RRC ID 63804
著者 Seong CH, Chiba N, Kusuyama J, Subhan Amir M, Eiraku N, Yamashita S, Ohnishi T, Nakamura N, Matsuguchi T.
タイトル Bone morphogenetic protein 9 (BMP9) directly induces Notch effector molecule Hes1 through the SMAD signaling pathway in osteoblasts.
ジャーナル FEBS Lett
Abstract 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.
巻・号 595(3)
ページ 389-403
公開日 2021-2-1
DOI 10.1002/1873-3468.14016
PMID 33264418
MeSH Animals Animals, Newborn Autocrine Communication Base Sequence Cell Differentiation Feedback, Physiological Gene Expression Regulation, Developmental Growth Differentiation Factor 2 / genetics* Growth Differentiation Factor 2 / metabolism Humans Mice Mice, Inbred C57BL Osteoblasts / cytology Osteoblasts / metabolism* Osteocalcin / genetics Osteocalcin / metabolism Osteogenesis / genetics Primary Cell Culture Promoter Regions, Genetic Ribosomal Proteins / genetics Ribosomal Proteins / metabolism Signal Transduction / genetics* Skull / cytology Skull / metabolism Smad6 Protein / genetics Smad6 Protein / metabolism Smad7 Protein / genetics* Smad7 Protein / metabolism Transcription Factor HES-1 / genetics* Transcription Factor HES-1 / metabolism
IF 3.057
リソース情報
ヒト・動物細胞 MC3T3-E1(RCB1126)