P38 MAPK signaling pathway is involved in butyrate-induced vitamin D receptor expression

被引:26
作者
Daniel, C [1 ]
Schröder, O [1 ]
Zahn, N [1 ]
Gaschott, T [1 ]
Stein, J [1 ]
机构
[1] Univ Frankfurt, Dept Med 2, ZAFES, D-6000 Frankfurt, Germany
关键词
butyrate; Caco-2; cells; cell differentiation; p38 MAP kinase; ERK1/2 MAP kinase; vitamin D receptor; PD98059; SB203580;
D O I
10.1016/j.bbrc.2004.09.191
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Previously, we have demonstrated that the butyrate-induced differentiation in the human colon cancer cell line Caco-2 occurs via upregulation of the vitamin D receptor (VDR). However, the downstream pathways involved are unknown. The mitogen-activated protein kinases (MAPKs) have been shown to play an important role in regulation of cell differentiation, and may therefore be a potential target of butyrate action. To assess their role in butyrate-mediated cell differentiation and VDR expression, we used the specific p38-MAPK inhibitor SB203580 and the ERK1/2 MAPK-inhibitor PD98059. The p38-MAPK inhibitor abolished the butyrate effect on VDR expression and cell differentiation, while the ERK1/2 inhibitor did not influence the butyrate-mediated induction of cell differentiation and VDR expression. The essential role of the p38 pathway in up-regulation of VDR expression was further confirmed by using the p38 stimulator arsenite. These results imply an important role of the p38-MAPK in regulation of cellular differentiation through upregulation of VDR expression by butyrate. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:1220 / 1226
页数:7
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