T Cell Signalling Laboratory, Sir William Dunn School of Pathology University of Oxford, South Parks Road, Oxford OX1 3RE, U.K.
Essays Biochem. 2015;57:165-75. doi: 10.1042/bse0570165.
The organization of the T-cell's plasma membrane continues to nourish the curiosity of immunologists, cell biologists and biophysicists. The main reason is the biological and biomedical interest to understand the workings of the cell-cell communication network activated by T-cells during an immune response. The molecular armamentarium of the T-cell plasma membrane helps to identify with high sensitivity, specificity and rapidity antigens from invading microbial pathogens and prepare adequate countermeasures to fend them off, while protecting from attacks against our normal tissues. Many T-cell membrane proteins act as receptors to carry out and finely tune these complex tasks. However, the TCR (T-cell receptor) holds a decisive hegemony for its crucial contribution in steering T-cell function and fate. An emerging notion is that TCR proximal signalling occurs at submicrometre-scale membrane domains. In the present chapter, we discuss the current knowledge on the TCR structure and the associated signal transduction machinery and how the notion of membrane nanodomains has decisively contributed to further understand the molecular basis of T-cell activation.
T 细胞的质膜结构组织不断激发免疫学家、细胞生物学家和生物物理学家的好奇心。其主要原因是人们对细胞间通讯网络在免疫反应中被 T 细胞激活的工作原理有着浓厚的生物学和生物医学兴趣。T 细胞质膜的分子武器帮助 T 细胞以高灵敏度、特异性和快速性识别入侵的微生物病原体,并准备好充分的对策来抵御它们,同时防止对我们正常组织的攻击。许多 T 细胞膜蛋白作为受体发挥作用,以完成和精细调节这些复杂任务。然而,TCR(T 细胞受体)因其在指导 T 细胞功能和命运方面的关键作用而具有决定性的优势。一个新出现的观点是,TCR 近端信号发生在亚微米尺度的膜域。在本章中,我们讨论了 TCR 结构及其相关信号转导机制的最新知识,以及膜纳米域的概念如何为进一步理解 T 细胞激活的分子基础做出了决定性贡献。