Signaling in thymic selection

被引:75
作者
Gascoigne, Nicholas R. J. [1 ]
Palmer, Ed [2 ,3 ]
机构
[1] Scripps Res Inst, Dept Immunol & Microbial Sci, La Jolla, CA 92037 USA
[2] Univ Basel Hosp, Dept Nephrol, Lab Transplantat Immunol, CH-4031 Basel, Switzerland
[3] Univ Basel Hosp, Dept Biomed, CH-4031 Basel, Switzerland
基金
欧洲研究理事会; 瑞士国家科学基金会;
关键词
T-CELL-RECEPTOR; THYMOCYTE POSITIVE SELECTION; NEGATIVE SELECTION; ANTIGEN RECEPTOR; AFFINITY THRESHOLD; SELF-PEPTIDES; ACTIVATION; AGONIST; LIGANDS; BINDING;
D O I
10.1016/j.coi.2010.12.017
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 cell receptor signaling allows the developing thymocyte to undergo positive or negative selection, which is required for the formation of a useful mature T cell repertoire. Recent developments include the finding that much of the Lck kinase (required to initiate T cell signaling) is already in an active configuration before signaling. The analog strength of antigen binding to the T cell receptor binding may be translated into a digital signal by the amount of time the TCR is paired with a co-receptor carrying Lck. Downstream, the cellular localization of MAP kinase signaling is determined by the strength of the signal and in turn predicts positive or negative selection. A novel protein, Themis, is important in crossing the positive selection developmental checkpoint, but its mode of action is still uncertain. Commitment to the CD4 or CD8 lineage is influenced by the amount of ZAP-70 signaling and also by closely regulated responsiveness to intrathymic cytokines such as IL7.
引用
收藏
页码:207 / 212
页数:6
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