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Signal transduction pathways involving p38 MAPK, JNK, NFkB and AP-1 influences the response of chondrocytes cultured in agarose constructs to IL-1b and dynamic compression

By T.T. Chowdhury, D. Salter, D.L. Bader and D.A. Lee

Abstract

Objective and Design: to examine whether inhibitors of the MAPK pathways will influence the response of bovine chondrocytes cultured in agarose constructs to IL-1? and dynamic compression.<br/><br/>Methods: dose-response studies were conducted under IL-1? conditions with either SB203580, SP600125, PDTC or curcumin. In separate experiments, constructs were treated with IL-1? and an appropriate concentration of inhibitor and subjected to 15% dynamic compression. Nitrite and PGE2 release, 35SO4 and [3H]-thymidine incorporation were subsequently measured using biochemical assays.<br/><br/>Results: all inhibitors reduced the IL-1? induced nitrite and PGE2 release in a dose-dependent manner. The inhibition of [3H]-thymidine incorporation by IL-1? was partially reversed with SB203580, SP600125 or curcumin, but not PDTC. In most cases, the inhibitors reduced 35SO4 incorporation with IL-1?. For the mechanical loading studies, the inhibitors reduced the compression-induced inhibition of nitrite and PGE2 release and restored [3H]-thymidine and 35SO4 incorporation.<br/><br/>Conclusions: the MAPK, AP-1 and NF-?B signalling pathways are involved in the upregulation of NO and PGE2 release by IL-1?. Dynamic compression stimulates cell proliferation and proteoglycan synthesis in the presence of IL-1? and/or inhibitors of the MAPKs and NF?B and AP-1 signalling pathways. This experimental approach could provide valuable information for the biophysical/pharmacological treatment of O

Topics: R1
Year: 2008
OAI identifier: oai:eprints.soton.ac.uk:189301
Provided by: e-Prints Soton
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