Department of Oral Surgery, Faculty of Dentistry, Istanbul University, Istanbul, Turkey.
Int J Med Sci. 2011;8(7):584-93. doi: 10.7150/ijms.8.584. Epub 2011 Oct 4.
The goal of this study was to evaluate the behavior of neonatal rat calvarial osteoblast-like cells cultured on different implant surfaces and exposed once or three times to a 660-nm light-emitting diode (LED).
An LED with a 660-nm wavelength was applied once or three times to cultured cells on standard and modified sandblasted acid-etched surfaces (SLA and SLActive; Straumann, Basel, Switzerland). To analyze the effect of the LED on cell proliferation, numbers, and viability, cells were cultured on titanium discs, and measurements were taken after 72 h. Cell proliferation rates were assessed using a bromodeoxyuridine immunohistochemical technique. Cell morphologies were evaluated by scanning electron microscopy (SEM).
Osteoblast-like cells proliferated on all tested surfaces, with differences among groups in cell counts and DNA synthesis values. The application of one LED treatment caused a significant increase in cell count in the SLActive group in comparison with the SLA group (p = 0.001), whereas the application of three LED treatments caused a significant decrease in cell count in the SLA group compared with the SLActive group (p < 0.001). After 72 h, the number of cells was highest in the SLActive group exposed once to the LED.
One LED application in the SLActive group resulted in significantly increased cell numbers. However, these findings were not exactly compatible with the SEM findings, which demonstrated fewer cells and weak attachments between cells and to the surface. Thus, further studies using different LED application times are needed to clarify the reason for the increased number of cells that are apparently incapable of attaching to the titanium surfaces after 72 h.
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,并在 660nm 发光二极管(LED)下照射一次或三次。
波长为 660nm 的 LED 被应用于标准和改良喷砂酸蚀表面(SLA 和 SLActive;Straumann,巴塞尔,瑞士)上培养的细胞一次或三次。为了分析 LED 对细胞增殖、数量和活力的影响,将细胞培养在钛盘上,在 72 小时后进行测量。使用溴脱氧尿苷免疫组织化学技术评估细胞增殖率。通过扫描电子显微镜(SEM)评估细胞形态。
成骨样细胞在所有测试的表面上增殖,细胞计数和 DNA 合成值在组间存在差异。与 SLA 组相比,SLActive 组单次 LED 处理应用后细胞计数显著增加(p=0.001),而 SLA 组三次 LED 处理应用后细胞计数显著减少(p<0.001)。72 小时后,经 LED 照射一次的 SLActive 组细胞数量最多。
SLActive 组单次 LED 应用导致细胞数量显著增加。然而,这些发现与 SEM 结果不完全一致,SEM 结果显示细胞数量较少,细胞与表面之间的附着较弱。因此,需要进一步研究不同的 LED 应用时间,以阐明为什么在 72 小时后,细胞数量增加,但显然无法附着在钛表面上。