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Oncostatin M stimulates monocyte chemoattractant protein-1- and interleukin-1-induced matrix metalloproteinase-1 production by human synovial fibroblasts in vitro

✍ Scribed by Carrie Langdon; Jonathon Leith; Carl D. Richards; Frank Smith


Publisher
John Wiley and Sons
Year
1997
Tongue
English
Weight
766 KB
Volume
40
Category
Article
ISSN
0004-3591

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✦ Synopsis


To measure levels of oncostatin M (OSM) in the synovial fluid of rheumatoid arthritis (FU) patients and to examine the activities of human OSM in the regulation of human synovial fibroblast (HSF) production of chemokines and matrix metalloproteinases (MMP-1 and MMP-3) in vitro.

Methods. We examined the levels of OSM in the synovial fluids of patients with arthritis by an enzymelinked immunosorbent assay (ELISA). ELISA of cell culture supernatants and Northern blots were used to assess responses of HSF to interleukin-la (IL-la), OSM, and other members of the IL-6/leukemia inhibitory factor (IL-6/LIF) family of cytokines.

Results. We detected variable levels of OSM antigen in 9 of 10 RA patient synovial fluids, but levels were not detectable in 9 of 10 osteoarthritis (OA) patient fluids. Upon examining the responses of HSF in culture, OSM stimulated monocyte chemoattractant protein 1 (MCP-l), whereas RANTES secretion (regulated upon activation, normal T expressed and presumably secreted) was not altered by OSM alone. In IL-lainduced cells, OSM costimulation further enhanced MCP-1 release, but inhibited the release of RANTES and IL-8. Other members of the IL-6/LIF family of cytokines did not show these effects. OSM induced a small elevation of MMP-1 production over 2 and 3 days of stimulation (2-fold), and acted significantly to enhance IL-la-induced production of MMP-1 (to 8-fold Supported by the Arthritis Society of Canada. Dr. Richards is the recipient of a Career Scientist award from the Ontario Ministry of Health.


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