Murata Shigeo, Sasaki Katsuhiro, Kishimoto Toshihiko, Niwa Shin-Ichiro, Hayashi Hidemi, Takahama Yousuke, Tanaka Keiji
Laboratory of Frontier Science, Core Technology and Research Center, Tokyo Metropolitan Institute of Medical Science, Bunkyo-ku, Tokyo 113-8613, Japan.
Science. 2007 Jun 1;316(5829):1349-53. doi: 10.1126/science.1141915.
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 beta5t. beta5t 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 beta5t into proteasomes in place of beta5 or beta5i selectively reduces this activity. We also found that beta5t-deficient mice displayed defective development of CD8(+) T cells in the thymus. Our results suggest a key role for beta5t in generating the MHC class I-restricted CD8(+) T cell repertoire during thymic selection.
蛋白酶体负责生成由免疫系统的I类主要组织相容性复合体(MHC)分子呈递的肽段。在此,我们报告鉴定出一种先前未被识别的催化亚基,称为β5t。β5t仅在皮质胸腺上皮细胞中表达,这些细胞负责发育中胸腺细胞的阳性选择。尽管蛋白酶体的类胰凝乳蛋白酶活性被认为对于产生与MHC I类裂隙具有高亲和力的肽段很重要,但用β5t取代β5或β5i掺入蛋白酶体中会选择性地降低这种活性。我们还发现,β5t缺陷小鼠在胸腺中表现出CD8(+) T细胞发育缺陷。我们的结果表明,β5t在胸腺选择过程中生成MHC I类限制性CD8(+) T细胞库中起关键作用。