Calycosin-7-O-β-D-glucopyranoside stimulates osteoblast differentiation through regulating the BMP/WNT signaling pathways

被引:39
作者
Jian, Jing [1 ]
Sun, Lijuan [1 ]
Cheng, Xun [1 ]
Hu, Xiaofang [1 ]
Liang, Jichao [1 ]
Chen, Yong [1 ]
机构
[1] Hubei Univ, Hubei Prov Key Lab Biotechnol Chinese Tradit Med, Hubei Collaborat Innovat Ctr Green Transformat Bi, Wuhan 430062, Peoples R China
基金
中国国家自然科学基金;
关键词
BMP singnaling pathway; WNT/beta-catenin signaling pathway; Osteoblastic differentiation; Calycosin-7-O-beta-D-glucopyranoside; ST2; cells; OVARIECTOMIZED RATS; BONE-DISEASES; IN-VITRO; EXPRESSION; ASTRAGALUS; CATENIN; OSTEOPOROSIS; LINEAGE; CELLS; BMP-2;
D O I
10.1016/j.apsb.2015.06.005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The isoflavone calycosin-7-O-beta-D-glucopyranoside (CG) is a principal constituent Astragalus membranceus (AR) and has been reported to inhibit osteoclast development in vitro and bone loss in vivo. The aim of this study was to investigate the osteogenic effects of CG and its underlying mechanism in ST2 cells. The resulsts show that exposure of cells to CG in osteogenic mineralization process. Mechanistically, CG treatment increased the expression of bone morphogenetic progtein 2 (BMP-2), p-Smad 1/5/8, beta-catenin and Runx2, all of which are regulateors of the BMP- or wingless-type MMTV pathways, respecively. Taken together, the results indicate that CG promotes the osteoblastic differentiation of ST2 cells through regulating the BN1P/WNT signaling pathways. On this basis, CG may he a useful lead compound for improving the treatment of hone decreasing diseases and enhancing bone regeneration. (c) 2015 Chinese Pharmaceutical Association and Institute of Materia Medic, Chinese Academy of Sciences. Production and hosting by Elsevier B.V.
引用
收藏
页码:454 / 460
页数:7
相关论文
共 34 条
[1]  
Aubin JE, 1998, J CELL BIOCHEM, P73, DOI 10.1002/(SICI)1097-4644(1998)72:30/31+<73::AID-JCB11>3.0.CO
[2]  
2-L
[3]   Salidroside stimulates osteoblast differentiation through BMP signaling pathway [J].
Chen, Jin-Jing ;
Zhang, Nian-Fei ;
Mao, Gen-Xiang ;
He, Xiao-Bo ;
Zhan, Yue-Chen ;
Deng, Hong-Bin ;
Song, Dan-Qing ;
Li, Dian-Dong ;
Li, Zhuo-Rong ;
Si, Shu-Yi ;
Qiu, Qiang ;
Wang, Zhen .
FOOD AND CHEMICAL TOXICOLOGY, 2013, 62 :499-505
[4]  
Choi S, 2005, J MICROBIOL BIOTECHN, V15, P1258
[5]   Wnt/β-catenin signaling in mesenchymal progenitors controls osteoblast and chondrocyte differentiation during vertebrate skeletogenesis [J].
Day, TF ;
Guo, XZ ;
Garrett-Beal, L ;
Yang, YZ .
DEVELOPMENTAL CELL, 2005, 8 (05) :739-750
[6]   Osf2/Cbfa1: A transcriptional activator of osteoblast differentiation [J].
Ducy, P ;
Zhang, R ;
Geoffroy, V ;
Ridall, AL ;
Karsenty, G .
CELL, 1997, 89 (05) :747-754
[7]   Structural basis of BMP signalling inhibition by the cystine knot protein Noggin [J].
Groppe, J ;
Greenwald, J ;
Wiater, E ;
Rodriguez-Leon, J ;
Economides, AN ;
Kwiatkowski, W ;
Affolter, M ;
Vale, WW ;
Belmonte, JCI ;
Choe, S .
NATURE, 2002, 420 (6916) :636-642
[8]  
최수임, 2003, Korean Society for Biotechnology and Bioengineering Journal, V18, P282
[9]   Essential role of β-catenin in postnatal bone acquisition [J].
Holmen, SL ;
Zylstra, CR ;
Mukherjee, A ;
Sigler, RE ;
Faugere, MC ;
Bouxsein, ML ;
Deng, LF ;
Clemens, TL ;
Williams, BO .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (22) :21162-21168
[10]   Icaritin and its glycosides enhance osteoblastic, but suppress osteoclastic, differentiation and activity in vitro [J].
Huang, Jian ;
Yuan, Lan ;
Wang, Xi ;
Zhang, Tian-Lan ;
Wang, Kui .
LIFE SCIENCES, 2007, 81 (10) :832-840