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通过T细胞受体 - 共受体拉链进行胸腺选择的亲和力阈值。

Affinity threshold for thymic selection through a T-cell receptor-co-receptor zipper.

作者信息

Palmer Ed, Naeher Dieter

机构信息

Department of Nephrology and Biomedicine, Laboratory of Transplantation Immunology, University Hospital Basel, Basel, Switzerland.

出版信息

Nat Rev Immunol. 2009 Mar;9(3):207-13. doi: 10.1038/nri2469.

Abstract

The affinity of the T-cell receptor (TCR) for self antigen is the basis for the selection of a useful (MHC-restricted) and safe (self-tolerant) T-cell repertoire. However, it has been difficult to understand how thymocytes measure ligand affinity and translate this signal into a cellular response. In this Opinion article, we propose a new model that describes how the TCR discriminates between low- and high-affinity ligands, which is based on the duration of TCR-ligand interactions and a 'zipper' mechanism that mediates the interaction of the TCR and co-receptor molecules to initiate negative-selection signalling.

摘要

T细胞受体(TCR)对自身抗原的亲和力是选择有用的(MHC限制性)和安全的(自身耐受)T细胞库的基础。然而,一直难以理解胸腺细胞如何测量配体亲和力并将该信号转化为细胞反应。在这篇观点文章中,我们提出了一个新模型,该模型描述了TCR如何区分低亲和力和高亲和力配体,其基于TCR-配体相互作用的持续时间以及一种“拉链”机制,该机制介导TCR与共受体分子的相互作用以启动阴性选择信号。

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