Abraham S M, Clark A R
Kennedy Institute of Rheumatology Division, Imperial College London, 1 Aspenlea Road, Hammersmith, London W6 8LH, UK.
Biochem Soc Trans. 2006 Dec;34(Pt 6):1018-23. doi: 10.1042/BST0341018.
Innate immune responses are critically dependent on MAPK (mitogen-activated protein kinase) signalling pathways, in particular JNK (c-Jun N-terminal kinase) and p38 MAPK. Both of these kinases are negatively regulated via their dephosphorylation by DUSP1 (dual--specificity phosphatase 1). Several pro- and anti-inflammatory stimuli converge to regulate the DUSP1 gene and to modulate the time course of its expression. In turn, the pattern of expression of DUSP1 dictates the kinetics of activation of JNK and p38 MAPK, and this influences the expression of several mediators of innate immunity. DUSP1 is therefore a central regulator of innate immunity, and its expression can profoundly affect the outcome of inflammatory challenges. We discuss possible implications for immune-mediated inflammatory diseases and their treatment.
先天性免疫反应严重依赖于丝裂原活化蛋白激酶(MAPK)信号通路,特别是c-Jun氨基末端激酶(JNK)和p38 MAPK。这两种激酶都通过双特异性磷酸酶1(DUSP1)的去磷酸化而受到负调控。几种促炎和抗炎刺激共同作用,调节DUSP1基因并调节其表达的时间进程。反过来,DUSP1的表达模式决定了JNK和p38 MAPK的激活动力学,这影响了几种先天性免疫介质的表达。因此,DUSP1是先天性免疫的核心调节因子,其表达可深刻影响炎症刺激的结果。我们讨论了对免疫介导的炎症性疾病及其治疗的可能影响。