Thymoproteasomes produce unique peptide motifs for positive selection of CD8+ T cells

被引:75
|
作者
Sasaki, Katsuhiro [1 ]
Takada, Kensuke [2 ]
Ohte, Yuki [1 ]
Kondo, Hiroyuki [2 ]
Sorimachi, Hiroyuki [3 ]
Tanaka, Keiji [4 ]
Takahama, Yousuke [2 ]
Murata, Shigeo [1 ]
机构
[1] Univ Tokyo, Lab Prot Metab, Grad Sch Pharmaceut Sci, Tokyo 1130033, Japan
[2] Univ Tokushima, Inst Genome Res, Div Expt Immunol, Tokushima 7708503, Japan
[3] Tokyo Metropolitan Inst Med Sci, Dept Adv Sci Biomol, Calpain Project, Tokyo 1568506, Japan
[4] Tokyo Metropolitan Inst Med Sci, Lab Prot Metab, Tokyo 1568506, Japan
来源
NATURE COMMUNICATIONS | 2015年 / 6卷
关键词
CLASS-I MOLECULES; 2.4 ANGSTROM RESOLUTION; 20S PROTEASOME; SUBSTRATE-SPECIFICITY; NEGATIVE SELECTION; THYMIC SELECTION; MHC; COMPLEX; ANTIGEN; IDENTIFICATION;
D O I
10.1038/ncomms8484
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
Positive selection in the thymus provides low-affinity T-cell receptor (TCR) engagement to support the development of potentially useful self-major histocompatibility complex class I (MHC-I)-restricted T cells. Optimal positive selection of CD8(+) T cells requires cortical thymic epithelial cells that express beta 5t-containing thymoproteasomes (tCPs). However, how tCPs govern positive selection is unclear. Here we show that the tCPs produce unique cleavage motifs in digested peptides and in MHC-I-associated peptides. Interestingly, MHC-I-associated peptides carrying these tCP-dependent motifs are enriched with low-affinity TCR ligands that efficiently induce the positive selection of functionally competent CD8(+) T cells in antigen-specific TCR-transgenic models. These results suggest that tCPs contribute to the positive selection of CD8(+) T cells by preferentially producing low-affinity TCR ligand peptides.
引用
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页数:10
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