The Phosphatase PTP-PEST Promotes Secondary T Cell Responses by Dephosphorylating the Protein Tyrosine Kinase Pyk2

被引:54
|
作者
Davidson, Dominique [1 ]
Shi, Xiaochu [1 ]
Zhong, Ming-Chao [1 ]
Rhee, Inmoo [1 ,2 ]
Veillette, Andre [1 ,2 ,3 ]
机构
[1] Clin Res Inst Montreal, Mol Oncol Lab, Montreal, PQ H2W 1R7, Canada
[2] McGill Univ, Dept Med, Montreal, PQ H3G 1Y6, Canada
[3] Univ Montreal, Dept Med, Montreal, PQ H3C 3J7, Canada
基金
加拿大健康研究院;
关键词
ANTIGEN RECEPTOR; ADHESION; ACTIVATION; INHIBITION; TOLERANCE; BETA; MICE; GENE; PEP; STIMULATION;
D O I
10.1016/j.immuni.2010.08.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
PTP-PEST (encoded by Ptpn12) is an intracellular protein tyrosine phosphatase belonging to the same family as LYP. LYP inhibits secondary T cell responses by suppressing Src family protein tyrosine kinases and is implicated in human autoimmunity. To determine the function of PTP-PEST in T cells, we generated mice with a conditionally deleted allele of Ptpn12. By removing PIP-PEST in T cells, we determined that PTP-PEST was not necessary for T cell development or primary responses. However, PTP-PEST was required for secondary T cell responses, anergy prevention, and autoimmunity induction. PTP-PEST specifically regulated the phosphorylation of Pyk2, a substrate of the Src family kinase Fyn. It also promoted the formation of T cell homoaggregates, which are known to enhance T cell activation. Thus, PTP-PEST controls Pyk2 activity and is a positive regulator of secondary T cell activation. These data illustrate the critical role of protein tyrosine phosphatases in T cell regulation.
引用
收藏
页码:167 / 180
页数:14
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