Klann Jane E, Remedios Kelly A, Kim Stephanie H, Metz Patrick J, Lopez Justine, Mack Lauren A, Zheng Ye, Ginsberg Mark H, Petrich Brian G, Chang John T
Department of Medicine, University of California San Diego, La Jolla, CA 92093.
Nomis Foundation Laboratories for Immunobiology and Microbial Pathogenesis, Salk Institute for Biological Studies, La Jolla, CA 92037; and.
J Immunol. 2017 Jun 15;198(12):4639-4651. doi: 10.4049/jimmunol.1601165. Epub 2017 May 17.
Talin, a cytoskeletal protein essential in mediating integrin activation, has been previously shown to be involved in the regulation of T cell proliferation and function. In this study, we describe a role for talin in maintaining the homeostasis and survival of the regulatory T (Treg) cell pool. T cell-specific deletion of talin in mice resulted in spontaneous lymphocyte activation, primarily due to numerical and functional deficiencies of Treg cells in the periphery. Peripheral talin-deficient Treg cells were unable to maintain high expression of IL-2Rα, resulting in impaired IL-2 signaling and ultimately leading to increased apoptosis through downregulation of prosurvival proteins Bcl-2 and Mcl-1. The requirement for talin in maintaining high IL-2Rα expression by Treg cells was due, in part, to integrin LFA-1-mediated interactions between Treg cells and dendritic cells. Collectively, our data suggest a critical role for talin in Treg cell-mediated maintenance of immune homeostasis.
踝蛋白是一种在介导整合素激活过程中必不可少的细胞骨架蛋白,先前已证明它参与调节T细胞增殖和功能。在本研究中,我们描述了踝蛋白在维持调节性T(Treg)细胞库的稳态和存活中的作用。小鼠中T细胞特异性缺失踝蛋白导致淋巴细胞自发激活,主要是由于外周Treg细胞在数量和功能上的缺陷。外周缺乏踝蛋白的Treg细胞无法维持IL-2Rα的高表达,导致IL-2信号传导受损,并最终通过下调促生存蛋白Bcl-2和Mcl-1导致细胞凋亡增加。Treg细胞维持高IL-2Rα表达对踝蛋白的需求部分归因于整合素LFA-1介导的Treg细胞与树突状细胞之间的相互作用。总体而言,我们的数据表明踝蛋白在Treg细胞介导的免疫稳态维持中起关键作用。