Open AccessThe role of oncostatin M in animal and human connective tissue collagen turnover and its localization within the rheumatoid joint
Author(s) -
Cawston T. E.,
Curry V. A.,
Summers C. A.,
Clark I. M.,
Riley G. P.,
Life P. F.,
Spaull J. R.,
Goldring M. B.,
Koshy P. J. T.,
Rowan A. D.,
Shingleton W. D.
Publication year - 1998
Publication title -
arthritis & rheumatism
Language(s) - English
Resource type - Journals
eISSN - 1529-0131
pISSN - 0004-3591
DOI - 10.1002/1529-0131(199810)41:10<1760::aid-art8>3.0.co;2-m
Subject(s) - oncostatin m , connective tissue , rheumatoid arthritis , medicine , pathology , immunology , inflammation , interleukin 6
Objective To study the interaction of interleukin‐1α (IL‐1α) and oncostatin M (OSM) in promoting cartilage collagen destruction. Methods Bovine, porcine, and human cartilage and human chondrocytes were studied in culture. The levels of collagenase (matrix metalloproteinase 1 [MMP‐1]) and tissue inhibitor of metalloproteinases 1 (TIMP‐1) were measured by bioassay and enzyme‐linked immunosorbent assay (ELISA). The levels of OSM in rheumatoid synovial fluid were measured by ELISA. Results When combined with OSM, IL‐1α IL‐1β, and tumor necrosis factor α released proteoglycan and collagen from cartilage. OSM was the only member of the IL‐6 family to have this effect. Human tendon also responded to IL‐1α and OSM. OSM increased the production of MMP‐1 and TIMP‐1 but when combined with IL‐1α, synergistically promoted MMP‐1 production in human chondrocytes and synovial fibroblasts. High levels of OSM were found in human rheumatoid synovial fluids, and confocal microscopy showed that OSM was produced by macrophages in rheumatoid synovial tissue. Conclusion These results highlight an important new mechanism by which there is irreversible loss of collagen from cartilage.