Smad8/9 Is Regulated Through the BMP Pathway

被引:21
|
作者
Katakawa, Yuko [1 ]
Funaba, Masayuki [2 ]
Murakami, Masaru [1 ]
机构
[1] Azabu Univ, Sch Vet Med, Mol Biol Lab, Sagamihara, Kanagawa 2525201, Japan
[2] Kyoto Univ, Grad Sch Agr, Div Appl Biosci, Kyoto 6068502, Japan
关键词
BMP; SMAD8; 9; TRANSCRIPTION; TGF-BETA; SIGNALING PATHWAY; I RECEPTOR; CELLS; EXPRESSION; PHOSPHATASE; DOWNSTREAM; INHIBITION; ANTAGONIST; INDUCTION;
D O I
10.1002/jcb.25478
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
Members of the transforming growth factor- (TGF-) family function through Smad-dependent and Smad-independent pathways. The Smad-dependent pathway is stimulated through the phosphorylation of receptor-regulated Smad (R-Smad) and inhibited through the dephosphorylation of R-Smad or the gene induction of inhibitory Smad (I-Smad). Little information is available on the regulation of R-Smad gene expression. BMP4 potentiated the up-regulation of Smad8/9 expression in C2C12, H9c2, 3T3-L1, HepG2, B16, and primary fibroblasts. BMP4-induced Smad8/9 expression was cycloheximide-insensitive and LDN-193189-sensitive, suggesting a direct event mediated through BMP type I receptors. BMP4 transcriptionally stimulated the Smad8/9 gene, and BMP-responsive elements (BREs) spanning nt -121 to nt -44 are involved in the up-regulation of Smad8/9 expression in response to BMP4. Phosphorylated Smad1/5/8/9 specifically bound to the BREs of Smad8/9 gene. The present study reveals that Smad8/9 is a unique R-Smad regulated through the BMP pathway at the mRNA level. J. Cell. Biochem. 117: 1788-1796, 2016. (c) 2016 Wiley Periodicals, Inc.
引用
收藏
页码:1788 / 1796
页数:9
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