Stat5 activation is uniquely associated with cytokine signaling in peripheral T cells

被引:133
|
作者
Moriggl, R
Sexl, V
Piekorz, R
Topham, D
Ihle, JN [1 ]
机构
[1] St Jude Childrens Res Hosp, Howard Hughes Med Inst, Memphis, TN 38105 USA
[2] St Jude Childrens Res Hosp, Dept Biochem, Memphis, TN 38105 USA
[3] St Jude Childrens Res Hosp, Dept Immunol, Memphis, TN 38105 USA
[4] Univ Tennessee, Sch Med, Dept Biochem, Memphis, TN 38063 USA
关键词
D O I
10.1016/S1074-7613(00)80097-7
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页码:225 / 230
页数:6
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