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Role of osteopontin in amplification and perpetuation of rheumatoid synovitis.

Authors :
Xu, Guangwu
Nie, Hong
Li, Ningli
Zheng, Wenxin
Zhang, Dongqing
Feng, Guozhang
Ni, Liqing
Xu, Rong
Hong, Jian
Zhang, Jingwu Z.
Source :
Journal of Clinical Investigation. Apr2005, Vol. 115 Issue 4, p1060-1067. 8p. 2 Black and White Photographs, 2 Charts, 8 Graphs.
Publication Year :
2005

Abstract

Osteopontin (OPN) is an extracellular matrix protein of pleiotropic properties and has been recently recognized as a potential inflammatory cytokine. In this study, we demonstrate, for the first time to our knowledge, that overexpression of OPN in synovial T cells is associated with local inflammatory milieu and that OPN acts as an important mediator in amplification and perpetuation of rheumatoid synovitis. The study revealed that mRNA expression of OPN was highly elevated in CD4+ synovial T cells derived from patients with RA, which correlated with increased OPN concentrations in synovial fluid (SF). The pattern of OPN overexpression was confined to rheumatoid synovium and correlated with coexpression of selected OPN receptors in synovial T cells, including integrins αv and β1 and CD44. RA-derived SF stimulated the expression of OPN in T cells, which was attributable to IL-10 present in SF and abrogated by anti-IL-10 antibody. Among the more than 300 autoimmune and inflammatory response genes examined, OPN selectively induced the expression of proinflammatory cytokines and chemokines known to promote migration and recruitment of inflammatory cells. Furthermore, it was evident that OPN activated transcription factor NF-κB in mononuclear cells. The study has important implications for understanding the role of OPN in rheumatoid synovitis and other inflammatory conditions. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00219738
Volume :
115
Issue :
4
Database :
Academic Search Index
Journal :
Journal of Clinical Investigation
Publication Type :
Academic Journal
Accession number :
16624381
Full Text :
https://doi.org/10.1172/JCI200523273