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Regulation of CD8~+ T Cell Development by Thymus-Specific Proteasomes

机译:胸腺特异性蛋白酶体对CD8〜+ T细胞发育的调节

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Proteasomes are responsible for generating peptides presented by the class Ⅰ major histocompatibility complex (MHC) molecules of the immune system. Here, we report the identification of a previously unrecognized catalytic subunit called β5t. β5t is expressed exclusively in cortical thymic epithelial cells, which are responsible for the positive selection of developing thymocytes. Although the chymotrypsin-like activity of proteasomes is considered to be important for the production of peptides with high affinities for MHC class Ⅰ clefts, incorporation of β5t into proteasomes in place of β5 or β5i selectively reduces this activity. We also found that p5t-deficient mice displayed defective development of CD8~+ T cells in the thymus. Our results suggest a key role for β5t in generating the MHC class Ⅰ-restricted CD8~+ T cell repertoire during thymic selection.
机译:蛋白酶体负责产生由免疫系统的Ⅰ类主要组织相容性复合体(MHC)分子呈递的肽。在这里,我们报告了一个先前未被识别的催化亚基称为β5t的鉴定。 β5t仅在皮质胸腺上皮细胞中表达,负责上皮胸腺细胞的阳性选择。尽管认为蛋白酶体的胰凝乳蛋白酶样活性对于产生对MHCⅠ类裂口具有高亲和力的肽很重要,但将β5t掺入蛋白酶体代替β5或β5i选择性地降低了该活性。我们还发现,p5t缺陷小鼠在胸腺中显示CD8〜+ T细胞发育不良。我们的结果表明,β5t在胸腺选择过程中在产生MHCⅠ类限制性CD8〜+ T细胞库中起着关键作用。

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