Cutting edge:: Cbl-b:: One of the key molecules tuning CD28- and CTLA-4-Mediated T cell costimulation

被引:89
作者
Li, DD
Gál, I
Vermes, C
Alegre, ML
Chong, ASF
Chen, LP
Shao, Q
Adarichev, V
Xu, XM
Koreny, T
Mikecz, K
Finnegan, A
Glant, TT
Zhang, J
机构
[1] Univ Chicago, Dept Med, Nephrol Sect, Chicago, IL 60637 USA
[2] Univ Chicago, Dept Surg, Chicago, IL 60637 USA
[3] Rush Univ, Med Ctr, Dept Orthoped Surg, Chicago, IL 60612 USA
[4] Rush Univ, Med Ctr, Dept Biochem, Chicago, IL 60612 USA
[5] Rush Univ, Med Ctr, Dept Internal Med, Chicago, IL 60612 USA
[6] Rush Univ, Med Ctr, Dept Microbiol Immunol, Chicago, IL 60612 USA
[7] Mayo Clin & Mayo Fdn, Dept Immunol, Rochester, MN 55905 USA
[8] Univ Western Ontario, Dept Anat & Cell Biol, London, ON, Canada
关键词
D O I
10.4049/jimmunol.173.12.7135
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Cbl-b negatively regulates CD28-dependent T cell activation. In this report, we tested the hypothesis that CD28 and CTLA-4 have opposite roles in tuning T cell activation threshold by controlling the levels of Cbl-b protein expression. We demonstrate that CD28 costimulation potentiates TCR-induced Chl-b degradation, whereas CTLA-4-B7 interaction is required for Cbl-b re-expression. In support of this finding, Cbl-b expression in CTLA-4 knockout (KO) T cells is significantly reduced, and treating CTLA-4KO mice with human CTLA-4Ig to block CD28-B7 interaction restores Cbl-b expression on T cells. Furthermore, CD28 and CTLA-4 costimulatory effects are compromised in Cbl-bKO T cells. These observations indicate that CD28 and CTLA-4 tightly regulate Cbl-b expression which is critical for establishing the threshold for T cell activation.
引用
收藏
页码:7135 / 7139
页数:5
相关论文
共 33 条
[1]   CD28-mediated co-stimulation: A quantitative support for TCR signalling [J].
Acuto, O ;
Michel, F .
NATURE REVIEWS IMMUNOLOGY, 2003, 3 (12) :939-951
[2]   T-cell regulation by CD28 and CTLA-4 [J].
Alegre, ML ;
Frauwirth, KA ;
Thompson, CB .
NATURE REVIEWS IMMUNOLOGY, 2001, 1 (03) :220-228
[3]   Negative regulation of lymphocyte activation and autoimmunity by the molecular adaptor Cbl-b [J].
Bachmaier, K ;
Krawczyk, C ;
Kozieradzki, I ;
Kong, YY ;
Sasaki, T ;
Oliveira-dos-Santos, A ;
Mariathasan, S ;
Bouchard, D ;
Wakeham, A ;
Itie, A ;
Le, J ;
Ohashi, PS ;
Sarosi, I ;
Nishina, H ;
Lipkowitz, S ;
Penninger, JM .
NATURE, 2000, 403 (6766) :211-216
[4]   Distinct roles for LFA-1 and CD28 during activation of naive T cells: Adhesion versus costimulation [J].
Bachmann, MF ;
McKallFaienza, K ;
Schmits, R ;
Bouchard, D ;
Beach, J ;
Speiser, DE ;
Mak, TW ;
Ohashi, PS .
IMMUNITY, 1997, 7 (04) :549-557
[5]   The B7 family of ligands and its receptors: New pathways for costimulation and inhibition of immune responses [J].
Carreno, BM ;
Collins, M .
ANNUAL REVIEW OF IMMUNOLOGY, 2002, 20 :29-53
[6]   CTLA-4-mediated inhibition in regulation of T cell responses: Mechanisms and manipulation in tumor immunotherapy [J].
Chambers, CA ;
Kuhns, MS ;
Egen, JG ;
Allison, JP .
ANNUAL REVIEW OF IMMUNOLOGY, 2001, 19 :565-594
[7]   The expanding world of co-stimulation: the two-signal model revisited [J].
Chambers, CA .
TRENDS IN IMMUNOLOGY, 2001, 22 (04) :217-223
[8]   Cbl-b regulates the CD28 dependence of T-cell activation [J].
Chiang, YPJ ;
Kole, HK ;
Brown, K ;
Naramura, M ;
Fukuhara, S ;
Hu, RJ ;
Jang, IK ;
Gutkind, JS ;
Shevach, E ;
Gu, H .
NATURE, 2000, 403 (6766) :216-220
[9]   Negative regulation of T cell receptor-lipid raft interaction by cytotoxic T lymphocyte-associated antigen 4 [J].
Chikuma, S ;
Imboden, JB ;
Bluestone, JA .
JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 197 (01) :129-135
[10]   The expanding B7 superfamily: Increasing complexity in costimulatory signals regulating T cell function [J].
Coyle, AJ ;
Gutierrez-Ramos, JC .
NATURE IMMUNOLOGY, 2001, 2 (03) :203-209