The dialogue between endothelial cells and monocytes/macrophages in vascular syndromes

被引:45
|
作者
Martin, J.
Collot-Teixeira, S.
McGregor, L.
McGregor, J. L.
机构
[1] Thrombosis Res Inst, Genom & Atherothrombosis Lab, London SW3 6LR, England
[2] Fac Med RTH Laennec, INSERM, EA3740, IFR62, Lyon, France
[3] Univ London, Univ London Kings Coll, Div Cardiovasc, London WC1E 7HU, England
[4] INSERM, U689, F-75730 Paris, France
关键词
inflammation; endothelial cells; monocytes/macrophages; cell adhesion molecules; chemokines; polymorphisms; genomic tools;
D O I
10.2174/138161207780831248
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The aim of this chapter is to present and identify potential pharmacological targets in endothelial cell-monocyte interactions leading to vascular syndrome and involving inflammation, coagulation, vascular remodelling and thrombosis. Increasing evidence is indicating that endothelial cells play a key role in atherothombosis by their capacity to attract, bind and allow the extravasation of monocytes to sites of inflammation. Surface expression and/or activation of constituent cell adhesion molecules (for e.g. P-selectin, E-selectin, ICAM-1, and VCAM-1) on endothelial cells together with chemokines such as CXCL8 (IL-8), Platelet-activating factor (PAF), CCL2 and CCL5 (Table 1) allow the rolling, adhesion and extravasation of monocytes. This review focuses on pharmacological targets implicated in endothelial cells interactions with monocytes/macrophages in vascular disease states and on cutting edge genomic tools for the identification and characterization of such targets.
引用
收藏
页码:1751 / 1759
页数:9
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