Kaizuka Yoshihisa
National Institute for Materials Science, Tsukuba, Ibaraki 305-0047, Japan.
Membranes (Basel). 2020 Dec 19;10(12):443. doi: 10.3390/membranes10120443.
Among various types of membrane proteins that are regulated by cytoskeleton, the T cell receptor (TCR) greatly benefits from these cellular machineries for its function. The T cell is activated by the ligation of TCR to its target agonist peptide. However, the binding affinity of the two is not very strong, while the T cell needs to discriminate agonist from many nonagonist peptides. Moreover, the strength and duration of the activation signaling need to be tuned for immunological functions. Many years of investigations revealed that dynamic acto-myosin cytoskeletons and plasma membranes in T cells facilitate such regulations by modulating the spatiotemporal distributions of proteins in plasma membranes and by applying mechanical loads on proteins. In these processes, protein dynamics in multiple scales are involved, ranging from collective molecular motions and macroscopic molecular organizations at the cell-cell interface to microscopic changes in distances between receptor and ligand molecules. In this review, details of how cytoskeletons and membranes regulate these processes are discussed, with the emphasis on how all these processes are coordinated to occur within a single cell system.
在受细胞骨架调节的各类膜蛋白中,T细胞受体(TCR)的功能极大地受益于这些细胞机制。T细胞通过TCR与其靶激动剂肽的连接而被激活。然而,两者的结合亲和力并不很强,而T细胞需要从众多非激动剂肽中区分出激动剂。此外,激活信号的强度和持续时间需要针对免疫功能进行调节。多年的研究表明,T细胞中动态的肌动蛋白-肌球蛋白细胞骨架和质膜通过调节质膜中蛋白质的时空分布以及对蛋白质施加机械负荷来促进此类调节。在这些过程中,涉及多个尺度的蛋白质动态变化,从细胞-细胞界面的集体分子运动和宏观分子组织到受体与配体分子之间距离的微观变化。在本综述中,将讨论细胞骨架和膜如何调节这些过程的细节,重点是所有这些过程如何在单个细胞系统内协同发生。