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作 者:林志立[1] 梁建平[1] 庄秀妹[2] LIN Zhili;LIANG Jianping;ZHUANG Xiumei(Department of Stomatology,Guangzhou First People's Hospital,Guangzhou 510180,Guangdong Province,China)
机构地区:[1]广州市第一人民医院口腔科,广东广州510180 [2]中山大学附属孙逸仙纪念医院口腔科,广东广州510180
出 处:《中国口腔种植学杂志》2018年第3期101-104,共4页Chinese Journal of Oral Implantology
基 金:国家自然科学基金青年基金项目(81600899)
摘 要:目的:探讨亲水性钛表面微纳米形貌对人牙周膜成纤维细胞(periodontal ligament cells, PDLCs)增殖与成骨分化的影响。方法:前期已通过阳极氧化法和喷砂碱热法构建相似微纳米形貌,但显示不同亲水性的钛表面,两组钛片表面接种PDLCs,采用CCK8法在培养1、4、7、14天时检测PDLCs细胞活性;第7天和14天时检测总蛋白浓度与碱性磷酸酶(ALP)活性,并在第7天时检测成骨标志物ALP、I型胶原(COL1)与成骨特异性转录因子2 (RUNX2)的mRNA表达水平。采用SPSS13.0软件包对数据进行统计学分析。结果:相比阳极氧化组,亲水性更强的喷砂碱热组PDLCs在接种4、7、14天后细胞活性更高;培养7、14天后,喷砂碱热组PDLCs的总蛋白浓度、ALP活性均高于阳极氧化组;第7天时,喷砂碱热组PDLCs中ALP、COL1与RUNX2的mRNA表达水平均高于阳极氧化组。结论:喷砂碱热组钛表面微纳米形貌较阳极氧化组显著促进PDLCs增殖与成骨分化,该过程可能与其良好的亲水性有关。Objective: To investigate the effect of hydrophilicity of titanium with micro/nanotopographical surface on the cell viability and osteogenic differentiation in human periodontal ligament cells(PDLCs).Methods: Methods of anodic oxidation and sandblast-alkali heat were utilized to establish scale structures. PDLCs were seeded on these two titanium discs, cell viability was detected at 1, 4, 7 and 14 days by CCK8 assay. Total protein values and alkaline phosphatase(ALP) activity were examined at 7 and 14 days. ALP, collagen-I(COL1) and runt related transcription factor 2(RUNX2) m RNA expression at 7 days were detected by qRT-PCR. The date was statistically analyzed with SPSS13.0 software package.Results: Compared with anodic oxidation surfaces, PDLCs on the sandblast-alkali heat surface discs with well hydrophilicity exhibited enhanced cell viability, increased total protein values, up-regulated ALP activity and overexpression of ALP, COL1 and RUNX2 levels. Conclusion: Micro-nanotopographical surface of titanium implant in sandblast-alkali heat group promotes cell viability and osteogenic differentiation of PDLCs, which may be affected by its hydrophilicity.
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