Oncostatin M decreases interleukin-1 β secretion by human synovial fibroblasts and attenuates an acute inflammatory reaction in vivo.
Oncostatin M decreases interleukin-1 β secretion by human synovial fibroblasts and attenuates an acute inflammatory reaction in vivo.
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DOI:
10.1111/j.1582-4934.2011.01412.x
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发表时间:
2012-06
影响因子:
5.3
通讯作者:
Pouliot M
中科院分区:
文献类型:
--
作者:
Dumas A;Lagarde S;Laflamme C;Pouliot M
Oncostatin M (OSM) is a pleiotropic cytokine of the IL-6 family and displays both pro-inflammatory and anti-inflammatory activities. We studied the impact of OSM on the gene activation profile of human synovial cells, which play a central role in the progression of inflammatory responses in joints. In synovial cells stimulated with lipopolysaccharide and recombinant human granulocyte-macrophage colony-stimulating factor, recombinant human OSM and native OSM secreted by human granulocytes both reduced the gene expression and secretion of IL-1β and CXCL8, but increased that of IL-6 and CCL2. This impact on synovial cell activation was not obtained using IL-6 or leukaemia inhibitory factor. Signal transducer and activator of transcription-1 appeared to mediate the effects of OSM on stimulated human synovial fibroblasts. In the murine dorsal air pouch model of inflammation, OSM reduced the expression of the pro-inflammatory cytokines IL-1β and TNF-α in lining tissues, and their presence in the cavity. These results as a whole suggest an anti-inflammatory role for OSM, guiding inflammatory processes towards resolution.
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影响因子:
4
作者:
Cadieux, JS;Leclerc, P;Pouliot, M
通讯作者:
Pouliot, M
影响因子:
5.5
作者:
Goldring, SR
通讯作者:
Goldring, SR
影响因子:
27.4
作者:
Buckley, CD;Filer, A;Salmon, M
通讯作者:
Salmon, M
影响因子:
6.4
作者:
Dussault, AA;Pouliot, M
通讯作者:
Pouliot, M
影响因子:
7.3
作者:
EDWARDS, JCW;SEDGWICK, AD;WILLOUGHBY, DA
通讯作者:
WILLOUGHBY, DA