Kokubu Eitoyo, Yoshinari Masao, Matsuzaka Kenichi, Inoue Takashi
Department of Clinical Pathophysiology and Oral Health Science Center, Tokyo Dental College, Mihama-ku, Chiba 261-8501, Japan.
J Biomed Mater Res A. 2009 Oct;91(1):69-75. doi: 10.1002/jbm.a.32201.
The aim of this study was to investigate the behavior of rat periodontal ligament (PDL) cells cultured on fibroblast growth factor-2 (FGF-2)-immobilized titanium surfaces treated by oxygen (O2) plasma. We used cell disks (15 mm in diameter), and 35-mm culture dishes sputter-coated with titanium. These were treated with oxygen plasma and dipped in FGF-2 solution. Immobilized FGF-2 was visualized with a confocal laser-scanning microscope, and its weight was calculated to be approximately 22.6 ng/cm(2) using a quartz crystal microbalance-dissipation apparatus. The PDL cells were obtained from rat incisors. Cells from fourth subculture were seeded onto the FGF-2-immobilized titanium surface. Proliferation ratio, alkaline phosphatase (ALP) activity, and expressions of type I collagen and vascular endothelial growth factor (VEGF) mRNAs were evaluated. Proliferation ratio and expressions of type I collagen and VEGF mRNAs were significantly higher, whereas ALP activity was significantly lower in FGF-2-immobilized cells than in control group (p < 0.05). These findings suggest that oxygen plasma modification can immobilize FGF-2 onto a titanium surface. Immobilized FGF-2, although inferior to culture medium with FGF-2, influenced the proliferation of PDL cells and might have promoted collagen and vascular synthesis.
本研究旨在探讨在经氧(O2)等离子体处理的、固定有碱性成纤维细胞生长因子-2(FGF-2)的钛表面上培养的大鼠牙周膜(PDL)细胞的行为。我们使用了细胞盘(直径15毫米)以及溅射涂覆有钛的35毫米培养皿。这些样本经氧等离子体处理后浸入FGF-2溶液中。用共聚焦激光扫描显微镜观察固定化的FGF-2,并使用石英晶体微天平耗散仪计算其重量,结果约为22.6纳克/平方厘米。PDL细胞取自大鼠切牙。将第四次传代培养的细胞接种到固定有FGF-2的钛表面上。评估细胞增殖率、碱性磷酸酶(ALP)活性以及I型胶原蛋白和血管内皮生长因子(VEGF)mRNA的表达。与对照组相比,固定有FGF-2的细胞的增殖率以及I型胶原蛋白和VEGF mRNA的表达显著更高,而ALP活性显著更低(p < 0.05)。这些发现表明,氧等离子体改性可将FGF-2固定到钛表面。固定化的FGF-2虽然不如含有FGF-2的培养基,但影响了PDL细胞的增殖,可能促进了胶原蛋白和血管的合成。