玻璃陶瓷的基础研究。3.体外对成骨细胞钙化的影响。

Y Yoshimoto, Y Hara, T Abe, S Miyatake, A Akamine, K Maeda, M Aono
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引用次数: 0

摘要

采用已建立的两种成骨细胞系(NY、MC 3 t3 - e1),体外测定玻璃陶瓷的生物相容性及其对成骨细胞初始钙化的影响。采用相衬显微镜和组织化学染色对细胞进行形态学观察。首先,将玻璃陶瓷颗粒置于60 mm的培养皿中,将细胞悬浮在添加10%胎牛血清(基础培养基)或添加50微克/毫升l -抗坏血酸的α - mem培养皿中。培养8 d或14 d后,采用von-Kossa染色法检测钙形成情况。偶氮染色法进行碱性磷酸酶染色。作为对照,在没有玻璃陶瓷颗粒的培养皿中同时染色。实验培养结果如下:1. 相衬显微镜显示,与玻璃陶瓷接触不会引起细胞死亡或变性。2. 在两种玻璃陶瓷细胞培养中,冯-科萨反应早在第8天就呈阳性。3.第8天碱性磷酸酶反应仅发生在mc3t3 - e1。反应局限于围绕玻璃陶瓷三维增殖的成纤维细胞和相对远离陶瓷的小多面体细胞。4. 第14天,MC 3 t3 - e 1在玻璃陶瓷周围形成大结节,von-Kossa染色均匀阳性。碱性磷酸酶阳性细胞呈辐条状。5. 在含有l -抗坏血酸的培养基中,NY的生长受到抑制,培养14天后,两种细胞的玻璃陶瓷周围都有丰富的von-Kossa阳性反应。在第8天的mc3t3 - e1中,玻璃陶瓷的碱性磷酸酶反应强于碱性培养基。相反,在两种细胞的对照培养中,在培养期间均出现阴性的von-Kossa反应。上述结果表明,玻璃陶瓷颗粒具有骨移植所需的生物相容性,促进了mc3t3 - e1在培养过程中的钙化。
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[Basic studies on glass ceramics. 3. Influence on calcification of osteogenic cells in vitro].

Two established osteogenic cell lines (NY, MC 3 T3-E 1) were used in vitro to determine the biocompatibility of glass ceramics and their effect on initial calcification of osteogenic cells. Morphological study of the cell under the phase-contrast microscopy and histochemical staining were applied as follows. First, glass ceramic granules were placed in 60 mm dishes, and cells were suspended in the dishes in alpha-MEM supplemented with 10% FBS (basic medium) or medium with 50 micrograms/ml of L-ascorbic acid added. After 8 or 14 day of culturing, calcium formation was tested by von-Kossa's staining. Also, alkaline phosphatase staining was performed by the azo-dye method. As controls, cultures in dishes without glass ceramic granules were stained at the same time. The results obtained in the experimental culture were as follows. 1. Phase contrast microscopy showed that contacts with glass ceramics did not cause cellular death or degeneration. 2. In both cell cultures with the glass ceramics the von-Kossa reaction was positive as early as the 8th day. 3. The alkaline phosphatase reaction on the 8th day occurred only in MC 3 T3-E 1. The reaction was localized on fibroblastic cells which proliferated three-dimensionally around glass ceramics, and on small polyhedral cells situated relatively for apart from the ceramics. 4. On the 14th day, the MC 3 T 3-E 1 formed large nodules around the glass ceramics, and they were stained uniformly positive by von-Kossa's method. The alkaline phosphatase-positive cells extended spoke-like forms. 5. In medium with L-ascorbic acid, growth of NY was inhibited, After being cultured for 14 days, abundant von-Kossa positive reaction was found around glass ceramics in both cells. In MC 3 T 3-E1 on the 8th days, the alkaline phosphatase reaction was stronger with glass ceramics than with basic medium only. On the contrary, in the control cultures of both cells there was negative von-Kossa reaction during the culture period. The above results showed that glass ceramic granules have the biocompatibility needed for bone grafts, and they facilitated calcification of MC 3 T 3-E 1 in culture.

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