Department of Molecular Medicine, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.
Armauer Hansen Research Institute, Addis Abeba, Ethiopia.
Sci Rep. 2018 Sep 6;8(1):13319. doi: 10.1038/s41598-018-31510-6.
Polarization of T cells towards the antigen presenting cell (APC) is critically important for appropriate activation and differentiation of the naïve T cell. Here we used imaging flow cytometry (IFC) and show that the activation induced Lck and Itk adapter T cell specific adapter protein (TSAd), encoded by SH2D2A, modulates polarization of T cells towards the APC. Upon exposure to APC presenting the cognate antigen Id, Sh2d2a-/- CD4+ T cells expressing Id-specific transgenic T cell receptor (TCR), displayed impaired polarization of F-actin and TCR to the immunological synapse (IS). Sh2d2a-/- T-cells that did polarize F-actin and TCR still displayed impaired polarization of PKCξ, PAR3 and the microtubule-organizing center (MTOC). In vitro differentiation of activated Sh2d2a-/- T cells was skewed towards an effector memory (Tem) rather than a central memory (Tcm) phenotype. A similar trend was observed for Id-specific TCR Sh2d2a-/- T cells stimulated with APC and cognate antigen. Taken together our data suggest that TSAd modulates differentiation of experienced T cells possibly through polarization of CD4+ T cells towards the APC.
T 细胞向抗原呈递细胞 (APC) 的极化对于初始 T 细胞的适当激活和分化至关重要。在这里,我们使用成像流式细胞术 (IFC) 并表明,由 SH2D2A 编码的激活诱导的 Lck 和 Itk 衔接子 T 细胞特异性衔接蛋白 (TSAd) 调节 T 细胞向 APC 的极化。在暴露于呈递同源抗原 Id 的 APC 后,表达 Id 特异性转基因 T 细胞受体 (TCR) 的 Sh2d2a-/- CD4+ T 细胞显示出 F-肌动蛋白和 TCR 向免疫突触 (IS) 的极化受损。虽然 Sh2d2a-/- T 细胞确实极化了 F-肌动蛋白和 TCR,但它们仍然显示出 PKCξ、PAR3 和微管组织中心 (MTOC) 的极化受损。体外激活的 Sh2d2a-/- T 细胞的分化偏向于效应记忆 (Tem) 而不是中央记忆 (Tcm) 表型。用 APC 和同源抗原刺激的 Id 特异性 TCR Sh2d2a-/- T 细胞也观察到类似的趋势。总之,我们的数据表明,TSAd 通过将 CD4+ T 细胞极化向 APC 来调节经验丰富的 T 细胞的分化。