Open AccessInterleukin‐1β‐stimulated invasion of articular cartilage by rheumatoid synovial fibroblasts is inhibited by antibodies to specific integrin receptors and by collagenase inhibitors
Author(s) -
Wang Allan Z.,
Wang Jane C.,
Fisher Gregory W.,
Diamond Herbert S.
Publication year - 1997
Publication title -
arthritis & rheumatism
Language(s) - English
Resource type - Journals
eISSN - 1529-0131
pISSN - 0004-3591
DOI - 10.1002/art.1780400715
Subject(s) - collagenase , cartilage , integrin , chemistry , in vivo , receptor , interstitial collagenase , in vitro , antibody , microbiology and biotechnology , immunology , biology , anatomy , biochemistry , enzyme
Objective . To study the role of integrin receptors in the invasion of cartilage by rheumatoid synovial fibroblasts (RSF). Methods . RSF were cocultured with cartilage slices alone or in the presence of various potential activators or inhibitors. The penetration of the cartilage surface by RSF was determined by live‐cell imaging of fluorescent‐labeled cells. Results . Interleukin‐1β (IL‐1β) and IL‐8 stimulated the RSF invasion of cartilage. Invasion was specific for RSF and required a concentration gradient of IL‐1β. The IL‐1β‐activated invasion of cartilage was inhibited by anti‐IL‐1 antibodies, IL‐1 receptor antagonist, and collagenase inhibitors. RSF invasion was also inhibited by antibodies to α4, α5, αV, and β1 integrins. Conclusion . In this study, an IL‐1β concentration gradient was required for RSF invasion into cartilage, raising the possibility that in vivo invasion may be induced by IL‐1β released by chondrocytes. The IL‐1β activation of RSF assayed in vitro may contribute to the RSF invasion of cartilage in vivo. Cartilage invasion requires the availability of β1 and α4, α5, and αV integrins and the presence of collagenase activity.