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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.
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页码:7135 / 7139
页数:5
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