Sohn S-H, Jun H-K, Kim C-S, Kim K-N, Chung S-M, Shin S-W, Ryu J-J, Kim M-K
Department of Biochemistry, College of Medcine, Korea University, Seongbuk-Gu, Seoul, Korea.
J Oral Rehabil. 2006 Dec;33(12):898-911. doi: 10.1111/j.1365-2842.2006.01643.x.
Several features of the implant surface, such as roughness, topography and composition play a relevant role in implant integration with bone. This study was conducted in order to determine the effects of various thin layer hydroxyapatite (HA) coatings on anodized Ti surfaces on the biological responses of a human osteoblast-like cell line (MG63). MG63 cells were cultured on 100 nm HA (100 nm HA coating on anodized surface), 500-700 nm HA (500-700 nm HA coating on anodized surface), 1 mum HA (1 mum HA coating on anodized surface) and anodize (non-HA coating on anodized surface) Ti. The morphology of these cells was assessed by scanning electron microscopy (SEM). The cDNAs prepared from the total RNAs of the MG63 were hybridized into a human cDNA microarray (1152 elements). The appearances of the surfaces observed by SEM were different on each of the four dental substrate types. MG63 cells cultured on 100 nm HA, 1 mum HA and anodize exhibited cell-matrix interactions. It was 500-700 nm HA surface showing cell-cell interaction. In the expression of genes involved in osseointegration, several genes, including bone morphogenetic protein 2, latent transforming growth factor beta binding protein 1, catenin (cadherin-associated protein), integrin, PDGFRB and GDF-1 growth differentiation factor 1 were up-regulated on the different surfaces. Several genes, including fibroblast growth factor receptor 3, fibroblast growth factor 12 and CD4 were down-regulated on the different surfaces. The attachment and expression of key osteogenic regulatory genes were enhanced by the surface morphology of the dental materials used.
种植体表面的几个特征,如粗糙度、形貌和成分,在种植体与骨的整合中发挥着重要作用。进行这项研究是为了确定阳极氧化钛表面上各种薄层羟基磷灰石(HA)涂层对人成骨样细胞系(MG63)生物学反应的影响。MG63细胞在100nm HA(阳极氧化表面上的100nm HA涂层)、500 - 700nm HA(阳极氧化表面上的500 - 700nm HA涂层)、1μm HA(阳极氧化表面上的1μm HA涂层)和阳极氧化(阳极氧化表面上的非HA涂层)钛上培养。通过扫描电子显微镜(SEM)评估这些细胞的形态。从MG63的总RNA制备的cDNA与人类cDNA微阵列(1152个元件)杂交。在四种牙科基质类型中的每一种上,通过SEM观察到的表面外观都不同。在100nm HA、1μm HA和阳极氧化表面上培养的MG63细胞表现出细胞 - 基质相互作用。是500 - 700nm HA表面显示出细胞 - 细胞相互作用。在涉及骨整合的基因表达中,包括骨形态发生蛋白2、潜伏转化生长因子β结合蛋白1、连环蛋白(钙黏着蛋白相关蛋白)、整合素、血小板衍生生长因子受体β和生长分化因子1在内的几个基因在不同表面上上调。包括成纤维细胞生长因子受体3、成纤维细胞生长因子12和CD4在内的几个基因在不同表面上下调。所使用牙科材料的表面形态增强了关键成骨调节基因的附着和表达。