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

被引:76
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
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.
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页数:10
相关论文
共 49 条
[1]   Involvement of Bag6 and the TRC pathway in proteasome assembly [J].
Akahane, Takashi ;
Sahara, Kazutaka ;
Yashiroda, Hideki ;
Tanaka, Keiji ;
Murata, Shigeo .
NATURE COMMUNICATIONS, 2013, 4
[2]   INTERFERON-GAMMA INDUCES DIFFERENT SUBUNIT ORGANIZATIONS AND FUNCTIONAL DIVERSITY OF PROTEASOMES [J].
AKI, M ;
SHIMBARA, N ;
TAKASHINA, M ;
AKIYAMA, K ;
KAGAWA, S ;
TAMURA, T ;
TANAHASHI, N ;
YOSHIMURA, T ;
TANAKA, K ;
ICHIHARA, A .
JOURNAL OF BIOCHEMISTRY, 1994, 115 (02) :257-269
[3]   Identification of the yeast 20S proteasome catalytic centers and subunit interactions required for active-site formation [J].
Arendt, CS ;
Hochstrasser, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (14) :7156-7161
[4]   CD5 expression is developmentally regulated by T cell receptor (TCR) signals and TCR avidity [J].
Azzam, HS ;
Grinberg, A ;
Lui, K ;
Shen, H ;
Shores, EW ;
Love, PE .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (12) :2301-2311
[5]   26S proteasomes and immunoproteasomes produce mainly N-extended versions of an antigenic peptide [J].
Cascio, P ;
Hilton, C ;
Kisselev, AF ;
Rock, KL ;
Goldberg, AL .
EMBO JOURNAL, 2001, 20 (10) :2357-2366
[6]   Thymic selection threshold defined by compartmentalization of Ras/MAPK signalling [J].
Daniels, Mark A. ;
Teixeiro, Emma ;
Gill, Jason ;
Hausmann, Barbara ;
Roubaty, Dominique ;
Holmberg, Kaisa ;
Werlen, Guy ;
Hollaender, Georg A. ;
Gascoigne, Nicholas R. J. ;
Palmer, Ed .
NATURE, 2006, 444 (7120) :724-729
[7]  
DICK LR, 1994, J IMMUNOL, V152, P3884
[8]   MHC-LINKED LMP GENE-PRODUCTS SPECIFICALLY ALTER PEPTIDASE ACTIVITIES OF THE PROTEASOME [J].
DRISCOLL, J ;
BROWN, MG ;
FINLEY, D ;
MONACO, JJ .
NATURE, 1993, 365 (6443) :262-264
[9]   STRUCTURE OF PEPTIDES ASSOCIATED WITH MHC CLASS-I MOLECULES [J].
ENGELHARD, VH .
CURRENT OPINION IN IMMUNOLOGY, 1994, 6 (01) :13-23
[10]   Recognition and Processing of Ubiquitin-Protein Conjugates by the Proteasome [J].
Finley, Daniel .
ANNUAL REVIEW OF BIOCHEMISTRY, 2009, 78 :477-513