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首页> 外文期刊>Key Engineering Materials >Preliminary Results of in vitro Study of Cell Growth in a 45S5 Bioactive Glass as Bone Substitute using Scanning Electron and Confocal Microscopies
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Preliminary Results of in vitro Study of Cell Growth in a 45S5 Bioactive Glass as Bone Substitute using Scanning Electron and Confocal Microscopies

机译:使用扫描电子和共聚焦显微镜在45S5生物活性玻璃作为骨替代品中细胞生长的体外研究的初步结果

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摘要

The aim of this study was to evaluate the cytocompatibility, cell ingrowth and extracellular matrix deposition of a newly developed porous bioactive glass as a bone substitute. Two types of bioactive glass, different in their pore size (75 and 20 ppi, resp. ~350 and ~1200 μm), were used in this study. The materials were seeded with human osteoblastic (MG63) and fibroblastic (M-228 F01 and M-191 F01) cell lines. The cells were visualized by two techniques, scanning electron microscopy and confocal microscopy. For confocal microscopy cell nuclei were labeled with propidium iodide (IP) and the extracellular matrix components (type I collagen and osteocalcin) by specific antibodies. Cells and matrix were visualized by fluorescence. The bioactive glass used in this study was shown to be non cytotoxic. Cell growth and colonization at the surface and in the depth of the material were observed. Extracellular matrix deposition was also demonstrated which proved the proper biofunctionality of the biomaterial. Scanning electron microscope allowed us to visualize cells at a high magnification at the surface of the bioglass and evidenced that the biomaterials were covered by a sheet of cells with their matrix; on the other hand, confocal microscopy permitted us to observe cell ingrowth and matrix deposition within the depth of the substitute. We showed that extracellular matrix was synthesized mainly in the upper levels where the cell population was the most confluent. In summary, this porous bioglass appears promising for bone substitution.
机译:这项研究的目的是评估一种新开发的多孔生物活性玻璃作为骨替代物的细胞相容性,细胞向内生长和细胞外基质沉积。本研究使用了两种类型的生物活性玻璃,它们的孔径不同(75和20 ppi,分别为〜350和〜1200μm)。将材料接种人成骨细胞(MG63)和成纤维细胞(M-228 F01和M-191 F01)细胞系。通过两种技术使细胞可视化,扫描电子显微镜和共聚焦显微镜。对于共聚焦显微镜,通过特异性抗体用碘化丙锭(IP)和细胞外基质成分(I型胶原和骨钙蛋白)标记细胞核。通过荧光观察细胞和基质。这项研究中使用的生物活性玻璃被证明是无细胞毒性的。观察到细胞在材料表面和深度的生长和定植。还证明了细胞外基质沉积,证明了该生物材料的适当生物功能。扫描电子显微镜使我们能够以高放大倍率观察生物玻璃表面的细胞,并证明生物材料被一片带有其基质的细胞覆盖。另一方面,共聚焦显微镜使我们能够观察到替代物深度内的细胞向内生长和基质沉积。我们表明,细胞外基质主要在细胞群体最汇合的较高水平合成。总而言之,这种多孔生物玻璃似乎有望用于骨替代。

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