Insights into the initiation of TCR signaling

被引:282
作者
Chakraborty, Arup K. [1 ,2 ,3 ,4 ,5 ,6 ]
Weiss, Arthur [7 ,8 ]
机构
[1] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
[2] MIT, Dept Phys, Cambridge, MA 02139 USA
[3] MIT, Dept Chem, Cambridge, MA 02139 USA
[4] MIT, Dept Biol Engn, Cambridge, MA 02139 USA
[5] MIT, Inst Med Engn & Sci, Cambridge, MA 02139 USA
[6] Ragon Inst MGH MIT & Harvard, Cambridge, MA USA
[7] Univ Calif San Francisco, Rosalind Russell Ephraim P Engleman Rheumatol Res, Div Rheumatol, Dept of Med, San Francisco, CA 94143 USA
[8] Univ Calif San Francisco, Howard Hughes Med Inst, San Francisco, CA USA
基金
美国国家卫生研究院;
关键词
T-CELL-RECEPTOR; TYROSINE-PROTEIN-KINASE; PROLINE-RICH SEQUENCE; ANTIGEN RECEPTOR; NEGATIVE REGULATION; PHOSPHATASE CD45; STRUCTURAL BASIS; B-CELL; ACTIVATION; PEPTIDE;
D O I
10.1038/ni.2940
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
The initiation of T cell antigen receptor signaling is a key step that can result in T cell activation and the orchestration of an adaptive immune response. Early events in T cell receptor signaling can distinguish between agonist and endogenous ligands with exquisite selectivity, and show extraordinary sensitivity to minute numbers of agonists in a sea of endogenous ligands. We review our current knowledge of models and crucial molecules that aim to provide a mechanistic explanation for these observations. Building on current understanding and a discussion of unresolved issues, we propose a molecular model for initiation of T cell receptor signaling that may serve as a useful guide for future studies.
引用
收藏
页码:798 / 807
页数:10
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