Division of Cellular Biology, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92037, USA.
Immunology. 2012 Sep;137(1):1-19. doi: 10.1111/j.1365-2567.2012.03591.x.
More than half of the known protein tyrosine phosphatases (PTPs) in the human genome are expressed in T cells, and significant progress has been made in elucidating the biology of these enzymes in T-cell development and function. Here we provide a systematic review of the current understanding of the roles of PTPs in T-cell activation, providing insight into their mechanisms of action and regulation in T-cell receptor signalling, the phenotypes of their genetically modified mice, and their possible involvement in T-cell-mediated autoimmune disease. Our projection is that the interest in PTPs as mediators of T-cell homeostasis will continue to rise with further functional analysis of these proteins, and PTPs will be increasingly considered as targets of immunomodulatory therapies.
人类基因组中已知的蛋白酪氨酸磷酸酶 (PTPs) 有一半以上在 T 细胞中表达,在阐明这些酶在 T 细胞发育和功能中的生物学作用方面已经取得了重大进展。在这里,我们对 PTPs 在 T 细胞激活中的作用的现有认识进行了系统回顾,深入了解了它们在 T 细胞受体信号转导中的作用机制和调节、其基因修饰小鼠的表型以及它们在 T 细胞介导的自身免疫性疾病中的可能参与。我们预计,随着对这些蛋白的进一步功能分析,人们对 PTPs 作为 T 细胞动态平衡介质的兴趣将继续增加,并且 PTPs 将越来越被视为免疫调节治疗的靶点。