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Originally published as MBC in Press, 10.1091/mbc.E05-02-0105 on May 18, 2005

Vol. 16, Issue 7, 3365-3376, July 2005

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Induction of Human NF-IL6{beta} by Epidermal Growth Factor Is Mediated through the p38 Signaling Pathway and cAMP Response Element-binding Protein Activation in A431 Cells

Ju-Ming Wang, Joseph T. Tseng, and Wen-Chang Chang

Department of Pharmacology, College of Medicine, National Cheng Kung University, Tainan 701, Taiwan

Submitted February 22, 2005; Revised May 3, 2005; Accepted May 5, 2005
Monitoring Editor: Carl-Henrik Heldin

The CCAAT/enhancer binding protein {delta} (C/EBP{delta}, CRP3, CELF, NF-IL6{beta}) regulates gene expression and plays functional roles in many tissues, such as in acute phase response to inflammatory stimuli, adipocyte differentiation, and mammary epithelial cell growth control. In this study, we examined the expression of human C/EBP{delta} (NF-IL6{beta}) gene by epidermal growth factor (EGF) stimulation in human epidermoid carcinoma A431 cells. NF-IL6{beta} was an immediate-early gene activated by the EGF-induced signaling pathways in cells. By using 5'-serial deletion reporter analysis, we showed that the region comprising the –347 to +9 base pairs was required for EGF response of the NF-IL6{beta} promoter. This region contains putative consensus binding sequences of Sp1 and cAMP response element-binding protein (CREB). The NF-IL6{beta} promoter activity induced by EGF was abolished by mutating the sequence of cAMP response element or Sp1 sites in the –347/+9 base pairs region. Both in vitro and in vivo DNA binding assay revealed that the CREB binding activity was low in EGF-starved cells, whereas it was induced within 30 min after EGF treatment of A431 cells. However, no change in Sp1 binding activity was found by EGF treatment. Moreover, the phosphatidylinositol 3 (PI3)-kinase inhibitor (wortmannin) and p38MAPK inhibitor (SB203580) inhibited the EGF-induced CREB phosphorylation and the expression of NF-IL6{beta} gene in cells. We also demonstrated that CREB was involved in regulating the NF-IL6{beta} gene transcriptional activity mediated by p38MAPK. Our results suggested that PI3-kinase/p38MAPK/CREB pathway contributed to the EGF activation of NF-IL6{beta} gene expression.


This article was published online ahead of print in MBC in Press (http://www.molbiolcell.org/cgi/doi/10.1091/mbc.E05–02–0105) on May 18, 2005.

Abbreviations used: ChIP, chromatin immunoprecipitation; CRE, cAMP response element; CREB, cAMP response element-binding protein; EGF, epidermal growth factor; MAPK, mitogen-activated protein kinase.

Address correspondence to: Wen-Chang Chang (wcchang{at}mail.ncku.edu.tw).




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