Polarity of CD4+T cells towards the antigen presenting cell is regulated by the Lck adapter TSAd

被引:7
作者
Abrahamsen, Greger [1 ]
Sundvold-Gjerstad, Vibeke [1 ]
Habtamu, Meseret [1 ,2 ]
Bogen, Bjarne [3 ,4 ]
Spurkland, Anne [1 ]
机构
[1] Univ Oslo, Inst Basic Med Sci, Dept Mol Med, Oslo, Norway
[2] Armauer Hansen Res Inst, Addis Ababa, Ethiopia
[3] Oslo Univ Hosp, Rikshosp, Inst Immunol, Ctr Immune Regulat, Oslo, Norway
[4] Univ Oslo, KG Jebsen Ctr Influenza Res, Oslo, Norway
来源
SCIENTIFIC REPORTS | 2018年 / 8卷
关键词
CD4(+) T-CELLS; CYTOSKELETAL POLARIZATION; RECEPTOR SIGNALS; DENDRITIC CELLS; TUMOR-CELLS; ACTIVATION; PROTEIN; ACTIN; COMPLEX; SYNAPSE;
D O I
10.1038/s41598-018-31510-6
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Polarization of T cells towards the antigen presenting cell (APC) is critically important for appropriate activation and differentiation of the naive 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 PKC xi, 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.
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页数:13
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