Yang Zhen, Liu Mingyue, Yang Yang, Zheng Miao, Yang Yang, Liu Xiaoqiang, Tan Jianguo
Department of Prosthodontics, Peking University School and Hospital of Stomatology, National Clinical Research Center for Oral Diseases, National Engineering Laboratory for Digital and Material Technology of Stomatology, Beijing Key Laboratory of Digital Stomatology Beijing 100081 P. R. China
First Clinical Division, Peking University School and Hospital of Stomatology Beijing 100034 P. R. China.
RSC Adv. 2020 Feb 10;10(11):6200-6212. doi: 10.1039/c9ra08575k. eCollection 2020 Feb 7.
Rapid soft tissue integration is essential for long-term dental implant success. Zirconia is increasingly used as an abutment material owing to its excellent aesthetic properties and biocompatibility; however, it is bioinert, and tissue integration is poor. We developed a feasible surface modification method, exploiting the reactivity of polydopamine (PDA) films to immobilize cell-adhesion peptides (Arg-Gly-Asp, RGD) onto zirconia abutment surfaces. Further, we evaluated the effect thereof on human gingival fibroblast (HGF) behavior and oral bacterial adhesion, which influence the peri-implant soft tissue seal. HGF responses to linear KGGRGDSP and cyclic RGDfK sequences were compared. PDA deposition and covalent coupling of RGD were verified by X-ray photoelectron spectroscopy and fluorescence microscopy. The biological behaviors of HGFs on the modified zirconia; , adhesion, spreading, proliferation, gene and protein expression, were elucidated. Biofunctionalization of zirconia with the adhesion peptides significantly enhanced the biological activities of HGFs. Cyclic RGD induced slightly improved cell attachment, spreading, and proliferation, but similar cell differentiation when compared to linear RGD peptides. To assess their antimicrobial properties, the different substrates were exposed to cultures of the early colonizer or the periodontal pathogen , and bacterial adhesion was evaluated by scanning electron microscopy and live/dead staining. PDA and PDA-RGD coatings decreased zirconia surface colonization by both bacterial species to similar extents. Thus, PDA-RGD-functionalized zirconia modulates specific HGF responses, while maintaining the antimicrobial activity of the PDA coating. The selective bio-interaction pattern of this surface modification holds great promise for improving soft-tissue integration around zirconia abutments in clinical applications.
快速的软组织整合对于牙科种植体的长期成功至关重要。由于其出色的美学性能和生物相容性,氧化锆越来越多地被用作基台材料;然而,它是生物惰性的,组织整合性较差。我们开发了一种可行的表面改性方法,利用聚多巴胺(PDA)膜的反应性将细胞粘附肽(精氨酸 - 甘氨酸 - 天冬氨酸,RGD)固定在氧化锆基台表面。此外,我们评估了其对人牙龈成纤维细胞(HGF)行为和口腔细菌粘附的影响,这些因素会影响种植体周围软组织封闭。比较了HGF对线性KGGRGDSP和环状RGDfK序列的反应。通过X射线光电子能谱和荧光显微镜验证了PDA沉积和RGD的共价偶联。阐明了HGF在改性氧化锆上的生物学行为,包括粘附、铺展、增殖、基因和蛋白质表达。用粘附肽对氧化锆进行生物功能化显著增强了HGF的生物学活性。与线性RGD肽相比,环状RGD诱导细胞附着、铺展和增殖略有改善,但细胞分化相似。为了评估它们的抗菌性能,将不同的底物暴露于早期定植菌或牙周病原体的培养物中,并通过扫描电子显微镜和活/死染色评估细菌粘附。PDA和PDA - RGD涂层在相似程度上降低了两种细菌在氧化锆表面的定植。因此,PDA - RGD功能化的氧化锆调节特定的HGF反应,同时保持PDA涂层的抗菌活性。这种表面改性的选择性生物相互作用模式在临床应用中对于改善氧化锆基台周围的软组织整合具有很大的前景。