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MKP-1 Is Necessary for T Cell Activation and Function

机译:MKP-1是T细胞激活和功能所必需的

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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.
机译:MAPK是进化上保守的免疫调节剂。负调节MAPK活性的MAPK磷酸酶(MKPs)最近已成为先天和适应性免疫应答中的关键角色。 MKP-1,也称为DUSP1,先前已显示可通过抑制促炎性细胞因子的产生来负调节先天免疫力。在这里,我们发现MKP-1在T细胞激活和功能中是必需的。 T细胞中的MKP-1缺乏会在体外损害T细胞的活化,增殖和功能,这与JNK的活化增强和NFATc1易位进入细胞核减少有关。一致地,MKP-1 -/-小鼠体内抗流感免疫缺陷,对实验性自身免疫性脑脊髓炎有抵抗力。因此,我们的结果证明,MKP-1是T细胞活化和功能的关键正调节剂,可靶向治疗自身免疫性疾病。

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