Induction of COX-2 expression by nitric oxide in rheumatoid synovial cells

被引:30
作者
Honda, S
Migita, K
Hirai, Y
Ueki, Y
Yamasaki, S
Urayama, S
Kawabe, Y
Fukuda, T
Kawakami, A
Kamachi, M
Kita, M
Ida, H
Aoyagi, T
Eguchi, K
机构
[1] Nagasaki Univ, Sch Med, Dept Internal Med 1, Nagasaki 8528501, Japan
[2] Kurume Univ, Sch Med, Dept Internal Med 1, Kurume, Fukuoka, Japan
关键词
D O I
10.1006/bbrc.2000.2228
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
Prostaglandins formed by cyclooxygenase (COX) enzymes are important mediators of inflammation. The contribution of inducible COX-2 in the rheumatoid synovium is well documented. In this study, we evaluated the contribution of nitric oxide (NO) to COX-2 expression in rheumatoid synovial cells. Exposure of rheumatoid synovial cells to a NO donor, SNAP, induced COX-2 protein expression in a dose-dependent manner. RT-PCR analysis also demonstrated that COX-2 mRNA was induced in SNAP-treated synovial cells. Dexamethasone at therapeutic concentrations markedly inhibited this NO-mediated COX-2 expression in synovial cells. In contrast to its effect on COX-2 expression, SNAP did not affect the constitutive expression of COX-1 in rheumatoid synovial cells. Our findings suggest that NO is an important modulator of COX-2 expression and that glucocorticoids exert their anti-inflammatory action in rheumatoid synovium, at least in part, by suppression of COX-2 induction. (C) 2000 Academic Press.
引用
收藏
页码:928 / 931
页数:4
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