Departamento de Biologia, Facultad de Ciencias, Universidad de Chile, Santiago, Chile Fundacion Ciencia para la Vida, Santiago, Chile.
Scand J Immunol. 2012 Apr;75(4):389-400. doi: 10.1111/j.1365-3083.2012.02673.x.
The Notch signalling pathway regulates several aspects of cellular differentiation such as T lineage commitment and effector functions on peripheral T cells; however, there is limited information regarding Notch receptor expression on different T cell subsets and the putative role of the different receptors on T cell effector function. Here, we studied the protein expression of Notch receptors on murine T cells in vitro and in vivo and analysed the role of the Notch pathway in cytokine production by CD4+ and CD8+ T cells. We found that resting CD4+ and CD8+ T cells do not express Notch receptors, but they upregulate Notch 1 and Notch 2 shortly after in vitro and in vivo activation. Using a γ-secretase inhibitor, which blocks Notch signalling through all Notch receptors, we demonstrated that the Notch pathway regulates IL-10 production by CD4+ T cells and IFN-γ and IL-17 production by CD8+ T cells. These results suggest that Notch 1 and 2 are expressed by CD4+ and CD8+ T cells and represent the putative Notch receptors that regulate effector functions and cytokine production by these cells.
Notch 信号通路调节细胞分化的几个方面,如 T 细胞谱系的决定和外周 T 细胞的效应功能;然而,关于 Notch 受体在不同 T 细胞亚群上的表达以及不同受体在 T 细胞效应功能上的潜在作用的信息有限。在这里,我们研究了 Notch 受体在体外和体内的小鼠 T 细胞上的蛋白表达,并分析了 Notch 通路在 CD4+和 CD8+T 细胞细胞因子产生中的作用。我们发现静止的 CD4+和 CD8+T 细胞不表达 Notch 受体,但它们在体外和体内激活后不久就上调 Notch1 和 Notch2。使用一种 γ-分泌酶抑制剂,它通过所有 Notch 受体阻断 Notch 信号,我们证明 Notch 通路调节 CD4+T 细胞的 IL-10 产生以及 CD8+T 细胞的 IFN-γ 和 IL-17 产生。这些结果表明,Notch1 和 Notch2 由 CD4+和 CD8+T 细胞表达,代表调节这些细胞效应功能和细胞因子产生的潜在 Notch 受体。