Zhang Jian, Bárdos Tamás, Li Dongdong, Gál István, Vermes Csaba, Xu Jianye, Mikecz Katalin, Finnegan Alison, Lipkowitz Stan, Glant Tibor T
Section of Molecular Medicine, Department of Orthopedic Surgery, Rush Medical College at Rush-Presbyterian-St. Luke's Medical Center, Chicago, IL 60612, USA.
J Immunol. 2002 Sep 1;169(5):2236-40. doi: 10.4049/jimmunol.169.5.2236.
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.
最佳的T细胞活化需要通过TCR和CD28共刺激受体进行信号传导。CD28共刺激被认为设定了T细胞活化的阈值。最近,泛素连接酶Cbl-b已被证明对CD28依赖性T细胞活化具有负调节作用。在本报告中,我们表明,与单独的CD3刺激相比,CD28共刺激在野生型T细胞中选择性地诱导更高水平的Cbl-b泛素化和降解,并且在CD28缺陷型T细胞中,TCR诱导的Cbl-b泛素化和降解显著减少。用更高剂量的抗CD3刺激CD28缺陷型T细胞会导致Cbl-b泛素化增加,这与增强的T细胞反应相关。我们的结果表明,CD28共刺激至少部分地通过促进Cbl-b泛素化和降解来调节T细胞活化的阈值。