细胞生物学
激酶
MAPK/ERK通路
蛋白激酶A
转录因子
免疫系统
NFAT公司
生物
p38丝裂原活化蛋白激酶
效应器
免疫学
信号转导
化学
磷酸酶
磷酸化
生物化学
基因
作者
Kate L. Jeffrey,Tilman Brummer,Michael S. Rolph,Sue Min Liu,Nuria A. Callejas,Raelene J. Grumont,Corine Gilliéron,Fabienne Mackay,Shane T. Grey,Montserrat Camps,Christian Rommel,Steve Gerondakis,Charles R. Mackay
摘要
Mitogen-activated protein kinases facilitate many cellular processes and are essential for immune cell function. Their activity is controlled by kinases and dual-specificity phosphatases. A comprehensive microarray analysis of human leukocytes identified DUSP2 (encoding the phosphatase PAC-1) as one of the most highly induced transcripts in activated immune cells. We generated Dusp2(-/-) mice and found considerably reduced inflammatory responses in the 'K/BxN' model of rheumatoid arthritis. PAC-1 deficiency led to increased activity of Jun kinase (Jnk) but unexpected impairment of the activity of extracellular signal-regulated kinase (Erk) and the kinase p38, reduced activity of the transcription factor Elk1 and a complex of mobilized transcription factor NFAT and the AP-1 transcription factor and decreased effector immune cell function. Thus, PAC-1 is a key positive regulator of inflammatory cell signaling and effector functions, mediated through Jnk and Erk mitogen-activated protein kinase crosstalk.
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