Cutting edge:: Regulation of T cell activation threshold by CD28 costimulation through targeting Cbl-b for ubiquitination

被引:111
作者
Zhang, J
Bárdos, T
Li, DD
Gál, I
Vermes, C
Xu, JY
Mikecz, K
Finnegan, A
Lipkowitz, S
Glant, TT
机构
[1] Rush Med Coll, Sect Mol Med, Dept Orthoped Surg, Rush Presbyterian St Lukes Med Ctr, Chicago, IL 60612 USA
[2] Rush Med Coll, Rush Presbyterian St Lukes Med Ctr, Dept Internal Med, Chicago, IL 60612 USA
[3] Rush Med Coll, Rush Presbyterian St Lukes Med Ctr, Dept Biochem, Chicago, IL 60612 USA
[4] Rush Med Coll, Rush Presbyterian St Lukes Med Ctr, Dept Immunol Microbiol, Chicago, IL 60612 USA
[5] NCI, Med Branch, Dept Genet, Bethesda, MD 20889 USA
关键词
D O I
10.4049/jimmunol.169.5.2236
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Optimal T cell activation requires signaling through the TCR and CD28 costimulatory receptor. CD28 costimulation is believed to set the threshold for T cell activation. Recently, Cbl-b, a ubiquitin ligase, has been shown to negatively regulate CD28-dependent T cell activation. In this report, we show that CD28 costimulation selectively induces greater ubiquitination and degradation of Cbl-b in wild-type T cells than CD3 stimulation alone, and TCR-induced Cbl-b ubiquitination and degradation are significantly reduced in CD28-deficient T cells. Stimulation of CD28-deficient T cells with higher doses of anti-CD3 results in increased ubiquitination of Cbl-b, which correlates with enhanced T cell responses. Our results demonstrate that CD28 costimulation regulates the threshold for T cell activation, at least in part, by promoting Cbl-b ubiquitination and degradation.
引用
收藏
页码:2236 / 2240
页数:5
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