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衔接蛋白对T细胞整合素功能的调控。

Regulation of T cell integrin function by adapter proteins.

作者信息

Baker Rebecca G, Koretzky Gary A

机构信息

Leonard and Madlyn Abramson Family Cancer Research Institute, University of Pennsylvania School of Medicine, Philadelphia, PA, 19104, USA.

出版信息

Immunol Res. 2008;42(1-3):132-44. doi: 10.1007/s12026-008-8047-8.

Abstract

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.

摘要

整合素是细胞表面的异二聚体,可与其他细胞上或细胞外基质中表达的黏附分子结合。整合素介导的相互作用对于胸腺中T细胞的发育、外周T细胞的迁移以及T细胞效应功能的诱导至关重要。在静息T细胞中,整合素维持在低亲和力状态。T细胞受体或趋化因子受体的激活会增加整合素的亲和力,使整合素能够结合其配体并启动信号级联反应,从而导致细胞形态和运动性的改变。我们实验室感兴趣的是衔接蛋白(细胞内信号转导的介质)如何调节从T细胞受体到整合素的信号(由内向外信号传导)以及从整合素到细胞内的(由外向内)信号。

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