Department of Internal Medicine, Washington University School of Medicine, St Louis, MO 63110.
J Immunol. 2014 Apr 15;192(8):3465-9. doi: 10.4049/jimmunol.1301240. Epub 2014 Mar 17.
CD28 is a critical regulator of T cell function, augmenting proliferation, cytokine secretion, and cell survival. Our previous work using knockin mice expressing point mutations in CD28 demonstrated that the distal proline motif was primarily responsible for much of CD28 function, whereas in marked contrast to prior studies, mutation of the PI3K-binding motif had little discernible effect. In this study, we examined the phenotype of mice in which both motifs are simultaneously mutated. We found that mutation of the PYAP motif unmasks a critical role for the proximal tyrosine motif in regulating T cell proliferation and expression of Bcl-xL but not cytokine secretion. In addition, we demonstrated that, although function is more severely impaired in the double mutant than in either single mutant, there remained residual CD28-dependent responses, definitively establishing that additional motifs can partially mediate CD28 function.
CD28 是 T 细胞功能的关键调节因子,可增强增殖、细胞因子分泌和细胞存活。我们之前使用表达 CD28 点突变的基因敲入小鼠的研究表明,远端脯氨酸基序主要负责 CD28 的大部分功能,而与先前的研究形成鲜明对比的是,PI3K 结合基序的突变几乎没有明显影响。在这项研究中,我们检查了两个基序同时突变的小鼠表型。我们发现,PYAP 基序的突变揭示了近端酪氨酸基序在调节 T 细胞增殖和 Bcl-xL 表达中的关键作用,但对细胞因子分泌没有影响。此外,我们证明,尽管双突变体的功能比单个突变体严重受损,但仍存在残留的 CD28 依赖性反应,明确证实了其他基序可以部分介导 CD28 功能。