Signal transduction events regulating integrin function and T cell migration - New functions and complexity

被引:13
作者
Pribila, JT [1 ]
Shimizu, Y [1 ]
机构
[1] Univ Minnesota, Sch Med, Canc Ctr,Ctr Immunol, Dept Lab Med & Pathol, Minneapolis, MN 55455 USA
关键词
T lymphocyte; integrin; signal transduction; chemokine; adhesion; migration;
D O I
10.1385/IR:27:1:107
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Integrin receptors facilitate T cell function by mediating adhesive events critical for T cell trafficking and recognition of foreign antigen, including interactions with vascular endothelium, extracellular matrix components, and antigen-presenting cells. Consequently, the functional activity of integrin receptors is acutely regulated by various intracellular signals delivered by other cell surface receptors, resulting in rapid changes in T cell adhesion and migration. This review highlights recent insights into our understanding of the signaling events by which the CD3/T cell receptor complex and chemokine receptors regulate integrin function and T cell migration. These studies highlight novel functions for several signaling molecules, including the tyrosine kinases Itk and ZAP-70, and the adapter protein SLAP-130/Fyb. In addition, analysis of the regulation of integrin function and chemokine-mediated migration has highlighted the critical role that spatial localization of signaling molecules plays in signal transduction, and the importance of the actin cytoskeleton in T cell function.
引用
收藏
页码:107 / 128
页数:22
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