Imaging the T-cell receptor: new approaches, new insights

被引:4
作者
Rochussen, Adam M. [1 ]
Lippert, Anna H. [1 ]
Griffiths, Gillian M. [1 ]
机构
[1] Cambridge Inst Med Res, Keith Peters Bldg, Biomed Campus,Hills Rd, Cambridge CB2 0XY, England
基金
英国惠康基金;
关键词
SUPERRESOLUTION; NANOCLUSTERS; MICROSCOPY; INITIATION; PROTEINS;
D O I
10.1016/j.coi.2023.102309
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
T cells recognize pathogenic antigens via the T-cell antigen receptor (TCR). This protein complex binds to antigen fragments on the surface of antigen-presenting cells. To understand how cellular activation can ensue rapidly from molecular recognition, the localization and distribution of the TCR on the surface of the resting T cell are of particular importance. Conflicting results regarding TCR distribution have emerged from recent studies using a range of imaging techniques, including total internal reflection and single-molecule localization microscopy modalities. Here, we review the differing results and the potential biases inherent in differing imaging approaches. In addition, we review studies showing the impact of differing imaging surfaces on T-cell activation.
引用
收藏
页数:7
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