Novel mode of action of iloprost: in vitro downregulation of endothelial cell adhesion molecules

被引:55
作者
Della Bella, S [1 ]
Molteni, M [1 ]
Mocellin, C [1 ]
Fumagalli, S [1 ]
Bonara, P [1 ]
Scorza, R [1 ]
机构
[1] Univ Milan, Dept Internal Med, IRCCS, Osped Maggiore, Milan, Italy
来源
PROSTAGLANDINS & OTHER LIPID MEDIATORS | 2001年 / 65卷 / 2-3期
关键词
iloprost; HUVEC; lymphocytes; adhesion molecules; interleukin-1; systemic sclerosis;
D O I
10.1016/S0090-6980(01)00131-9
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
Iloprost is a stable prostacyclin analog commonly employed in the treatment of peripheral vascular disease and also indicated in the treatment of patients affected by systemic sclerosis (SSc) in the presence of severe Raynaud's phenomenon (RP). Several mechanisms of action of the drug other than vasodilation and antiplatelet effect have been demonstrated that may be involved in the exertion of its clinical efficacy. Aim of the present study was to investigate whether iloprost down-regulated lymphocyte adhesion to endothelium through a modulation of adhesion molecule expression on the surface of endothelial cells. In the presence of iloprost, both lymphocyte adhesion and IL-1 stimulated expression of ICAM-1 and ELAM-1 exhibited a significant reduction, while unstimulated adhesion molecule expression was not significantly affected. Our results confirm that iloprost is able to down-regulate lymphocyte adhesion to endothelial cells and indicate that endothelium itself could be target of iloprost administration. Attenuation of the inflammatory response through modulation of cellular interactions could be suggested as a potential mechanism of action of iloprost, when used in the treatment of pathological conditions characterized by endothelial activation. (C) 2001 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:73 / 83
页数:11
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