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首页> 外文期刊>Dental traumatology: official publication of International Association for Dental Traumatology >Human periodontal ligament cells reaction on a novel hydroxyapatite-collagen scaffold
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Human periodontal ligament cells reaction on a novel hydroxyapatite-collagen scaffold

机译:人牙周膜细胞在新型羟基磷灰石-胶原支架上的反应

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Background: Periodontal tissue regeneration presents a highly promising method for restoring periodontal structures. The development of a suitable bioactive scaffold that promotes cell proliferation and differentiation is critical in periodontal tissue engineering. The aim of this study was to evaluate the biocompatibility of a novel 3-dimensional hydroxyapatite-collagen scaffold with human periodontal ligament (hPDL) cell culture. Methods: The scaffold was produced from a natural collagen matrix - purified porcine acellular dermal matrix (PADM), which was then treated with hydroxyapatite (HA) through a biomimetic chemical process to obtain hydroxyapatite-porcine acellular dermal matrix (HA-PADM) scaffold. The hPDL cells were cultured with HA-PADM scaffolds for 1, 3, 6, 14, and 28 days. The cell viability assay, scanning electron microscopy (SEM), hematoxylin and eosin (H&E) staining, immunohistochemistry, and confocal microscopy were employed in different time points to evaluate the biocompatibility of the scaffolds with hPDL cells. Results: The cell viability assay (WST-1 test) verified cell proliferation on the HA-PADM scaffolds. The SEM study showed unique morphology of hPDL cells, which attach and spread on the surface of the scaffolds. The H&E staining, immunohistochemistry, and confocal microscopy demonstrated that hPDL cells were able to grow into the HA-PADM scaffolds and maintain viability after prolonged culture. Conclusions: This study proved that HA-PADM scaffold is -biocompatible for hPDL cells. The cells were able to proliferate and migrate into the scaffold. These observations suggest that HA-PADM is a potential cell carrier for periodontal tissue regeneration.
机译:背景:牙周组织再生是恢复牙周结构的一种很有前途的方法。在牙周组织工程中,促进细胞增殖和分化的合适生物活性支架的开发至关重要。这项研究的目的是评估新型3维羟基磷灰石-胶原蛋白支架与人牙周膜(hPDL)细胞培养的生物相容性。方法:从天然胶原蛋白基质-纯化的猪脱细胞真皮基质(PADM)制备支架,然后通过仿生化学工艺用羟基磷灰石(HA)处理以获得羟基磷灰石-猪脱细胞真皮基质(HA-PADM)支架。用HA-PADM支架将hPDL细胞培养1、3、6、14和28天。在不同时间点使用细胞活力测定,扫描电子显微镜(SEM),苏木精和曙红(H&E)染色,免疫组化和共聚焦显微镜来评估支架与hPDL细胞的生物相容性。结果:细胞活力测定(WST-1测试)验证了HA-PADM支架上的细胞增殖。 SEM研究显示hPDL细胞的独特形态,该形态附着并散布在支架表面上。 H&E染色,免疫组织化学和共聚焦显微镜表明,hPDL细胞能够长成HA-PADM支架并在长时间培养后保持活力。结论:该研究证明HA-PADM支架对于hPDL细胞具有生物相容性。细胞能够增殖并迁移到支架中。这些观察结果表明HA-PADM是牙周组织再生的潜在细胞载体。

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