Moriggl R, Sexl V, Piekorz R, Topham D, Ihle J N
Howard Hughes Medical Institute, St. Jude Children's Research Hospital, Memphis, Tennessee 38105, USA.
Immunity. 1999 Aug;11(2):225-30. doi: 10.1016/s1074-7613(00)80097-7.
The activation and subsequent proliferation of peripheral T cells requires the engagement of the T cell and a cytokine receptor, typically the IL-2 or IL-4 receptors. Critical to understanding the regulation of peripheral T cells is the knowledge of the unique contributions of each receptor to full T cell activation and cell cycle progression. Mice deficient in Stat5a and Stat5b have demonstrated the essential role that these highly related proteins play in cell cycle progression following peripheral T cell activation. Here we demonstrate that activation of the Stat5 proteins by tyrosine phosphorylation is uniquely contributed by cytokine receptor signaling and specifically does not occur through the T cell receptor complex.
外周T细胞的激活及随后的增殖需要T细胞与细胞因子受体结合,通常是IL-2或IL-4受体。了解外周T细胞的调节机制的关键在于了解每个受体对T细胞完全激活和细胞周期进程的独特作用。Stat5a和Stat5b基因敲除小鼠已证明这些高度相关的蛋白质在T细胞外周激活后的细胞周期进程中所起的重要作用。在此我们证明,Stat5蛋白的酪氨酸磷酸化激活是由细胞因子受体信号通路独特贡献的,而不是通过T细胞受体复合物发生的。