Division of Experimental Immunology, Institute of Advanced Medical Sciences, University of Tokushima, Tokushima, Japan.
Thymus Biology Section, Experimental Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD, United States.
Adv Immunol. 2021;149:1-23. doi: 10.1016/bs.ai.2021.03.001. Epub 2021 May 1.
Functionally competent and self-tolerant T cell repertoire is shaped through positive and negative selection in the cortical and medullary microenvironments of the thymus. The thymoproteasome specifically expressed in the cortical thymic epithelium is essential for the optimal generation of CD8 T cells. Although how the thymoproteasome governs the generation of CD8 T cells is not fully understood, accumulating evidence suggests that the thymoproteasome optimizes CD8 T cell production through the processing of self-peptides associated with MHC class I molecules expressed by cortical thymic epithelial cells. In this review, we describe recent advances in the mechanism of thymoproteasome-dependent generation of CD8 T cells, focusing on the process of cortical positive selection independent of apoptosis-mediated negative selection.
功能性成熟且自身耐受的 T 细胞库是通过胸腺皮质和髓质微环境中的阳性选择和阴性选择而形成的。在皮质胸腺上皮细胞中特异性表达的胸腺蛋白酶体对于 CD8 T 细胞的最佳产生是必需的。尽管胸腺蛋白酶体如何调控 CD8 T 细胞的产生尚不完全清楚,但越来越多的证据表明,胸腺蛋白酶体通过加工与皮质胸腺上皮细胞表达的 MHC Ⅰ类分子相关的自身肽来优化 CD8 T 细胞的产生。在这篇综述中,我们描述了胸腺蛋白酶体依赖性 CD8 T 细胞产生机制的最新进展,重点介绍了不依赖凋亡介导的阴性选择的皮质阳性选择过程。