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首页> 外文期刊>Calcified tissue international. >Effects of roughness, fibronectin and vitronectin on attachment, spreading, and proliferation of human osteoblast-like cells (Saos-2) on titanium surfaces.
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Effects of roughness, fibronectin and vitronectin on attachment, spreading, and proliferation of human osteoblast-like cells (Saos-2) on titanium surfaces.

机译:粗糙度,纤连蛋白和玻连蛋白对钛表面上人成骨样细胞(Saos-2)附着,扩散和增殖的影响。

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摘要

The influence of surface roughness and the presence of adhesion molecules in the culture medium were studied regarding cell adhesion, shape, and proliferation of osteoblast-like cells grown on two types of titanium disk. Type I disks were acid etched and type II disks were sandblasted and acid etched. Surface roughness was determined by contact profilometry and scanning electron microscopy. Chemical composition and oxide thickness of the superficial titanium layer were established with energy dispersive X-ray spectrometry, electron spectroscopy for chemical analysis and auger electron spectroscopy. Titanium release in the culture medium was assessed by inductively coupled plasma-optical emission spectrometry. Osteoblast-like cells (Saos-2) were cultured on both types of titanium disks (1) in standard conditions (DMEM culture medium supplemented with fetal calf serum), (FCS), (2) with the culture medium alone (DMEM alone), (3) in the presence of fibronectin or vitronectin (DMEM supplemented with fibronectin or vitronectin). Cultures were also performed in the presence of monoclonal anti-integrin (beta1, alphav) to test the cell adhesion molecules involved in the cell binding to the titanium surface. We found that sandblasting does not modify the chemical surface composition and that titanium represents only 5-6% (in the atom percentage) of surface elements. Release of titanium in the culture medium was found to increase from 24 to 72 hours. In the absence of FCS, fibronectin, or vitronectin, cells appeared scanty and packed in clusters. On the contrary, cells cultured in the presence of FCS, fibronectin, or vitronectin were flattened with large and thin cytoplasmic expansions. The addition of anti beta1 or alphav integrin subunit monoclonal antibody in the culture medium decreased adhesion and spreading of cells, particularly in the presence of fibronectin. Cell proliferation was significantly higher on culture plastic than on both types of disks, but was increased on rough but not on smooth surfaces. These results indicate that a high surface roughness and presence of fibronectin or vitronectin are critical elements for adhesion, spreading, and proliferation of cells on titanium surfaces.
机译:研究了表面粗糙度和培养基中粘附分子的存在对在两种类型的钛盘上生长的成骨样细胞的细胞粘附,形状和增殖的影响。对I型圆盘进行酸蚀,对II型圆盘进行喷砂和酸蚀。通过接触轮廓仪和扫描电子显微镜确定表面粗糙度。利用能量色散X射线能谱,化学分析用电子能谱和俄歇电子能谱仪建立了表面钛层的化学成分和氧化物厚度。通过电感耦合等离子体发射光谱法评估培养基中钛的释放。将成骨细胞样细胞(Saos-2)在两种类型的钛圆片上(1)在标准条件下(DMEM培养基补充胎牛血清),(FCS),(2)和单独的培养基(仅DMEM)培养,(3)在纤连蛋白或玻连蛋白(DMEM补充有纤连蛋白或玻连蛋白)的存在下。在单克隆抗整合素(β1,αv)存在下也进行培养,以测试参与细胞与钛表面结合的细胞粘附分子。我们发现喷砂不会改变化学表面成分,钛仅占表面元素的5-6%(原子百分比)。发现钛在培养基中的释放从24小时增加到72小时。在不存在FCS,纤连蛋白或玻连蛋白的情况下,细胞显得稀少并且聚集成簇。相反,在FCS,纤连蛋白或玻连蛋白存在下培养的细胞被扁平化,具有大而薄的胞质扩展。在培养基中添加抗beta1或alphav整合素亚基单克隆抗体会降低细胞的黏附和扩散,特别是在存在纤连蛋白的情况下。在培养塑料上,细胞增殖显着高于两种类型的磁盘,但在粗糙的表面上却增加,但在光滑的表面上则没有。这些结果表明,高表面粗糙度和纤连蛋白或玻连蛋白的存在是钛表面上细胞粘附,扩散和增殖的关键因素。

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