New insights into the structural basis of integrin activation

被引:152
作者
Xiong, JP
Stehle, T
Goodman, SL
Arnaout, MA [1 ]
机构
[1] Massachusetts Gen Hosp East, Renal Unit, Struct Biol Program, Leukocyte Biol & Inflammat Program, Charlestown, MA 02129 USA
[2] Harvard Univ, Sch Med, Charlestown, MA 02129 USA
[3] Massachusetts Gen Hosp, Lab Dev Immunol, Boston, MA 02114 USA
[4] Harvard Univ, Sch Med, Boston, MA USA
[5] Merck KGaA, Dept Oncol Res, Darmstadt, Germany
关键词
D O I
10.1182/blood-2003-01-0334
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Integrins are cell adhesion receptors that communicate biochemical and mechanical signals in a bidirectional manner across the plasma membrane and thus influence most cellular functions. Intracellular signals switch integrins into a ligand-competent state as a result of elicited conformational changes in the integrin ectodomain. Binding of extracellular ligands induces, in turn, structural changes that convey distinct signals to the cell interior. The structural basis of this bidirectional signaling has been the focus of intensive study for the past 3 decades. In this perspective, we develop a new hypothesis for integrin activation based on recent crystallographic, electron microscopic, and biochemical studies. (C) 2003 by The American Society of Hematology.
引用
收藏
页码:1155 / 1159
页数:5
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