Cell Signaling and Immunity Section, Laboratory of Immune System Biology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA; Department of Pathology, University of Cambridge, Tennis Court Road, Cambridge CB2 1QP, UK; Section of Experimental and Translational Immunology, Department of Health Technology, Technical University of Denmark, 2800 Kongens Lyngby, Denmark.
Cell Signaling and Immunity Section, Laboratory of Immune System Biology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
Trends Immunol. 2023 Nov;44(11):917-931. doi: 10.1016/j.it.2023.09.002. Epub 2023 Oct 18.
Following stimulation, the T cell receptor (TCR) and its coreceptors integrate multiple intracellular signals to initiate T cell proliferation, migration, gene expression, and metabolism. Among these signaling molecules are the small GTPases RAS and RAP1, which induce MAPK pathways and cellular adhesion to activate downstream effector functions. Although many studies have helped to elucidate the signaling intermediates that mediate T cell activation, the molecules and pathways that keep naive T cells in check are less understood. Several recent studies provide evidence that RASA2 and RASA3, which are GAP1-family GTPase-activating proteins (GAPs) that inactivate RAS and RAP1, respectively, are crucial molecules that limit T cell activation and adhesion. In this review we describe recent data on the roles of RASA2 and RASA3 as gatekeepers of T cell activation and migration.
刺激后,T 细胞受体 (TCR) 和其辅助受体整合多种细胞内信号以启动 T 细胞增殖、迁移、基因表达和代谢。在这些信号分子中,小 GTPases RAS 和 RAP1 诱导 MAPK 途径和细胞黏附,从而激活下游效应功能。尽管许多研究有助于阐明介导 T 细胞激活的信号转导介质,但维持初始 T 细胞的分子和途径仍知之甚少。最近的几项研究提供了证据,表明分别使 RAS 和 RAP1 失活的 GAP1 家族 GTP 酶激活蛋白 (GAP) RASA2 和 RASA3 是限制 T 细胞激活和黏附的关键分子。在这篇综述中,我们描述了最近关于 RASA2 和 RASA3 作为 T 细胞激活和迁移的“守门员”的作用的数据。