Kaitao Li, William Rittase, Zhou Yuan, Cheng Zhu
Wallace H. Coulter Department of Biomedical Engineering.
Institute for Bioengineering and Biosciences, Georgia Institute of Technology, Atlanta, GA 30332.
Curr Opin Biomed Eng. 2019 Dec;12:102-110. doi: 10.1016/j.cobme.2019.10.005. Epub 2019 Nov 1.
T-cell activation is the central event governing its development, differentiation, and effector functions. T-cell activation is initiated by the direct physical interaction of the T cell antigen receptor (TCR) with cognate peptide presented by the major histocompatibility complex (pMHC) molecule expressed on the antigen presenting cell (APC) surface. Since the identification of TCR as the only receptor for antigen on T cells three decades ago, studies have elucidated the major molecular players and signaling events responding to TCR stimulation. However, the question of how the physical event of pMHC binding is converted across the membrane into chemical events to initiate signal transduction remains elusive. Here we review recent investigations of T-cell activation using single-molecule force and fluorescence techniques that shed new light on this key question.
T细胞活化是控制其发育、分化和效应功能的核心事件。T细胞活化由T细胞抗原受体(TCR)与抗原呈递细胞(APC)表面表达的主要组织相容性复合体(pMHC)分子呈递的同源肽直接物理相互作用引发。自从三十年前将TCR鉴定为T细胞上唯一的抗原受体以来,研究已经阐明了响应TCR刺激的主要分子参与者和信号事件。然而,pMHC结合的物理事件如何跨膜转化为化学事件以启动信号转导的问题仍然难以捉摸。在这里,我们回顾了最近使用单分子力和荧光技术对T细胞活化的研究,这些研究为这个关键问题提供了新的线索。