Rosa Adalberto L, Beloti Márcio M
Department of Oral and Maxillofacial Surgery and Periodontology, School of Dentistry of Ribeirao Preto, University of Sao Paulo, Av. do Cafe, s/n, 14040-904- Ribeirao Preto, SP, Brazil.
Biomaterials. 2003 Aug;24(17):2927-32. doi: 10.1016/s0142-9612(03)00129-7.
TAK-778 induces bone growth in in vitro and in vivo models. The aim of this study was to evaluate the osteogenic potential of TAK-778 on human bone marrow cells cultured on commercially pure titanium (cpTi). Cells were cultured either in absence or in presence of TAK-778 (10(-5)M) on cpTi in supplemented alpha-MEM. For attachment evaluation, cells were cultured for 4 and 24h. After 7, 14, and 21 days, cell proliferation, cell viability, total protein content, alkaline phosphatase (ALP) activity, and bone-like formation were evaluated. TAK-778 did not affect cell attachment and viability. Cell number was reduced by TAK-778. ALP activity, total protein content, and bone-like formation were increased by TAK-778. These results suggest that initial cell events such as cell attachment are not affected by TAK-778 while events that indicate osteoblast differentiation including reduced cell proliferation, and increased both ALP activity and bone-like formation are enhanced by TAK-778 in presence of cpTi. It means that TAK-778 could be a useful drug to improve the osseointegration of implants by both enhancing and accelerating bone formation on Ti surface.
TAK-778在体外和体内模型中均可诱导骨生长。本研究旨在评估TAK-778对在商业纯钛(cpTi)上培养的人骨髓细胞的成骨潜力。细胞在添加了α-MEM的cpTi上,分别在不存在或存在TAK-778(10⁻⁵M)的情况下进行培养。为了评估细胞黏附情况,细胞培养4小时和24小时。在培养7天、14天和21天后,评估细胞增殖、细胞活力、总蛋白含量、碱性磷酸酶(ALP)活性和类骨形成情况。TAK-778不影响细胞黏附和活力。TAK-778使细胞数量减少。TAK-778使ALP活性、总蛋白含量和类骨形成增加。这些结果表明,诸如细胞黏附等初始细胞事件不受TAK-778影响,而在cpTi存在的情况下,TAK-778可增强包括细胞增殖减少以及ALP活性和类骨形成增加等表明成骨细胞分化的事件。这意味着TAK-778可能是一种通过增强和加速钛表面的骨形成来改善植入物骨整合的有用药物。