Cho Young-Dan, Kim Sung-Jun, Bae Han-Sol, Yoon Won-Joon, Kim Kyung-Hwa, Ryoo Hyun-Mo, Seol Yang-Jo, Lee Yong-Moo, Rhyu In-Chul, Ku Young
Department of Periodontology, School of Dentistry, Dental Research Institute, Seoul National University, Seou1 110-768, Republic of Korea.
Curr Pharm Des. 2016;22(30):4729-4735. doi: 10.2174/1381612822666160203143053.
Our previous studies demonstrated that a recombinant fibronectin (FN)-derived oligopeptide that we named F20 stimulated osteoblast adhesion, proliferation, and differentiation in vitro and in vivo. In the present study, we used a synthetic oligopeptide and investigated the osteogenic potential of F20 coating on titanium discs, to stimulate superior osseointegration for dental implant surface modification. Surface characteristic analysis of titanium was performed by confocal laser scanning microscopy (CLSM) observation. Synthetic F20 was coated onto the machined or SLA titanium discs by an adsorption procedure. ST2 cells were seeded on the titanium discs. We evaluated cell adhesion with SEM and CLSM observation, cell proliferation with picogreen assay, and osteoblast differentiation with real-time PCR, ALP activity assay, immunoblot assay and ALP staining. FITC-labeled F20 coating on the discs was detected by fluorescence, showing good F20 adsorption and different coating patterns according to the surface roughness. In the SEM and CLSM observations, cells were well attached on the machined surface and greater stress fiber formation was seen on discs coated with F20 than on other discs. F20 stimulated cellular proliferation, as well as osteoblast differentiation through the extracellular signalregulated kinase (Erk) signaling pathway. These cellular responses to F20 were slightly better on the machined titanium surface than the SLA surface. These results suggest that F20 promotes osteogenesis through the Erk pathway and is a suitable biomolecule for surface modification of dental implants for improved osseointegration.
我们之前的研究表明,一种我们命名为F20的重组纤连蛋白(FN)衍生寡肽在体外和体内均可刺激成骨细胞的黏附、增殖和分化。在本研究中,我们使用了一种合成寡肽,并研究了F20包被钛盘的成骨潜力,以刺激牙种植体表面改性后的骨整合。通过共聚焦激光扫描显微镜(CLSM)观察对钛进行表面特性分析。通过吸附程序将合成的F20包被在加工或SLA钛盘上。将ST2细胞接种在钛盘上。我们通过扫描电子显微镜(SEM)和CLSM观察评估细胞黏附,通过PicoGreen法评估细胞增殖,通过实时聚合酶链反应(PCR)、碱性磷酸酶(ALP)活性测定、免疫印迹测定和ALP染色评估成骨细胞分化。通过荧光检测盘上FITC标记的F20包被,显示出良好的F20吸附以及根据表面粗糙度不同的包被模式。在SEM和CLSM观察中,细胞在加工表面上附着良好,并且与其他盘相比,在F20包被的盘上观察到更大的应力纤维形成。F20通过细胞外信号调节激酶(Erk)信号通路刺激细胞增殖以及成骨细胞分化。这些对F20的细胞反应在加工钛表面上略优于SLA表面。这些结果表明,F20通过Erk途径促进骨生成,是用于改善骨整合的牙种植体表面改性的合适生物分子。