Regulation of CD8+ T cell development by thymus-specific proteasomes

被引:452
作者
Murata, Shigeo [1 ]
Sasaki, Katsuhiro
Kishimoto, Toshihiko
Niwa, Shin-ichiro
Hayashi, Hidemi
Takahama, Yousuke
Tanaka, Keiji
机构
[1] Tokyo Metropolitan Inst Med Sci, Lab Frontier Sci Core Technol & Res Ctr, Bunkyo Ku, Tokyo 1138613, Japan
[2] Japan Sci & TEchnol Agcy, Precursory Res Embryon Sci & Technol, Kawaguchi, Saitama 3320012, Japan
[3] Toho Univ, Fac Sci, Proteome Anal Ctr, Chiba 2748510, Japan
[4] Toho Univ, Fac Sci, Dept Biomol Sci, Chiba 2748510, Japan
[5] Link Genom, Chuo Ku, Tokyo 1030024, Japan
[6] Univ Tokushima, Grad Sch Med Sci, Inst Genome Res, Div Expt Immunol, Tokushima 7708503, Japan
关键词
D O I
10.1126/science.1141915
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 beta 5t. beta 5t 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 beta 5t into proteasomes in place of beta 5 or beta 5i selectively reduces this activity. We also found that beta 5t-deficient mice displayed defective development of CD8(+) T cells in the thymus. Our results suggest a key role for beta 5t in generating the MHC class I-restricted CD8(+) T cell repertoire during thymic selection.
引用
收藏
页码:1349 / 1353
页数:5
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