IL-1β-stimulated activation of ERK1/2 and p38α MAPK mediates the transcriptional up-regulation of IL-6, IL-8 and GRO-α in HeLa cells

被引:48
|
作者
Yang, Huei-Ting [1 ]
Cohen, Philip [1 ]
Rousseau, Simon [1 ]
机构
[1] Univ Dundee, Coll Life Sci, Sir James Black Ctr, MRC Prot Phosphorylat Unit, Dundee DD1 5EH, Scotland
基金
英国医学研究理事会;
关键词
IL-1; receptor; chemokine; MAP kinase; inflammation; epithelial cells;
D O I
10.1016/j.cellsig.2007.10.025
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Epithelial cells represent the first line of defense against infection. Here we have studied the production of inflammatory mediators induced by IL-1 beta in the HeLa epithelial cell line. We found that GRO-alpha, IL-6 and IL-8 were the only three inflammatory mediators elevated out of 36 tested. Specific inhibition of p38 alpha MAP kinase or preventing the activation of ERK1/ERK2 partially reduced the production of these substances, while the combined blockade of both pathways almost abolished secretion. The suppression of these signaling pathways mainly reduced transcription of the genes encoding GRO-alpha, IL-6 and IL-8, rather than affecting mRNA stability, translation or secretion. The production of these three inflammatory mediators was shown to account for the ability of the HeLa cell culture medium to stimulate the migration of monocytes/macrophages, suggesting a key role for p38 MATK and ERK1/ERK2 in orchestrating die epithelial cell response to infection. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:375 / 380
页数:6
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