*Resident, Department of Oral Biology Implantology, São Leopoldo Mandic School of Dentistry, Campinas, Brazil. †Professor, Department of Cellular and Molecular Biology, São Leopoldo Mandic School of Dentistry, Campinas, Brazil.
Implant Dent. 2017 Jun;26(3):373-377. doi: 10.1097/ID.0000000000000543.
The goal from this in vitro study was to evaluate osteoblast protein expression of collagen type 1 (col 1) and osteopontin (OPN) on titanium surface treated with double etching compared with a zirconia implant surface.
Discs were selected on both surfaces with respective treatments. Mouse MC3T3-E1 osteoblastic cells were tested for cell viability using the MTT assay. Subsequently, the quantification of col 1 and OPN secreted by osteoblastic cells plated on different surfaces was evaluated by enzyme linked immunosorbent assay (ELISA).
Regarding the cell proliferation, statistical analysis showed no significant effect of surface-time interaction and viable cell count on the surfaces of titanium versus zirconia. No statistical differences between the surfaces of titanium and zirconia on cell viability was found. The zirconia surface expression of OPN was significantly higher, which occurred in all times. Furthermore, zirconia demonstrated significantly greater in col 1 expression in 48 and 96 hours compared with titanium.
In this study, the zirconia surface demonstrated OPN and col 1 expression significantly higher as compared with titanium.
本体外研究的目的是评估经双重蚀刻处理的钛表面与氧化锆种植体表面相比,成骨细胞蛋白Ⅰ型胶原(col 1)和骨桥蛋白(OPN)的表达。
分别在两种表面选择圆盘进行相应处理。使用 MTT 法检测小鼠 MC3T3-E1 成骨细胞的细胞活力。随后,通过酶联免疫吸附试验(ELISA)评估在不同表面培养的成骨细胞分泌的 col 1 和 OPN 的定量。
关于细胞增殖,统计分析显示表面-时间相互作用和活细胞计数对钛与氧化锆表面没有显著影响。在细胞活力方面,钛表面与氧化锆表面之间未发现统计学差异。OPN 在氧化锆表面的表达明显更高,所有时间点均如此。此外,与钛相比,氧化锆在 48 小时和 96 小时时 col 1 的表达显著更高。
在这项研究中,与钛相比,氧化锆表面的 OPN 和 col 1 表达明显更高。