自身免疫
基因剔除小鼠
细胞生物学
T细胞
T细胞受体
蛋白质酪氨酸磷酸酶
实验性自身免疫性脑脊髓炎
生物
免疫系统
信号转导
免疫学
癌症研究
受体
遗传学
作者
Ju Pi Li,Chia Yu Yang,Huai Chia Chuang,Joung Liang Lan,Der Yuan Chen,Yi Ming Chen,Xiaohong Wang,Alice J. Chen,John W. Belmont,Tse‐Hua Tan
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.
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