Moon Kyung-Suk, Choi Eun-Joo, Oh Seunghan, Kim Sungtae
Department of Dental Biomaterials and Institute of Biomaterial and Implant, College of Dentistry, Wonkwang University, Iksan, Jeonbuk 570-749, Republic of Korea.
Department of Oral and Maxillofacial Surgery, College of Dentistry, Wonkwang University, Iksan, Jeonbuk 570-749, Republic of Korea.
Biomed Res Int. 2015;2015:742192. doi: 10.1155/2015/742192. Epub 2015 Sep 7.
The purpose of this research was to covalently graft fibroblast growth factor 2 (FGF-2) onto biphasic calcium phosphate (BCP) via a bifunctional cross-linker technique and to estimate the optimal dose of FGF-2 resulting in the best osteogenic differentiation of human mesenchymal stem cells (hMSCs). SEM observation revealed that the surface of the 100 ng FGF-2 coated BCP was completely covered with the nanoparticles expected to be from the silane coupling agent. XRD, FT-IR, and XPS analysis showed that silane treatment, bifunctional cross-linker coating, and FGF-2 covalent grafts were conducted successfully without deforming the crystalline structure of BCP. An MTT assay demonstrated that FGF-2 coated BCP had good biocompatibility, regardless of the concentration of FGF-2, after 24 or 48 h of incubation. An alkaline phosphatase (ALP) activity assay (14 days of incubation) and the ALP gene expression level of real-time PCR analysis (7 days of incubation) revealed that 50, 100, and 200 ng FGF-2 coated BCP induced the highest activities among all experimental groups and control group (P < 0.05). Thus, low concentrations of FGF-2 facilitated excellent osteogenesis and were effective at enhancing osteogenic potential. Also, the bifunctional cross-linker technique is expected to be a more feasible way to induce osteogenic differentiation while minimizing the risk of FGF-2 overdose.
本研究的目的是通过双功能交联剂技术将成纤维细胞生长因子2(FGF-2)共价接枝到双相磷酸钙(BCP)上,并评估能使人骨髓间充质干细胞(hMSCs)实现最佳成骨分化的FGF-2最佳剂量。扫描电子显微镜(SEM)观察显示,涂覆100 ng FGF-2的BCP表面完全被预期来自硅烷偶联剂的纳米颗粒覆盖。X射线衍射(XRD)、傅里叶变换红外光谱(FT-IR)和X射线光电子能谱(XPS)分析表明,硅烷处理、双功能交联剂涂覆和FGF-2共价接枝均成功进行,且未使BCP的晶体结构变形。噻唑蓝(MTT)比色法表明,孵育24或48小时后,无论FGF-2浓度如何,涂覆FGF-2的BCP均具有良好的生物相容性。碱性磷酸酶(ALP)活性测定(孵育14天)和实时聚合酶链反应(PCR)分析的ALP基因表达水平(孵育7天)显示,涂覆50、100和200 ng FGF-2的BCP在所有实验组和对照组中诱导的活性最高(P < 0.05)。因此,低浓度的FGF-2促进了良好的成骨作用,并有效地增强了成骨潜能。此外,双功能交联剂技术有望成为一种更可行的诱导成骨分化的方法,同时将FGF-2过量的风险降至最低。