Bone morphogenetic protein 9 (BMP9) directly induces Notch effector molecule Hes1 through the SMAD signaling pathway in osteoblasts

被引:7
|
作者
Seong, Chang-Hwan [1 ,2 ]
Chiba, Norika [2 ]
Kusuyama, Joji [2 ,3 ,4 ]
Amir, Muhammad Subhan [1 ,2 ,5 ]
Eiraku, Nahoko [6 ]
Yamashita, Sachiko [2 ]
Ohnishi, Tomokazu [2 ]
Nakamura, Norifumi [1 ]
Matsuguchi, Tetsuya [2 ]
机构
[1] Kagoshima Univ, Grad Sch Med & Dent Sci, Dept Oral & Maxillofacial Surg, Kagoshima, Japan
[2] Kagoshima Univ, Grad Sch Med & Dent Sci, Dept Oral Biochem, Kagoshima, Japan
[3] Harvard Med Sch, Joslin Diabet Ctr, Dept Med, Sect Integrat Physiol & Metab, Boston, MA 02115 USA
[4] Tohoku Univ, Frontier Res Inst Interdisciplinary Sci, Sendai, Miyagi, Japan
[5] Airlangga Univ, Fac Dent, Dept Oral & Maxillofacial Surg, Surabaya, Indonesia
[6] Kagoshima Univ, Grad Sch Med & Dent Sci, Dept Periodontol, Kagoshima, Japan
关键词
Bone Morphogenetic Protein 9; bone regeneration; Hes1; notch; osteogenic differentiation; BMP9-INDUCED OSTEOGENIC DIFFERENTIATION; TGF-BETA; NEGATIVE AUTOREGULATION; RESPONSIVE ELEMENT; GENE-EXPRESSION; IDENTIFICATION; TRANSCRIPTION; CELLS; ACTIVATION; INHIBITION;
D O I
10.1002/1873-3468.14016
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
Bone morphogenetic protein (BMP) 9 is one of the most osteogenic BMPs, but its mechanism of action has not been fully elucidated. Hes1, a transcriptional regulator with a basic helix-loop-helix domain, is a well-known effector of Notch signaling. Here, we find that BMP9 induces periodic increases of Hes1 mRNA and protein expression in osteoblasts, presumably through an autocrine negative feedback mechanism. BMP9-mediated Hes1 induction is significantly inhibited by an ALK inhibitor and overexpression of Smad7, an inhibitory Smad. Luciferase and ChIP assays revealed that two Smad-binding sites in the 5 ' upstream region of the mouse Hes1 gene are essential for transcriptional activation by BMP9. Thus, our data indicate that BMP9 induces Hes1 expression in osteoblasts via the Smad signaling pathway.
引用
收藏
页码:389 / 403
页数:15
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