CaO-P2O5-MgO-SiO2-CaF体系玻璃陶瓷的基础研究。2. 培养细胞与玻璃陶瓷界面的超微结构研究。

Y Hara, Y Yoshimoto, T Abe, K Maeda, A Akamine, M Aono
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引用次数: 2

摘要

本研究的目的是确定玻璃陶瓷的生物相容性和培养细胞与玻璃陶瓷的粘附性。采用四种已建立的培养细胞系:人纤维肉瘤细胞(HT-1080)、人牙龈癌细胞(Ca9-22)、人骨肉瘤细胞(NY)和小鼠成骨细胞(MC3T3-E1)。为了进行相衬和电镜观察,它们被培养在玻璃陶瓷或聚苯乙烯盖作为对照的衬底上。所得结果如下:相衬显微镜显示,玻璃陶瓷既没有引起细胞变性,也没有引起细胞死亡。通过透射电镜观察,在衬底与Ca9-22之间以及玻璃陶瓷与NY之间的界面处观察到类似基层的非晶态结构。底物与MC3T3-E1之间有时存在类似的结构。而HT-1080则没有这种结构。结果表明,玻璃陶瓷具有良好的生物相容性。此外,从临床角度来看,关闭上皮细胞、纤维细胞和骨细胞的材料-组织界面似乎是可能的。
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[Basic studies on CaO-P2O5-MgO-SiO2-CaF system glass ceramics. 2. Ultrastructural study on interface between culture cells and glass ceramics].

The aim of this study was to determine biocompatibility of glass ceramics and adhesion of cultured cells to glass ceramics. Four established cultured cell lines, human fibrosarcoma cells (HT-1080), human gingival carcinoma cells (Ca9-22), human osteosarcoma cells (NY) and mouse osteoblasts (MC3T3-E1), were used. For phase-contrast and electron microscopic observation they were cultured on substrates of glass ceramics or polystyrene coverslips as a control. The results obtained were as follows. Glass ceramics caused neither cellular degeneration nor death, as revealed by phase-contrast microscopy. By transmission electron microscopy an amorphous structure similar to the basal lamina was observed at the interface between the substrates and Ca9-22, and between glass ceramics and NY. A similar structure sometimes existed between the substrates and MC3T3-E1. On the other hand HT-1080 showed no such structure. The findings suggest that the biocompatibility of glass ceramics was satisfactory. Furthermore, from the clinical point of view it seems to be possible to close the material-tissue interface with epithelial, fibrocytic and osteocytic cells.

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[Experimental studies on morphological changes of microvascular architecture following the free gingival autograft on denuded alveolar bone]. [A study of lipopolysaccharide derived from Bacteroides gingivalis]. [Distribution of enzymatically pathogenic bacteria from periodontal pocket in advancing periodontitis]. [The effect of superoxide dismutase on the inflammation induced by periodontal pathogenic bacteria and wound healing of gingival incision]. [Immunohistochemical localization of the chondroitin sulfate proteoglycan in demineralized rat periodontal tissue].
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