Kirchhof Mark G, Chau Luan A, Lemke Caitlin D, Vardhana Santosh, Darlington Peter J, Márquez Maria E, Taylor Roy, Rizkalla Kamilia, Blanca Isaac, Dustin Michael L, Madrenas Joaquín
FOCIS Centre for Clinical Immunology and Immunotherapeutics, Robarts Research Institute, and Department of Microbiology and Immunology, University of Western Ontario, London, Ontario, Canada.
J Immunol. 2008 Aug 1;181(3):1927-36. doi: 10.4049/jimmunol.181.3.1927.
T cell activation through the Ag receptor (TCR) requires sustained signaling from signalosomes within lipid raft microdomains in the plasma membrane. In a proteomic analysis of lipid rafts from human T cells, we identified stomatin-like protein (SLP)-2 as a candidate molecule involved in T cell activation through the Ag receptor. In this study, we show that SLP-2 expression in human primary lymphocytes is up-regulated following in vivo and ex vivo activation. In activated T cells, SLP-2 interacts with components of TCR signalosomes and with polymerized actin. More importantly, up-regulation of SLP-2 expression in human T cell lines and primary peripheral blood T cells increases effector responses, whereas down-regulation of SLP-2 expression correlates with loss of sustained TCR signaling and decreased T cell activation. Our data suggest that SLP-2 is an important player in T cell activation by ensuring sustained TCR signaling, which is required for full effector T cell differentiation, and point to SLP-2 as a potential target for immunomodulation.
通过抗原受体(TCR)激活T细胞需要来自质膜脂筏微结构域内信号小体的持续信号传导。在对人T细胞脂筏的蛋白质组学分析中,我们鉴定出类stomatin蛋白(SLP)-2是一种通过抗原受体参与T细胞激活的候选分子。在本研究中,我们表明,体内和体外激活后人原代淋巴细胞中SLP-2的表达上调。在活化的T细胞中,SLP-2与TCR信号小体的成分以及聚合肌动蛋白相互作用。更重要的是,人T细胞系和原代外周血T细胞中SLP-2表达的上调增加效应反应,而SLP-2表达的下调与持续TCR信号传导的丧失和T细胞活化的降低相关。我们的数据表明,SLP-2通过确保持续的TCR信号传导在T细胞激活中起重要作用,这是效应T细胞完全分化所必需的,并指出SLP-2作为免疫调节的潜在靶点。