The effect of purmorphamine on osteoblast phenotype expression of human bone marrow mesenchymal cells cultured on titanium

被引:17
作者
Beloti, MM [1 ]
Bellesini, LS [1 ]
Rosa, AL [1 ]
机构
[1] Univ Sao Paulo, Dept Oral & Maxillofacial Surg & Periodontol, Sch Dent Ribeirao Preto, BR-14040904 Ribeirao Preto, SP, Brazil
关键词
cell differentiation; human bone marrow mesenchymal cells; osteoblast; purmorphamine; titanium;
D O I
10.1016/j.biomaterials.2004.10.039
中图分类号
R318 [生物医学工程];
学科分类号
0831 [生物医学工程];
摘要
Purmorphamine is a new molecule with osteogenesis-inducing activity in multipotent progenitor cells. The aim of this study was to evaluate whether purmorphamine maintains its osteogenic potential on human bone marrow mesenchymal cells cultured on commercially pure titanium (cpTi). Cells were cultured either in the absence or presence of purmorphamine 3 mum on cpTi in supplemented alpha-MEM. At 7, 14, and 21 days, cell proliferation, viability, total protein content, collagen content, and alkaline phosphatase (ALP) activity were evaluated. Bone-like nodule formation was evaluated at 21 days. All experiments were done in quintuplicate and data were compared by ANOVA or t-test. Purmorphamine did not affect cell proliferation (P = 0.619), viability (p = 0.831), and collagen content (p = 0.088). Total protein content (p = 0.047), ALP activity (l) = 0.001), and bone-like nodule formation (p = 0.002) were increased by purmorphamine. The present results indicate that events related to osteoblast, differentiation, including increased ALP activity and bone-like nodule formation, are enhanced by purmorphamine in the presence of cpTi. It means that this molecule could be useful as an adjunct therapy to improve the osseointegration of the implants in the fields of dentistry and orthopaedics. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4245 / 4248
页数:4
相关论文
共 10 条
[1]
Beloti MM, 2004, FUND CLIN PHARMACOL, V18, P104
[2]
BOLANDER ME, 1992, P SOC EXP BIOL MED, V200, P165
[3]
[4]
A combinatorial scaffold approach toward kinase-directed heterocycle libraries [J].
Ding, S ;
Gray, NS ;
Wu, X ;
Ding, Q ;
Schultz, PG .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (08) :1594-1596
[5]
LOWRY OH, 1951, J BIOL CHEM, V193, P265
[6]
Synthesis of novel 2-benzothiopyran and 3-benzothiepin derivatives and their stimulatory effect on bone formation [J].
Oda, T ;
Notoya, K ;
Gotoh, M ;
Taketomi, S ;
Fujisawa, Y ;
Makino, H ;
Sohda, T .
JOURNAL OF MEDICINAL CHEMISTRY, 1999, 42 (04) :751-760
[7]
A simplified method for the analysis of hydroxyproline in biological tissues [J].
Reddy, GK ;
Enwemeka, CS .
CLINICAL BIOCHEMISTRY, 1996, 29 (03) :225-229
[8]
Rosa Adalberto Luiz, 2003, Braz. Dent. J., V14, P16, DOI 10.1590/S0103-64402003000100003
[9]
UNDERLYING MECHANISMS AT THE BONE-BIOMATERIAL INTERFACE [J].
SCHWARTZ, Z ;
BOYAN, BD .
JOURNAL OF CELLULAR BIOCHEMISTRY, 1994, 56 (03) :340-347
[10]
A small molecule with osteogenesis-inducing activity in multipotent mesenchymal progenitor cells [J].
Wu, X ;
Ding, S ;
Ding, Q ;
Gray, NS ;
Schultz, PG .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (49) :14520-14521