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Differential response of human gingival fibroblasts to titanium- and titanium-zirconium-modified surfaces

机译:人类牙龈成纤维细胞对钛和钛锆改性表面的差异反应

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Background and Objective: Gingival fibroblasts are responsible for the constant adaptation, wound healing and regeneration of gingival connective tissue. New titanium-zirconium (TiZr) abutment surfaces have been designed to improve soft tissue integration and reduce implant failure compared with titanium (Ti). The aim of the present study was first to characterize a primary human gingival fibroblast (HGF) model and secondly to evaluate their differential response to Ti and TiZr polished (P), machined (M) and machined + acid-etched (modMA) surfaces, respectively. Material and Methods: HGF were cultured on tissue culture plastic or on the different Ti and TiZr surfaces. Cell morphology was evaluated through confocal and scanning electron microscopy. A wound healing assay was performed to evaluate the capacity of HGF to close a scratch. The expression of genes was evaluated by real-time RT-PCR, addressing: (i) extracellular matrix organization and turnover; (ii) inflammation; (iii) cell adhesion and structure; and (iv) wound healing. Finally, cells on Ti/TiZr surfaces were immunostained with anti-ITGB3 antibodies to analyze integrin β3 production. Matrix metalloproteinase-1 (MMP1) and inhibitor of metallopeptidases-1 (TIMP1) production were analyzed by enzyme-linked immunosorbent assays. Results: On tissue culture plastic, HGF showed no differences between donors on cell proliferation and on the ability for wound closure; α-smooth muscle actin was overexpressed on scratched monolayers. The differentiation profile showed increased production of extracellular matrix components. Ti and TiZr showed similar biocompatibility with HGF. TiZr increased integrin-β3 mRNA and protein levels, compared with Ti. Cells on TiZr surfaces showed higher MMP1 protein than Ti surfaces, although similar TIMP1 protein production. In this in vitro experiment, P and M surfaces from both Ti and TiZr showed better HGF growth than modMA. Conclusion: Taking into account the better mechanical properties and bioactivity of TiZr compared with Ti, the results of the present study show that TiZr is a potential clinical candidate for soft tissue integration and implant success.
机译:背景与目的:牙龈成纤维细胞负责牙龈结缔组织的持续适应,伤口愈合和再生。与钛(Ti)相比,新设计的钛锆(TiZr)基台表面可改善软组织整合并减少植入失败。本研究的目的是首先表征人类主要的牙龈成纤维细胞(HGF)模型,其次评估其对Ti和TiZr抛光(P),机加工(M)和机加工+酸蚀(modMA)表面的不同响应,分别。材料和方法:HGF培养在组织培养塑料上或不同的Ti和TiZr表面上。通过共聚焦和扫描电子显微镜评估细胞形态。进行伤口愈合测定以评估HGF闭合划痕的能力。通过实时RT-PCR评估基因的表达,解决:(i)细胞外基质的组织和周转; (ii)炎症; (iii)细胞粘附和结构; (iv)伤口愈合。最后,用抗ITGB3抗体对Ti / TiZr表面的细胞进行免疫染色,以分析整联蛋白β3的产生。通过酶联免疫吸附试验分析了基质金属蛋白酶-1(MMP1)和金属肽酶-1(TIMP1)的产生。结果:在组织培养塑料上,HGF在供体之间在细胞增殖和伤口闭合能力上没有差异。 α-平滑肌肌动蛋白在划痕的单层细胞上过表达。分化谱显示细胞外基质成分的产生增加。 Ti和TiZr与HGF表现出相似的生物相容性。与Ti相比,TiZr增加了整联蛋白β3mRNA和蛋白质的水平。 TiZr表面的细胞显示出比Ti表面更高的MMP1蛋白,尽管TIMP1蛋白的产量相似。在这个体外实验中,Ti和TiZr的P和M表面都比modMA表现出更好的HGF生长。结论:考虑到TiZr的力学性能和生物活性均优于Ti,因此本研究结果表明TiZr是软组织整合和植入成功的潜在临床候选者。

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