首页> 外文期刊>Journal of biomaterials and nanobiotechnology. >Osteogenesis of MC3T3 Preosteoblasts on 3D Bioactive Peptide Modified Nano-Macroporous Bioactive Glass Scaffolds
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Osteogenesis of MC3T3 Preosteoblasts on 3D Bioactive Peptide Modified Nano-Macroporous Bioactive Glass Scaffolds

机译:3D生物活性肽修饰的纳米巨生物活性玻璃支架上MC3T3成骨细胞的成骨作用。

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Biointerface design that targets osteogenesis is a growing area of research with significant implications in biomedicine. Materials known to either support or stimulate osteogenesis are composed of a biomimetic ceramic material, such as bioactive glass. Bioactive glass is osteoproductive, and the potential for osteoproductivity can be enhanced by the addition of proteins or other additives designed to alter functionality. In addition, soluble growth factors are often added to osteogenic culture on bioactive glasses, further intensifying the effects of the material. In this paper, synthetic peptide combinations, covalently bound to a three-dimensional bioactive glass network, are used to mimic the effects of the whole fibronectin and bone morphogenetic proteins (BMP) 2 and 9. Peptide-silanes possessing critical binding sequences from each of these proteins are synthesized and used to decorate the surface of three-dimensional (3D) nano-macroporous bioactive glass. MC3T3 preosteoblast cells are then assessed for differentiation on the materials in the absence of soluble differentiation cues. MC3T3 preosteoblasts undergo enhanced differentiation on the peptide-silane samples over the standard nano-macroporous bioactive glass, and the differentiation capacity of the cells exposes only to peptide-silane surfaces approaches that of cells grown in chemical differentiation induction media.
机译:针对成骨作用的生物界面设计是一个不断发展的研究领域,对生物医学具有重要意义。已知可支持或刺激成骨作用的材料由仿生陶瓷材料组成,例如生物活性玻璃。生物活性玻璃具有成骨作用,可以通过添加蛋白质或其他旨在改变功能的添加剂来增强成骨作用的潜力。此外,通常将可溶性生长因子添加到生物活性玻璃上的成骨培养物中,从而进一步增强材料的作用。在本文中,共价结合到三维生物活性玻璃网络的合成肽组合用于模拟整个纤连蛋白和骨形态发生蛋白(BMP)2和9的作用。具有各自关键序列的肽硅烷这些蛋白质被合成并用于装饰三维(3D)纳米巨生物活性玻璃的表面。然后在不存在可溶性分化提示的情况下,评估MC3T3前成骨细胞在材料上的分化。 MC3T3前成骨细胞在肽-硅烷样品上比标准的纳米巨生物活性玻璃经历增强的分化,并且细胞的分化能力仅暴露于肽-硅烷表面,接近化学分化诱导培养基中生长的细胞。

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