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首页> 外文期刊>Journal of biomedical materials research. Part B, Applied biomaterials. >Proliferation, differentiation, and calcification of preosteoblast-like MC3T3-E1 cells cultured onto noncrystalline calcium phosphate glass
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Proliferation, differentiation, and calcification of preosteoblast-like MC3T3-E1 cells cultured onto noncrystalline calcium phosphate glass

机译:培养在非晶磷酸钙玻璃上的成骨细胞样MC3T3-E1细胞的增殖,分化和钙化

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摘要

The purpose of this study was to investigate calcium phosphate glass as a potential biomaterial for hard tissue repair. We prepared calcium phosphate glass using the system CaO-CaF_2-P_2O_5-MgO-ZnO and cultured MC3T3-E1 cells onto the glass in alpha-MEM with beta-glycero-phosphatase and ascorbic acid. Proliferation of the cells was determined to evaluate the biocompatibility of the prepared calcium phosphate glass. The alkaline phosphatase activity was measured to examine the osteoblast differentiation. Mineralization was evaluated by staining the calcium precipitates with Alizarin red. Culture onto the calcium phosphate glass exhibited no significant influence on cell proliferation compared to the polystyrene chosen as a control in this experiment (p > 0.05). The alkaline phosphatase activity in the experimental group, however, was enhanced by the calcium phosphate glass significantly at 10-18 days after incubation than that of the control group (p < 0.05). The promotion of bone-like tissue formation by the calcium phosphate glass was observed after 7 days and thereafter. The results of the present study indicate that the prepared calcium phosphate glass affects osteogenesis by increasing calcification of the extracellular matrix.
机译:这项研究的目的是研究磷酸钙玻璃作为硬组织修复的潜在生物材料。我们使用CaO-CaF_2-P_2O_5-MgO-ZnO系统制备磷酸钙玻璃,并在含有β-甘油磷酸酶和抗坏血酸的alpha-MEM中将MC3T3-E1细胞培养到玻璃上。确定细胞的增殖以评估所制备的磷酸钙玻璃的生物相容性。测量碱性磷酸酶活性以检查成骨细胞的分化。通过用茜素红染色钙沉淀物来评估矿化作用。与在本实验中选择作为对照的聚苯乙烯相比,在磷酸钙玻璃上进行培养对细胞增殖没有显着影响(p> 0.05)。然而,在孵育后10-18天,磷酸钙玻璃比对照组明显增强了实验组的碱性磷酸酶活性(p <0.05)。 7天后及之后观察到由磷酸钙玻璃促进的类骨组织形成。本研究的结果表明,制备的磷酸钙玻璃通过增加细胞外基质的钙化影响成骨作用。

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