin-11 is involved in IL-17-induced aggravation of joint destruction and inflammation.

MeSH terms

  • Animals
  • Arthritis, Experimental / chemically induced
  • Arthritis, Experimental / immunology*
  • Arthritis, Rheumatoid / immunology*
  • Autoimmunity
  • Cadherins / genetics
  • Cadherins / immunology
  • Cadherins / metabolism*
  • Cells, Cultured
  • Collagen / administration & dosage
  • Disease Models, Animal
  • Disease Progression
  • Humans
  • Interleukin 1 Receptor Antagonist Protein / genetics
  • Interleukin-17 / administration & dosage*
  • Mice
  • Mice, Knockout
  • Synovial Membrane / drug effects*
  • Synovial Membrane / metabolism

Substances

  • Cadherins
  • Interleukin 1 Receptor Antagonist Protein
  • Interleukin-17
  • osteoblast cadherin
  • Collagen