Transcriptional regulation of mouse mast cell protease-7 by TGF-β

被引:13
|
作者
Funaba, M
Ikeda, T
Murakami, M
Ogawa, K
Nishino, Y
Tsuchida, K
Sugino, H
Abe, M
机构
[1] Azabu Univ, Sch Vet Med, Lab Nutr, Sagamihara, Kanagawa 2298501, Japan
[2] Azabu Univ, Sch Vet Med, Lab Pathobiochem & Immunol, Sagamihara, Kanagawa 2298501, Japan
[3] Azabu Univ, Sch Vet Med, Mol Biol Lab, Sagamihara, Kanagawa 2298501, Japan
[4] RIKEN, Lab Cellular Biochem, Wako, Saitama 3510198, Japan
[5] Univ Tokushima, Inst Enzyme Res, Tokushima 7708503, Japan
基金
日本学术振兴会;
关键词
Smad3; Smad4; c-fos; c-jun;
D O I
10.1016/j.bbaexp.2006.04.003
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
Mouse mast cell protease-7 (mincp-7) is a tryptase predominantly expressed in differentiated connective tissue-type mast cells. Previous study revealed that transforming growth factor-beta (TGF-beta) increases gene transcript of mmcp-7 in mast cells. The present study explored molecular mechanism of the up-regulation of mmcp-7 by TGF-beta. Luciferase-based reporter assays using deletion and point mutations of mmcp-7 promoter showed a critical region spanning nt - 126 to - 122 relative to the transcriptional start site, a Smad-binding element, for transcriptional activation by the TGF-beta pathway. In addition, a region from nt - 104 to -98, a TPA-responsive element, was also necessary for the transactivation. Consistent with the current model for the TGF-beta signaling, Smad4 was required for the transcription of mmcp-7 by Smad3, a signal mediator of TGF-beta. Treatment with TGF-beta in mast cells resulted in the differential gene induction of the AP-1 components, i.e., transient induction of c-fos but not of c-jun and junB. Expression of c-fos further enhanced Smad3 and Smad4-induced transcription of mmcp-7, whereas c-jun expression inhibited the transcription. Our results suggest that TGF-beta stimulates mmcp-7 transcription through the Smad3-Smad4 pathway as well as c-fos induction, and that the AP-1 components distinctly related with the TGF-beta pathway. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:166 / 170
页数:5
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