Expression and proinflammatory role of proteinase-activated receptor 2 in rheumatoid synovium - Ex vivo studies using a novel proteinase-activated receptor 2 antagonist

Objective. Serine proteinases activate the G protein-coupled receptor, proteinase-activated receptor 2 (PAR-2), via cleavage and exposure of a tethered ligand. PAR-2 is known to exert proinflammatory actions in a murine model of arthritis, since PAR-2deficient mice exhibit strikingly reduced articular inflammation. This study was undertaken to examine synovial PAR-2 expression and to determine the effect of a novel PAR-2 antagonist on synovial cylokine production, in order to investigate the hypothesis that PAR-2 plays a critical role in the pathogenesis of rheumatoid arthritis (RA). Methods. Using a monoclonal antibody to human PAR-2, expression in RA synovium and cultured synovial fibroblasts was characterized. The novel PAR-2 antagonist, ENNID-1068, was added to primary cultures of RA synovial tissue, from which spontaneous cytokine release was measured. Results. PAR-2 was substantially up-regulated inRA synovium compared with control synovial tissue from patients with osteoarthritis or seronegative inflammatory arthritis, neither of which exhibited significant PAR-2 expression. Importantly, spontaneous release of tumor necrosis factor a and interleukin-113 from RA synovium was substantially inhibited by ENMD-1068, in a dose-dependent manner. Conclusion. These findings identify PAR-2 as a novel upstream regulator of proinflammatory cytokine production in RA and indicate its potential as a novel therapeutic target in inflammatory arthritis.