Bradykinin induces a vapid cyclooxygenase-2 mRNA expression via Ca2+ mobilization in human gingival fibroblasts primed with interleukin-1β

被引:17
作者
Nakao, S
Ogata, Y
Modéer, T
Segawa, N
Furuyama, S
Sugiya, H [1 ]
机构
[1] Nihon Univ, Dept Physiol, Sch Dent, Chiba 2718587, Japan
[2] Nihon Univ, Dept Periodontol, Sch Dent, Chiba 2718587, Japan
[3] Nihon Univ, Dept Pharmacol, Sch Dent, Chiba 2718587, Japan
[4] Karolinska Inst, Dept Pediat Dent, S-14104 Huddinge, Sweden
基金
日本学术振兴会;
关键词
D O I
10.1054/ceca.2001.0206
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We have previously demonstrated that bradykinin potentiates prostaglandin E, release in human gingival fibroblasts pretreated with interleukin-1 beta (priming), In this study, we demonstrate a potentiating effect of bradykinin on cyclooxygenase-2 mRNA expression in the interleukin-1 beta -primed fibroblasts. Interleukin-1 beta (200pg/ml) induced cyclooxygenase-2 mRNA expression, but not bradykinin (1 CIM). However, bradykinin rapidly and markedly increased the cyclooxygenase-2 mRNA expression in the fibroblasts primed with interleukin-1 beta. In the primed fibroblasts, ionomycin and thapsigargin mimicked the potentiating effect of bradykinin on the cyclooxygenase-2 mRNA expression. Dexamethasone and actinomycin D completely suppressed not only the interleukin-1 beta -induced cyclooxygenase-2 mRNA expression, but also the bradykinin-induced cyclooxygenase-2 mRNA expression in the interleukin-1 beta -primed fibroblasts, although cycloheximide did not inhibit the effects of interleukin-1 beta and bradykinin. These results suggest that bradykinin-induced prostaglandin E, synthesis is regulated at the level of the transcription of cyclooxygenase-2 mRNA via Ca2+ mobilization in the interleukin-1 beta -primed human gingival fibroblasts. (C) 2001 Harcourt Publishers Ltd.
引用
收藏
页码:446 / 452
页数:7
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