胸腺发育过程中 T 细胞的自身反应性决定了阳性选择的时机。

T cell self-reactivity during thymic development dictates the timing of positive selection.

机构信息

Division of Immunology and Pathogenesis, Department of Molecular and Cell Biology, University of California, Berkeley, Berkeley, United States.

Department of Bioengineering, University of California, Berkeley, Berkeley, United States.

出版信息

Elife. 2021 Apr 22;10:e65435. doi: 10.7554/eLife.65435.

Abstract

Functional tuning of T cells based on their degree of self-reactivity is established during positive selection in the thymus, although how positive selection differs for thymocytes with relatively low versus high self-reactivity is unclear. In addition, preselection thymocytes are highly sensitive to low-affinity ligands, but the mechanism underlying their enhanced T cell receptor (TCR) sensitivity is not fully understood. Here we show that murine thymocytes with low self-reactivity experience briefer TCR signals and complete positive selection more slowly than those with high self-reactivity. Additionally, we provide evidence that cells with low self-reactivity retain a preselection gene expression signature as they mature, including genes previously implicated in modulating TCR sensitivity and a novel group of ion channel genes. Our results imply that thymocytes with low self-reactivity downregulate TCR sensitivity more slowly during positive selection, and associate membrane ion channel expression with thymocyte self-reactivity and progress through positive selection.

摘要

基于自身反应程度的 T 细胞功能调节是在胸腺内的阳性选择过程中建立的,尽管对于自身反应性相对较低和较高的胸腺细胞,阳性选择有何不同尚不清楚。此外,预选胸腺细胞对低亲和力配体非常敏感,但增强 T 细胞受体 (TCR) 敏感性的机制尚不完全清楚。在这里,我们表明,与自身反应性高的细胞相比,低自身反应性的小鼠胸腺细胞经历的 TCR 信号更短,并且完全的阳性选择更慢。此外,我们提供的证据表明,随着成熟,低自身反应性的细胞保留预选的基因表达特征,包括先前被认为调节 TCR 敏感性的基因和一组新的离子通道基因。我们的研究结果表明,在阳性选择过程中,低自身反应性的胸腺细胞下调 TCR 敏感性的速度较慢,并且将膜离子通道表达与胸腺细胞自身反应性和通过阳性选择相关联。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c388/8116051/8c0303fab600/elife-65435-fig1.jpg

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