Induction of cyclooxygenase-2 and enhanced release of prostaglandin E2 and I2 in human endothelial cells by engagement of CD40

被引:14
|
作者
Garlichs, CD [1 ]
Geis, T
Goppelt-Struebe, M
Eskafi, S
Schmidt, A
Schulze-Koops, H
Ludwig, J
Daniel, WG
Schmeisser, A
机构
[1] Univ Erlangen Nurnberg, Med Clin 2, Erlangen, Germany
[2] Univ Erlangen Nurnberg, Med Clin 4, Erlangen, Germany
[3] Univ Erlangen Nurnberg, Med Clin 3, Erlangen, Germany
关键词
cell culture; endothelial factors; immunology; inflammation;
D O I
10.1016/S0021-9150(01)00695-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: The hypothesis was tested that CD40-CD154 interaction is involved in the induction of cyclooxygenase-2 and the release of prostanoids in human endothelial cells. Methods and results: In a coculture model of human endothelial cells and a transfected CD 154 positive cell line, engagement of CD40 on endothelial cells dramatically increased the synthesis of prostacyclin, prostaglandin E, and thromboxane A(2). This upregulation was mediated through an induction of cyclooxygenase-2 (Cox-2), as it was blocked by Cox-2-selective inhibitors. Western blot analysis demonstrated that Cox-2 protein was markedly increased in endothelial cells following CD40 engagement, an effect that was inhibited by pretreatment of cells with an anti-CD154 antibody. Conclusion: The data indicate that signaling via CD40 constitutes a major pathway in human endothelial cells for the induction of Cox-2 and release of prostanoids. The CD40-Cox-2 axis thus may represent an important pathway for initiating or maintaining an inflammatory process at the vessel wall. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:9 / 16
页数:8
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