The phosphatase JKAP/DUSP22 inhibits T-cell receptor signalling and autoimmunity by inactivating Lck

被引:118
|
作者
Li, Ju-Pi [1 ]
Yang, Chia-Yu [1 ]
Chuang, Huai-Chia [1 ]
Lan, Joung-Liang [2 ,3 ,4 ]
Chen, Der-Yuan [2 ,5 ]
Chen, Yi-Ming [2 ,5 ]
Wang, Xiaohong [6 ]
Chen, Alice J. [6 ]
Belmont, John W. [7 ]
Tan, Tse-Hua [1 ,6 ]
机构
[1] Natl Hlth Res Inst, Immunol Res Ctr, Zhunan 35053, Taiwan
[2] Taichung Vet Gen Hosp, Div Rheumatol Allergy & Immunol, Taichung 40705, Taiwan
[3] China Med Univ, Dept Med, Taichung 40402, Taiwan
[4] China Med Univ Hosp, Dept Internal Med, Div Rheumatol & Immunol, Taichung 40402, Taiwan
[5] Natl Yang Ming Univ, Fac Med, Taipei 11221, Taiwan
[6] Baylor Coll Med, Dept Pathol & Immunol, Houston, TX 77030 USA
[7] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
来源
NATURE COMMUNICATIONS | 2014年 / 5卷
关键词
PROTEIN-TYROSINE PHOSPHATASES; DUAL-SPECIFICITY PHOSPHATASE; THYMOCYTE DEVELOPMENT; THERAPEUTIC TARGETS; ACTIVATION; CD45; PHOSPHORYLATION; PROLIFERATION; MECHANISMS; SITES;
D O I
10.1038/ncomms4618
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
JNK pathway-associated phosphatase (JKAP, also known as DUSP22 or JSP-1) is a JNK activator. The in vivo role of JKAP in immune regulation remains unclear. Here we report that JKAP directly inactivates Lck by dephosphorylating tyrosine-394 residue during T-cell receptor (TCR) signalling. JKAP-knockout T cells display enhanced cell proliferation and cytokine production. JKAP-knockout mice show enhanced T-cell-mediated immune responses and are more susceptible to experimental autoimmune encephalomyelitis (EAE). In addition, the recipient mice that are adoptively transferred with JKAP-knockout T cells show exacerbated EAE symptoms. Aged JKAP-knockout mice spontaneously develop inflammation and autoimmunity. Thus, our results indicate that JKAP is an important phosphatase that inactivates Lck in the TCR signalling turn-off stage, leading to suppression of T-cell-mediated immunity and autoimmunity.
引用
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页数:13
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