Aybar Buket, Emes Yusuf, Atalay Belir, Tanrikulu Sinasi, Kaya A Selhan, Işsever Halim, Ceyhan Taşkin, Bilir Ayhan
Department of Oral Surgery, School of Dentistry, Istanbul University, Istanbul, Turkey.
Implant Dent. 2009 Feb;18(1):75-85. doi: 10.1097/ID.0b013e31818c5bd8.
The goal of this present study was to evaluate the behavior of neonatal rat calvarial osteoblast-like cells cultured on different implant surfaces.
Sandblasted acid-etched (SLA) surfaces of 2 different companies with different alloy properties were used. These were named as SLA-1 and SLA-2. The osteoblasts behavior were analyzed on sand blasted-acid etched (SLA-1) surface (Straumann, Basel, Switzerland), sand blasted-acid etched (SLA-2) surface (Alpha bio, Petach-tikva, Israel), acid-etched surface (Alpha bio), machined surface (Alpha bio). To analyze the effect of titanium surfaces on cell proliferation, cell numbers, and cell viability cells were cultured on titanium discs for 7 days and measurements were held out at 24 hours and on day 7. Cell proliferation rate was assessed by bromodeoxyuridine (BrdU) immunohistochemical technique. Cell morphologies were evaluated by scanning electron microscopy.
The highest number of BrdU labeled cells were seen on SLA-1 group at the end of 24 hours. The number of cells was found to be the highest in the acid-etched group on the 7th day, even though there were no significant differences between the groups at the end of 24 hours. Scanning electron microscopy views showed the morphological differences between the groups. Osteoblasts were able to proliferate on all of the tested surfaces, with differences in cell count and DNA synthesis values between the groups.
Implant surface characteristics may modulate the biological response of osteoblast-like cells depending on the manufacturing techniques and cell culturing procedures.
本研究的目的是评估在不同种植体表面培养的新生大鼠颅骨成骨样细胞的行为。
使用了具有不同合金特性的2家不同公司的喷砂酸蚀(SLA)表面。这些分别命名为SLA - 1和SLA - 2。在喷砂酸蚀(SLA - 1)表面(瑞士巴塞尔的士卓曼公司)、喷砂酸蚀(SLA - 2)表面(以色列佩塔提克瓦的阿尔法生物公司)、酸蚀表面(阿尔法生物公司)、机械加工表面(阿尔法生物公司)上分析成骨细胞行为。为了分析钛表面对细胞增殖、细胞数量和细胞活力的影响,将细胞在钛盘上培养7天,并在24小时和第7天进行测量。通过溴脱氧尿苷(BrdU)免疫组织化学技术评估细胞增殖率。通过扫描电子显微镜评估细胞形态。
在24小时结束时,SLA - 1组中可见BrdU标记细胞数量最多。在第7天,酸蚀组中的细胞数量最高,尽管在24小时结束时各组之间没有显著差异。扫描电子显微镜观察显示了各组之间的形态差异。成骨细胞能够在所有测试表面上增殖,各组之间在细胞计数和DNA合成值方面存在差异。
种植体表面特性可能根据制造技术和细胞培养程序调节成骨样细胞的生物学反应。