P-Selectin Antagonism in Inflammatory Disease

被引:18
作者
Woollard, Kevin J. [1 ]
Chin-Dusting, Jaye [1 ]
机构
[1] Baker IDI Heart & Diabet Inst, Melbourne, Vic 3004, Australia
基金
英国医学研究理事会;
关键词
P-selectin; inflammation; atherosclerosis; leukocyte; endothelium; cellular adhesion; GLYCOPROTEIN LIGAND-IMMUNOGLOBULIN; INTERCELLULAR-ADHESION MOLECULE-1; ISCHEMIA-REPERFUSION INJURY; ANTI-E-SELECTIN; CELL-ADHESION; NEOINTIMAL FORMATION; MONOCLONAL-ANTIBODY; LEUKOCYTE ADHESION; IN-VITRO; ATHEROSCLEROTIC PLAQUES;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Inflammation plays a fundamental role in many chronic diseases, including atherosclerosis associated cardiovascular disease. Adhesion of immune cells plays a critical role in the inflammatory response and indeed the pathophysiology of inflammatory related diseases. P-selectin is an inflammatory adhesion molecule, enabling the recruitment of leukocytes to the endothelium and to activated platelets involved in the growing thrombus. P-selectin is critical in the progression of atherosclerosis as evidenced by knockout animal models where P-selectin knockout mice crossed with apoE deficient mice exhibit significantly reduced atherosclerosis and leukocyte recruitment in the plaque. A soluble form of P-selectin also exists, which may have pro-atherogenic and pro-thrombotic effects. Thus targeting of P-selectin remains a strong clinical candidate for developing novel therapeutic strategies in inflammatory diseases. This review will discuss the role of P-selectin and describe the function of P-selectin antagonists as clinical targets.
引用
收藏
页码:4113 / 4118
页数:6
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