细胞生物学
生物
先天免疫系统
MAPK/ERK通路
免疫系统
获得性免疫系统
T细胞
实验性自身免疫性脑脊髓炎
免疫
免疫学
功能(生物学)
信号转导
作者
Yongliang Zhang,Joseph M. Reynolds,Seon Hee Chang,Natalia Martín‐Orozco,Yeonseok Chung,Roza Nurieva,Chen Dong
标识
DOI:10.1074/jbc.m109.052472
摘要
MAPKs are evolutionarily conserved immune regulators. MAPK phosphatases (MKPs) that negatively regulate MAPK activities have recently emerged as critical players in both innate and adaptive immune responses. MKP-1, also known as DUSP1, was previously shown to negatively regulate innate immunity by inhibiting pro-inflammatory cytokine production. Here, we found that MKP-1 is necessary in T cell activation and function. MKP-1 deficiency in T cells impaired the activation, proliferation, and function of T cells in vitro, associated with enhanced activation of JNK and reduced NFATc1 translocation into the nucleus. Consistently, MKP-1(-/-) mice were defective in anti-influenza immunity in vivo and resistant to experimental autoimmune encephalomyelitis. Our results thus demonstrate that MKP-1 is a critical positive regulator of T cell activation and function and may be targeted in treatment of autoimmune diseases.
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