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  • 标题:Matrix Protein Biglycan Induces Osteoblast Differentiation through Extracellular Signal-Regulated Kinase and Smad Pathways
  • 本地全文:下载
  • 作者:Xiaoyan Wang ; Kenichi Harimoto ; Sijia Xie
  • 期刊名称:Biological and Pharmaceutical Bulletin
  • 印刷版ISSN:0918-6158
  • 电子版ISSN:1347-5215
  • 出版年度:2010
  • 卷号:33
  • 期号:11
  • 页码:1891-1897
  • DOI:10.1248/bpb.33.1891
  • 出版社:The Pharmaceutical Society of Japan
  • 摘要:Biglycan (Bgn) is a member of the small leucine-rich proteoglycan (SLRP) family found in bone extracellular matrix (ECM), and hence involved in regulating bone formation and matrix mineralization. It has been reported that Bgn facilitates osteoblast differentiation, and extracellular signal-regulated kinase (Erk) and Smad are two important pathways in regulating osteoblast differentiation. However, the underlying mechanism for Bgn facilitating osteoblast differentiation has not been fully elucidated. The present study demonstrated that the matrix protein Bgn activates Erk signaling pathway and therefore increases Runx2 transcriptional activity, in which glycosaminoglycans (GAGs) chains play an essential role. Additionally, Bgn also activated Smad pathway, another signaling pathway related with osteoblast differentiation. The activation of these two signaling pathways induced by Bgn facilitated the mineralization deposition in vitro . These results demonstrated the mechanism of Bgn promoting osteoblast differentiation and matrix mineralization.
  • 关键词:osteoblast;Biglycan;extracellular signal-regulated kinase;Runx2;mineralization
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