Regulation of T cell integrin function by adapter proteins

被引:0
|
作者
Rebecca G. Baker
Gary A. Koretzky
机构
[1] University of Pennsylvania School of Medicine,Leonard and Madlyn Abramson Family Cancer Research Institute
[2] University of Pennsylvania School of Medicine,Department of Pathology and Laboratory Medicine
[3] University of Pennsylvania School of Medicine,Department of Medicine
来源
Immunologic Research | 2008年 / 42卷
关键词
T lymphocyte; Signaling; Integrins; Adapters;
D O I
暂无
中图分类号
学科分类号
摘要
Integrins are cell surface heterodimers that bind adhesion molecules expressed on other cells or in the extracellular matrix. Integrin-mediated interactions are critical for T cell development in the thymus, migration of T cells in the periphery, and induction of T cell effector functions. In resting T cells, integrins are maintained in a low affinity state. Engagement of the T cell receptor or chemokine receptors increases integrin affinity, enabling integrins to bind their ligands and initiate a signaling cascade resulting in altered cell morphology and motility. Our laboratory is interested how adapter proteins, mediators of intracellular signal transduction, regulate both signals from the T cell receptor to integrins (inside-out signaling) and (outside-in) signals from integrins into the cell.
引用
收藏
页码:132 / 144
页数:12
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