a Department of Prosthodontics , Oral Science Research Center, Yonsei University College of Dentistry , Seoul , Korea.
b BK21 PLUS Project , Yonsei University College of Dentistry , Seoul , Korea.
J Biomater Sci Polym Ed. 2018 May-Jun;29(7-9):825-843. doi: 10.1080/09205063.2017.1354676. Epub 2017 Aug 2.
The purposes of this study are to confirm the role of Fibroblast Growth Factor-2 (FGF-2) in bone regeneration by adding various concentrations of FGF-2 to the collagen membrane and applying it to the Biphasic Calcium Phosphate (BCP) bone graft site for guided bone regeneration, to explore the potential of collagen membrane as FGF-2 carrier, and to determine the optimum FGF concentration for enhancement of bone regeneration. Four bone defects of 8 mm in diameter were created in 18 New Zealand rabbit calvaria. After BCP bone graft, graft material was covered with collagen membranes adding various concentration of FGF-2. The concentration of FGF-2 was set at 1.0, 0.5, 0.1 mg/ml, and same amount of saline was used in the control group. To confirm the bone regeneration over time, six New Zealand rabbits were sacrificed each at 2, 4, and 12 weeks, and the amounts of new bone and residual bone graft material were analyzed by histologic and histomorphometric analysis. Qualitative analyses are also conducted through immunohistochemistry, Tetrate-resistant acid phosphatase (TRAP) stain and Russell-Movat pentachrome stain. As the healing period increased, the formation of new bone increased and the amount of residual graft material decreased in all experimental groups. Immunohistochemistry, TRAP staining and pentachrome staining further showed that the addition of FGF-2 promoted bone regeneration in all experimental groups. It was also confirmed that polymer collagen membrane can be used as a useful carrier of FGF-2 when enhanced early stage of new bone formation is required.
本研究旨在通过在胶原膜中添加不同浓度的成纤维细胞生长因子-2(FGF-2)并将其应用于双相磷酸钙(BCP)骨移植物部位进行引导性骨再生,以确认 FGF-2 在骨再生中的作用,探讨胶原膜作为 FGF-2 载体的潜力,并确定增强骨再生的最佳 FGF 浓度。在 18 只新西兰兔颅骨上创建了 4 个直径为 8mm 的骨缺损。在 BCP 骨移植后,用添加不同浓度 FGF-2 的胶原膜覆盖移植物材料。FGF-2 的浓度分别设定为 1.0、0.5 和 0.1mg/ml,对照组则使用等量的生理盐水。为了随时间确认骨再生,每组 6 只新西兰兔分别在 2、4 和 12 周时处死,通过组织学和组织形态计量学分析来分析新骨和残留骨移植物材料的量。还通过免疫组织化学、抗酒石酸酸性磷酸酶(TRAP)染色和 Russell-Movat 五重染色进行定性分析。随着愈合期的延长,所有实验组的新骨形成增加,残留移植物材料减少。免疫组织化学、TRAP 染色和五重染色进一步表明,在所有实验组中添加 FGF-2 都促进了骨再生。还证实了聚合物胶原膜在需要增强新骨形成的早期阶段时可以用作 FGF-2 的有用载体。