Apoptosis signal-regulating kinase 1 in leukotriene D4-induced activator protein-1 activation in airway smooth muscle cells

被引:10
|
作者
Kumasawa, F
Hashimoto, S
Onose, A
Jibiki, I
Mizumura, K
Matsumoto, K
Maruoka, S
Gon, Y
Kobayashi, T
Takahashi, N
Ichijo, H
Horie, T
机构
[1] Nihon Univ, Sch Med, Dept Internal Med, Div Resp Med,Itabashi Ku, Tokyo 1737610, Japan
[2] Univ Tokyo, Grad Sch Pharmaceut Sci, Lab Cell Signaling, Tokyo, Japan
关键词
LTD4; ASK1; AP-1; airway smooth muscle cells; remodeling;
D O I
10.1016/j.ejphar.2005.05.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cysteinyl leukotrienes (LTs) are involved in allergic disorders including bronchial asthma. Transcription factor activator protein-1 (AP-1) activation is essential for cell proliferation and differentiation. LTD4 is shown to promote human airway smooth muscle cell proliferation; however, the effect of LTD4 on AP-1 activation in airway smooth muscle cells and the molecular mechanism in regulating AP-1 activation have not been determined. We examined the effect LTD4 on AP-1 activation in human airway smooth muscle cells and analyzed a role of apoptosis signal-regulating kinase1 (ASK1), an upstream kinase kinase of c-Jun-NH2-terminal kinase (JNK) and p38 mitogen-activated protein kinase (MAPK) in LTD4-induced AP-1 activation to clarify the signaling molecule regulating AP-1 activation. The results showed that LTD4 induced AP-1 activation determined by AP-1-dependent luciferase gene activity and ASK1 phosphorylation. Transient transfection of the dominant negative form of ASK1 attenuated LTD4-induced AP-1 activation. In addition, LTD4-induced AP-1 activity was depressed in the dominant negative form of ASK1-stably transfected porcine artery endothelial cells compared to that in the parental porcine artery endothelial cells. These results indicate that LTD4 is capable of inducing AP-1 activation and ASK1 regulates AP-1 activation in LTD4-stimulated airway smooth muscle cells. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:11 / 16
页数:6
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