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首页> 外文期刊>Journal of biomedical materials research. Part B, Applied biomaterials. >The effect of peptide surface density on mineralization of a matrix deposited by osteogenic cells
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The effect of peptide surface density on mineralization of a matrix deposited by osteogenic cells

机译:肽表面密度对成骨细胞沉积的基质矿化的影响

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The density of Arg-Gly-Asp-containing peptides covalently grafted to solid materials has been shown to affect adhesion, spreading, and focal contact formation. The objective of this study was to examine the effect of ligand density on mineralization of the extracellular matrix deposited by osteoblasts. In particular, RGD-modified quartz surfaces with ligand densities varying over two orders (0.01-3.6 pmol/cm~2) of magnitude were prepared to assess the long-term function of osteoblasts on peptide-derivatized surfaces. After 3 weeks in culture, surfaces modified with a 15 amino add peptide (Ac-Cys-Gly-Gly-Asn-Gly-Clu-Pro-Arg-Gly-Asg-Thr-Tyr-Arg-Ala-Tyr-NH_2) at a density >=0.62 pmol/ cm~2 significantly (p < 0.05) enhanced mineralization corn-pared with a RGD surface density of 0.01 pmol/cm~2, RCF surfaces, or clean surfaces adsorbed with serum proteins. These results suggest that regulation of the surface density of adhesive ligands on biomaterial surfaces is a critical determinant in a strategy to alter the degree of extracellular matrix maturation in contact with solid surfaces (e.g., implants). Further studies are required to elucidate the intracellular signal transudation pathways that mediate long-term matrix mineralization through the initial engagement of these adhesive ligands.
机译:已显示共价接枝到固体材料上的含Arg-Gly-Asp肽的密度会影响粘附,扩散和焦点接触的形成。这项研究的目的是检查配体密度对成骨细胞沉积的细胞外基质矿化的影响。特别是,制备了配体密度在两个数量级(0.01-3.6 pmol / cm〜2)之间变化的RGD改性石英表面,以评估成骨细胞在肽衍生化表面上的长期功能。培养3周后,用15个氨基添加肽(Ac-Cys-Gly-Gly-Asn-Gly-Clu-Pro-Arg-Gly-Asg-Thr-Tyr-Arg-Ala-Tyr-NH_2)修饰的表面与RGD表面密度为0.01 pmol / cm〜2,RCF表面或吸附有血清蛋白的清洁表面相比,密度> = 0.62 pmol / cm〜2显着(p <0.05)增强了玉米矿化作用。这些结果表明,调节生物材料表面上的粘合剂配体的表面密度是改变与固体表面(例如植入物)接触的细胞外基质成熟程度的策略中的关键决定因素。需要进一步的研究以阐明通过这些粘合剂配体的初始结合来介导长期基质矿化的细胞内信号渗出途径。

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