Involvement of p38 mitogen-activated protein kinase in lipopolysaccharide-induced iNOS and COX-2 expression in J774 macrophages

被引:210
作者
Chen, BC
Chen, YH
Lin, WW [1 ]
机构
[1] Natl Taiwan Univ, Coll Med, Dept Pharmacol, Taipei, Taiwan
[2] Natl Taiwan Univ, Coll Med, Sch Pharm, Taipei, Taiwan
关键词
D O I
10.1046/j.1365-2567.1999.00747.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Both the nitrite and prostaglandin E-2 (PGE(2)) release caused by lipopolysaccharide (LPS) in J774 macrophages are inhibited by SE 203580, a specific p38 mitogen-activated protein kinase (MAPK) inhibitor, in a concentration-dependent manner. The 50% inhibitory concentration (IC50) for nitrite and PGE(2) responses was 1 mu M and 0.5 mu M, respectively. Inhibition was marked following simultaneous treatment with SE 203580 and LPS, and was much reduced when SE 203580 was added 6 hr after LPS treatment. In parallel, LPS induction of inducible NO synthase (iNOS) and cyclo-oxygenase-2 (COX-2) proteins and their steady-state levels of mRNA were reduced by SB 203580. LPS activation of nuclear factor-kappa B (NF-kappa B), activator protein-1 (AP-1) and p38 MAPK was also inhibited by SB 203580. These results suggest a crucial role of p38 MAPK in regulation of the transcriptional level of endotoxin LPS-induced iNOS and COX-2 protein expression.
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页码:124 / 129
页数:6
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