骨钙素
肝素
化学
骨形态发生蛋白2
骨形态发生蛋白
细胞生物学
碱性磷酸酶
体外
MAPK/ERK通路
运行x2
骨形态发生蛋白7
成骨细胞
受体
磷酸化
生物化学
生物
酶
基因
作者
Shin Kanzaki,Tetsu Takahashi,Takahiro Kanno,Wataru Ariyoshi,Kouhei Shinmyouzu,Toshiyuki Tujisawa,Tatsuji Nishihara
摘要
Abstract Heparin demonstrates several kinds of biological activities by binding to various extracellular molecules and plays pivotal roles in bone metabolism. However, the role of heparin in the biological activity of bone morphogenetic protein (BMP) remains unclear. In the present study, we examined whether heparin has the effects on osteoblast differentiation induced by BMP‐2 in vitro and also elucidated the precise mechanism by which heparin regulates bone metabolism induced by this molecule. Our results showed that heparin inhibited alkaline phosphatase (ALP) activity and mineralization in osteoblastic cells cultured with BMP‐2. Heparin was found to suppress the mRNA expressions of osterix, Runx2, ALP and osteocalcin, as well as phosphorylation of Smad1/5/8 and p38 MAPK. Further, heparin bound to both BMP‐2 and BMP receptor (BMPR). These results suggest that heparin suppresses BMP‐2‐BMPR binding, and inhibits BMP‐2 osteogenic activity in vitro. J. Cell. Physiol. 216: 844–850, 2008, © 2008 Wiley‐Liss, Inc.
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