Panax notoginseng stimulates alkaline phosphatase activity, collagen synthesis, and mineralization in osteoblastic MC3T3-E1 cells

被引:21
作者
Ji, Zhe [1 ]
Cheng, Yizhao [1 ]
Yuan, Puwei [2 ]
Dang, Xiaoqian [1 ]
Guo, Xiong [3 ]
Wang, Weizhuo [1 ]
机构
[1] Xi An Jiao Tong Univ, Affiliated Hosp 2, Dept Orthoped, Xian 710004, Shaanxi, Peoples R China
[2] Shaanxi Tradit Chinese Med Coll, Xianyang 712000, Shaanxi, Peoples R China
[3] Xi An Jiao Tong Univ, Dept Publ Hlth, Hlth Sci Ctr, Key Lab Environm & Genes Related Dis, Xian 710061, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Total saponins of Panax notoginseng; MC3T3-E1; cells; Bone; Osteoporosis; Biomineralization; PERFORMANCE LIQUID-CHROMATOGRAPHY; BONE-FORMATION; IN-VITRO; SAPONINS; DIFFERENTIATION; PROLIFERATION; OSTEOPOROSIS; ANGIOGENESIS; PATHWAYS; RECEPTOR;
D O I
10.1007/s11626-015-9915-x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Total Panax notoginseng saponin (PNS) has been extensively used to treat a variety of diseases, such as bone fractures, soft tissue injuries, etc. In this study, mouse calvaria-original osteoblastic MC3T3-E1 cells were cultured in various concentrations of PNS (0.005-5 mg/mL) during the period (1, 5, 14, and 23 d). At the endpoint, the osteogenic capacity of MC3T3-E1 cells was investigated by measuring the alkaline phosphatase (ALP) activity, the deposited calcium, and the expression of osteogenic-related markers, including bone collagen type 1 (Col1) and osteocalcin (OCN). Compared with all groups in each period, the most pronounced effect was observed at the concentration range between 0.05 and 0.5 mg/mL (P < 0.05) and the cell proliferation with PNS treatment was found during the whole osteogenic period. Moreover, cellular ALP activity with PNS was increased during 7, 14, and 21 d and cell mineralization with PNS was enhanced in 14 and 21 d. Furthermore, the differentiation markers Col1 and OCN increased in the PNS-treated cells. Our work suggests that PNS may stimulate the osteogenesis process which contains osteoblastic proliferation, differentiation, and mineralization by increasing cellular ALP activity, extracellular matrix mineralization, and osteoblast-associated molecules in the osteoblasts.
引用
收藏
页码:950 / 957
页数:8
相关论文
共 40 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]  
Bahlous Afef, 2006, Tunis Med, V84, P751
[4]   Minireview:: Targeting the Wnt/β-catenin pathway to regulate bone formation in the adult skeleton [J].
Baron, Roland ;
Rawadi, Georges .
ENDOCRINOLOGY, 2007, 148 (06) :2635-2643
[5]   Megakaryocytes modulate osteoblast synthesis of type-1 collagen, osteoprotegerin, and RANKL [J].
Bord, S ;
Frith, E ;
Ireland, DC ;
Scott, MA ;
Craig, JIO ;
Compston, JE .
BONE, 2005, 36 (05) :812-819
[6]   ROLE AND REGULATION OF RUNX2 IN OSTEOGENESIS [J].
Bruderer, M. ;
Richards, R. G. ;
Alini, M. ;
Stoddart, M. J. .
EUROPEAN CELLS & MATERIALS, 2014, 28 :269-286
[7]   Red yeast rice stimulates osteoblast proliferation and increases alkaline phosphatase activity in MC3T3-E1 cells [J].
Cho, Young-Eun ;
Alcantara, Ethel ;
Kumaran, Santhy ;
Son, Kun-Ho ;
Sohn, Ho-Yong ;
Lee, Jong-Hwa ;
Choi, Chung-Sig ;
Ha, Tae-Youl ;
Kwun, In-Sook .
NUTRITION RESEARCH, 2010, 30 (07) :501-510
[8]   Increased bone formation in osteocalcin-deficient mice [J].
Ducy, P ;
Desbois, C ;
Boyce, B ;
Pinero, G ;
Story, B ;
Dunstan, C ;
Smith, E ;
Bonadio, J ;
Goldstein, S ;
Gundberg, C ;
Bradley, A ;
Karsenty, G .
NATURE, 1996, 382 (6590) :448-452
[9]  
Duquet N, 2014, J Pharm Belg, P14
[10]   Angiogenesis: from plants to blood vessels [J].
Fan, Tai-Ping ;
Yeh, Ju-Ching ;
Leung, Kar Wah ;
Yue, Patrick Y. K. ;
Wong, Ricky N. S. .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2006, 27 (06) :297-309