Regulation of Drosophila p38 activation by specific MAP2 kinase and MAP3 kinase in response to different stimuli

被引:38
作者
Zhuang, ZH
Zhou, Y
Yu, MC
Silverman, N
Ge, BX
机构
[1] Chinese Acad Sci, Shanghai Inst Biol Sci, Shanghai 200025, Peoples R China
[2] Shanghai Med Univ 2, Joint Immunol Lab, Hlth Sci Ctr, Shanghai 200025, Peoples R China
[3] Shanghai Med Univ 2, Shanghai Inst Immunol, Shanghai 200025, Peoples R China
[4] Shanghai Univ E Inst, Shanghai 200025, Peoples R China
[5] Univ Massachusetts, Sch Med, Dept Med, Div Infect Dis, Worcester, MA 01605 USA
关键词
Drosophila; p38; MEKK1; TAK1; PGN; RNAi;
D O I
10.1016/j.cellsig.2005.05.013
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The p38 mitogen-activated protein kinase (MAPK) signaling pathway plays an important role in cellular responses to inflammatory stimuli and environmental stress. Activation of p38 is mediated through phosphorylation by upstream MAPKK, which in turn is activated by MAPKKK. However, the mechanism of how different upstream MAP2Ks and MAP3Ks specifically contribute to p38 activation in response to different stimuli is still not clearly understood. By using double-stranded RNA-mediated interference (RNAi) in Drosophila cells, we demonstrate that D-NKK3 is a major MAP2K responsible for D-p38 activation by UV, heat shock, NaCl or peptiodglycan (PGN). Stimulation of UV and PGN activates D-p38 through D-MEKK1, heat shock-induced activation of D-p38 signals through both D-MEKK1 and D-ASK1. On the other hand, maximal activation of D-p38 by NaCl requires the expression of four MAP3Ks.
引用
收藏
页码:441 / 448
页数:8
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