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首页> 外文期刊>Clinical oral implants research >Osteoblastic and osteoclastic differentiation on SLA and hydrophilic modified SLA titanium surfaces
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Osteoblastic and osteoclastic differentiation on SLA and hydrophilic modified SLA titanium surfaces

机译:SLA和亲水改性SLA钛表面的成骨和破骨细胞分化

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摘要

Purpose: We evaluated the activities of both osteoblastic and osteoclastic differentiation on sandblasted/acid etched (SLA), hydrophilic SLA surfaces (modSLA) and pretreatment titanium (PT). Material and methods: The osteoblastic differentiation was evaluated by alkaline phosphatase analysis and Alizarin Red S staining, and the expression of bone-related proteins, alkaline phosphatase (ALP), runt-related transcription factor 2 (Runx2), osteopontin (OPN), and osteocalcin (OCN), was investigated by reverse transcriptase-polymerase chain reaction (RT-PCR). Primary mice monocytes were expanded and differentiated in the presence of macrophage-colony stimulating factor (M-CSF), and osteoclastic differentiation was evaluated by actin ring formation assay and tartrate-resistant acid phosphatase (TRAP) activity assay. Real-time PCR tests were performed to investigate the expression of gene mRNA expression levels in osteoclast cells. Result: Differentiation of osteoblasts in the Alizarin Red S test staining and ALP assay was significantly increased in the modSLA surface. The preceding results were supported by the result of RT-PCR for the expression of Runx2, OPN, and OCN. As for osteoclastic activity, differentiated osteoclasts rarely existed on the SLA and modSLA surface with actin ring. The results of real-time PCR and TRAP activity supported the preceding results. Conclusion: It may be concluded that the modSLA surface promotes osteogenic effect and prevents osteoclastic differentiation. Promotion of osteoblastic proliferation after a short-term cell culture might be responsible for stimulated bone regeneration implying that early loading may be possible. Also, the anti-osteoclastic effect of the modSLA surface may contribute to maintenance of the marginal bone level of dental implants, implying long-term stability would be provided by this surface technology. The modSLA surface may not only make early loading possible but possibly reduce marginal bone loss during the maintenance phase.
机译:目的:我们评估了喷砂/酸蚀(SLA),亲水性SLA表面(modSLA)和预处理钛(PT)上成骨和破骨细胞分化的活性。材料和方法:通过碱性磷酸酶分析和茜素红S染色评估成骨细胞的分化,并评估骨相关蛋白,碱性磷酸酶(ALP),矮子相关转录因子2(Runx2),骨桥蛋白(OPN)和骨相关蛋白的表达。通过逆转录聚合酶链反应(RT-PCR)研究了骨钙素(OCN)。在巨噬细胞集落刺激因子(M-CSF)存在下,原代小鼠单核细胞扩增并分化,并通过肌动蛋白环形成分析和抗酒石酸酸性磷酸酶(TRAP)活性评估破骨细胞的分化。进行实时PCR测试以研究破骨细胞中基因mRNA表达水平的表达。结果:在modSLA表面,茜素红S检验染色和ALP分析中成骨细胞的分化显着增加。先前的结果得到RT-PCR对Runx2,OPN和OCN表达的支持。至于破骨细胞活性,在具有肌动蛋白环的SLA和modSLA表面上很少存在分化的破骨细胞。实时PCR和TRAP活性的结果支持上述结果。结论:可以得出结论,modSLA表面可促进成骨作用并防止破骨细胞分化。短期细胞培养后促进成骨细胞增殖可能是刺激骨再生的原因,这意味着可能早期加载。另外,modSLA表面的抗破骨作用可能有助于维持牙科植入物的边缘骨水平,这意味着该表面技术将提供长期稳定性。 modSLA表面不仅可以使早期加载成为可能,而且可以减少维护阶段的边缘性骨丢失。

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