Cell Biology and Physiology Center, National Heart Lung and Blood Institute, National Institutes of Health, Bethesda, Maryland 20892, USA; email:
Annu Rev Immunol. 2019 Apr 26;37:201-224. doi: 10.1146/annurev-immunol-042718-041341. Epub 2018 Dec 21.
The engagement of a T cell with an antigen-presenting cell (APC) or activating surface results in the formation within the T cell of several distinct actin and actomyosin networks. These networks reside largely within a narrow zone immediately under the T cell's plasma membrane at its site of contact with the APC or activating surface, i.e., at the immunological synapse. Here we review the origin, organization, dynamics, and function of these synapse-associated actin and actomyosin networks. Importantly, recent insights into the nature of these actin-based cytoskeletal structures were made possible in several cases by advances in light microscopy.
T 细胞与抗原呈递细胞 (APC) 或激活表面的结合会导致 T 细胞内形成几个不同的肌动蛋白和肌球蛋白网络。这些网络主要存在于 T 细胞与 APC 或激活表面接触部位的质膜下方的一个狭窄区域内,即免疫突触处。在这里,我们综述了这些突触相关肌动蛋白和肌球蛋白网络的起源、组织、动态和功能。重要的是,在几种情况下,通过在光学显微镜方面的进展,使我们对这些基于肌动蛋白的细胞骨架结构的性质有了更深入的了解。