Department of Immunology and Microbial Science, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
Curr Opin Immunol. 2011 Apr;23(2):207-12. doi: 10.1016/j.coi.2010.12.017. Epub 2011 Jan 15.
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.
T 细胞受体信号允许发育中的胸腺细胞经历阳性或阴性选择,这是形成有用的成熟 T 细胞库所必需的。最近的研究进展包括发现,在信号转导之前,大部分 Lck 激酶(启动 T 细胞信号转导所需)已经处于活跃构象。T 细胞受体结合的抗原结合的模拟强度可以通过 TCR 与携带 Lck 的共受体配对的时间长短转化为数字信号。在下游,MAP 激酶信号的细胞定位由信号的强度决定,并反过来预测阳性或阴性选择。一种新的蛋白质,Themis,在跨越阳性选择发育检查点方面很重要,但它的作用模式仍不确定。CD4 或 CD8 谱系的决定受到 ZAP-70 信号的数量以及对胸腺内细胞因子(如 IL7)的反应性的紧密调节的影响。