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首页> 外文期刊>Clinical oral implants research >Effect of recombinant human bone morphogenetic protein-7 (rhBMP-7) on the viability, proliferation and differentiation of osteoblast-like cells cultured on a chemically modified titanium surface.
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Effect of recombinant human bone morphogenetic protein-7 (rhBMP-7) on the viability, proliferation and differentiation of osteoblast-like cells cultured on a chemically modified titanium surface.

机译:重组人骨形态发生蛋白7(rhBMP-7)对化学修饰的钛表面上培养的成骨细胞样细胞的活力,增殖和分化的影响。

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AIM: The aim of the present study was to assess the influence of the chemical characteristics and roughness of titanium surfaces on the viability, proliferation and differentiation of osteoblast-like cells cultured in a medium supplemented with recombinant human bone morphogenetic protein-7 (rhBMP-7). MATERIAL AND METHODS: Osteo-1 cells were grown on titanium disks presenting with the following surfaces: (1) machined, (2) coarse grit-blasted and acid-attacked (SLA) and (3) chemically modified SLA (SLAmod) in the absence or presence of 20 ng/ml rhBMP-7 in culture medium. The viability and number of osteo-1 cells were evaluated after 24 h. Analyses of total protein content (TP) and alkaline phosphatase (AP) activity at 7, 14 and 21 days, collagen content at 7 and 21 days and mineralized matrix formation at 21 days were performed. RESULTS: Cell viability (P=0.5516), cell number (P=0.3485), collagen content (P=0.1165) and mineralized matrix formation (P=0.5319) were not affected by the different surface configurations or by the addition of rhBMP-7 to the medium. Osteo-1 cells cultured on SLA surfaces showed a significant increase in TP at 21 days. The ALPase/TP ratio (P=0.00001) was affected by treatment and time. CONCLUSION: The results suggest that the addition of rhBMP-7 to the culture medium did not exert any effect on the viability, proliferation or differentiation of osteoblast-like cells grown on the different surfaces tested. All titanium surfaces analyzed allowed the complete expression of the osteoblast phenotype such as matrix mineralization by osteo-1 cells.
机译:目的:本研究旨在评估钛表面化学特性和粗糙度对在重组人骨形态发生蛋白7(rhBMP-)培养基中培养的成骨样细胞的活力,增殖和分化的影响。 7)。材料与方法:Osteo-1细胞在具有以下表面的钛圆片上生长:(1)机械加工,(2)粗粒喷砂和酸攻击(SLA)和(3)经过化学修饰的SLA(SLAmod)。培养基中是否存在20 ng / ml rhBMP-7。 24小时后评估osteo-1细胞的活力和数量。在第7、14和21天分析总蛋白含量(TP)和碱性磷酸酶(AP)活性,在7和21天分析胶原蛋白含量,在21天分析矿化基质的形成。结果:细胞活力(P = 0.5516),细胞数(P = 0.3485),胶原蛋白含量(P = 0.1165)和矿化基质形成(P = 0.5319)不受不同的表面构型或添加rhBMP-7的影响到中等。在SLA表面培养的Osteo-1细胞在21天时TP显着增加。 ALPase / TP比(P = 0.00001)受治疗和时间影响。结论:结果表明,向培养基中添加rhBMP-7不会对在不同测试表面上生长的成骨样细胞的活力,增殖或分化产生任何影响。分析的所有钛表面允许成骨细胞表型的完整表达,例如由osteo-1细胞矿化的基质。

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