Regulation of interleukin-β-induced interleukin-6 gene expression in human fibroblast-like synoviocytes by p38 mitogen-activated protein kinase

被引:200
作者
Miyazawa, K
Mori, A
Miyata, H
Akahane, M
Ajisawa, Y
Okudaira, H
机构
[1] Kissei Pharmaceut Co Ltd, Cent Res Labs, Matsumoto, Nagano 3998304, Japan
[2] Natl Sagamihara Hosp, Clin Res Ctr Allergy & Rheumatol, Kanagawa 2888522, Japan
[3] Univ Tokyo, Fac Med, Dept Med & Phys Therapy, Tokyo 1130033, Japan
关键词
D O I
10.1074/jbc.273.38.24832
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Involvement of p38 mitogen-activated protein (MAP) kinase in interleukin (IL)-6 gene expression of human fibroblast-like synoviocytes (FLSs) was assessed. p38 MAP kinase was constitutively expressed in human FLSs and activated in response to IL-1 beta. A pyridinylimidazole compound, SB203580, inhibited p38 MAP kinase activity in vivo, since the activity of MAPKAP kinase-2 (a substrate of p38 MAP kinase) in IL-1 beta-stimulated FLSs was totally suppressed by it. SB203580 concentration-dependently inhibited protein production and gene expression of IL-6 by human FLSs. The effect of SB203580 was dependent on de novo protein synthesis. SB203580 significantly reduced the stability of IL-6 mRNA without affecting the rate of IL-6 gene transcription. Here, we provide evidence that p38 MAP kinase is activated in response to IL-1 beta in human FLSs and is involved in IL-6 synthesis by stabilizing IL-6 mRNA.
引用
收藏
页码:24832 / 24838
页数:7
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