Samelson Lawrence E
Laboratory of Cellular and Molecular Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, 37 Convent Drive, Building 37, Room 1E24, Bethesda, Maryland, 20892-4255, USA.
Annu Rev Immunol. 2002;20:371-94. doi: 10.1146/annurev.immunol.20.092601.111357. Epub 2001 Oct 4.
Engagement of the T cell antigen receptor (TCR) leads to a complex series of molecular changes at the plasma membrane, in the cytoplasm, and at the nucleus that lead ultimately to T cell effector function. Activation at the TCR of a set of protein tyrosine kinases (PTKs) is an early event in this process. This chapter reviews some of the critical substrates of these PTKs, the adapter proteins that, following phosphorylation on tyrosine residues, serve as binding sites for many of the critical effector enzymes and other adapter proteins required for T cell activation. The role of these adapters in binding various proteins, the interaction of adapters with plasma membrane microdomains, and the function of adapter proteins in control of the cytoskeleton are discussed.
T细胞抗原受体(TCR)的激活会导致质膜、细胞质和细胞核发生一系列复杂的分子变化,最终导致T细胞效应功能的产生。一组蛋白酪氨酸激酶(PTK)在TCR处的激活是这一过程中的早期事件。本章回顾了这些PTK的一些关键底物,即衔接蛋白,它们在酪氨酸残基磷酸化后,作为许多T细胞激活所需的关键效应酶和其他衔接蛋白的结合位点。讨论了这些衔接蛋白在结合各种蛋白质中的作用、衔接蛋白与质膜微结构域的相互作用以及衔接蛋白在控制细胞骨架中的功能。