Integrins: dynamic scaffolds for adhesion and signaling in platelets

被引:421
|
作者
Shattil, SJ
Newman, PJ
机构
[1] Scripps Res Inst, Dept Cell Biol, La Jolla, CA USA
[2] Scripps Res Inst, Dept Mol, La Jolla, CA USA
[3] Scripps Res Inst, Dept Expt Med, La Jolla, CA USA
[4] Blood Ctr SE Wisconsin Inc, Blood Res Inst, Milwaukee, WI USA
关键词
D O I
10.1182/blood-2004-04-1257
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The major platelet integrin, alphaIIbbeta3, is required for platelet interactions with proteins in plasma and the extracellular matrices (ECMs) that are essential for platelet adhesion and aggregation during hemostasis and arterial thrombosis. Ligand binding to alphaIIbbeta3 is controlled by inside-out signals that modulate receptor conformation and clustering. In turn, ligand binding triggers outside-in signals through aIIbbeta3 that, when disrupted, can cause a bleeding diathesis. In the past 5 years there has been an explosion of knowledge about the structure and function of aIIbeta3 and the related integrin, alphaVbeta3. These developments are discussed here, and current models of bidirectional aIIbbeta3 signaling are presented as frameworks for future investigations. An understanding that alphaIIbbeta3 functions as a dynamic molecular scaffold for extracellular and intracellular proteins has translated into diagnostic and therapeutic insights relevant to hematology and cardiovascular medicine, and further advances can be anticipated.(C) 2004 by The American Society of Hematology.
引用
收藏
页码:1606 / 1615
页数:10
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