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T细胞受体介导的调控T细胞发育的迹象和信号。

T cell receptor-mediated signs and signals governing T cell development.

作者信息

van Oers N S

机构信息

Center for Immunology and the Department of Microbiology, UT Southwestern Medical Center, Room NA7.201, 6000 Harry Hines Blvd., Dallas, TX 75235-9093, USA.

出版信息

Semin Immunol. 1999 Aug;11(4):227-37. doi: 10.1006/smim.1999.0179.

Abstract

The developmental fate of T cells is largely controlled by the nature and success of signals mediated by the pre-T cell receptor (TCR) and TCR complexes. These intracellular signals are regulated by cascades of protein tyrosine phosphorylations initiated following ligand binding to the pre-TCR or TCR complexes. The phosphorylation cascades are primarily orchestrated by two distinct families of protein tyrosine kinases (PTKs), the Src- and the Syk/ZAP-70-families. Germline gene targeting experiments, several human immunodeficiencies, and somatic cell mutants have all contributed to our understanding of how these families of kinases coordinate their actions to promote signaling. Upon activation, the PTKs transmit their signals to a number of newly described adaptor proteins including LAT, SLP-76, and vav, among others. The following review combines results derived from different experimental strategies to examine the contributions of the PTKs and the adaptor molecules to pre-TCR and TCR signaling processes.

摘要

T细胞的发育命运很大程度上受前T细胞受体(TCR)和TCR复合物介导的信号的性质和成功与否的控制。这些细胞内信号由配体与前TCR或TCR复合物结合后引发的蛋白质酪氨酸磷酸化级联反应调节。磷酸化级联反应主要由两个不同的蛋白质酪氨酸激酶(PTK)家族协调,即Src家族和Syk/ZAP-70家族。种系基因靶向实验、几种人类免疫缺陷疾病以及体细胞突变体都有助于我们理解这些激酶家族如何协调其作用以促进信号传导。激活后,PTK将其信号传递给许多新发现的衔接蛋白,包括LAT、SLP-76和vav等。以下综述结合了来自不同实验策略的结果,以研究PTK和衔接分子对前TCR和TCR信号传导过程的作用。

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