首页> 外文期刊>Journal of Endodontics: Official Journal of American Association of Endodontists >Effects of 3-dimensional Bioprinting Alginate/Gelatin Hydrogel Scaffold Extract on Proliferation and Differentiation of Human Dental Pulp Stem Cells
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Effects of 3-dimensional Bioprinting Alginate/Gelatin Hydrogel Scaffold Extract on Proliferation and Differentiation of Human Dental Pulp Stem Cells

机译:三维生生物监测藻酸盐/明胶水凝胶支架提取物对人牙髓干细胞增殖和分化的影响

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Introduction: Alginate/gelatin hydrogel (Alg-Gel) scaffold has been applied in tissue engineering, but the research on its application in dental tissues regeneration is still lacking. We investigated the effect of this scaffold on human dental pulp stem cells (hDPSCs). Methods: hDPSCs were cultured in both Alg-Gel and 3D-printed Alg-Gel scaffolds. Cell growth and adhesion were compared using fluorescein isothiocyanate-phalloidin staining and scanning electron microscopic micrographs. Changes in the proliferation in hDPSCs cultured in the complete culture medium containing aqueous extracts of the Alg-Gel or 3D-printed Alg-Gel scaffolds were examined using Cell Counting Kit-8 assay and flow cytometry analysis. Cells were cultured in the mineralization medium containing aqueous extracts of the Alg-Gel or 3D-printed Alg-Gel scaffolds for 7 or 14 days, and the differentiation of cells was shown by alizarin red S staining and alkaline phosphatase staining. The messenger RNA and protein expression of mineralization-related genes were detected with real-time polymerase chain reaction and Western blotting. Elemental analysis was used to test the material extract composition. Results: More cells were grown and adhered to the 3D-printed Alg-Gel scaffolds than the Alg-Gel scaffolds. The aqueous extracts of 3D-printed scaffolds can promote cell proliferation, and compared with Alg-Gel scaffolds, the extracts of 3D-printed scaffolds were more effective. Compared with the negative control group, 3D-printed Alg-Gel scaffold and Alg-Gel scaffold aqueous extracts promoted osteogenic/odontoblastic differentiation of hDPSCs with the enhanced formation of bone-like nodules and the alkaline phosphatase staining. The expression of mineralization-related genes was also up-regulated. 3D-printed scaffold aqueous extract contained more calcium and phosphorus ions than the Alg-Gel scaffold. Conclusions: These findings suggest that compared with the Alg-Gel scaffold, 3D-printed Alg-Gel is more suitable for the growth of hDPSCs, and the scaffold extracts can better promote cell proliferation and differentiation.
机译:介绍:藻酸盐/明胶水凝胶(ALG-GEL)支架已应用于组织工程,但仍然缺乏对其在牙科组织中的应用的研究。我们调查了该支架对人牙髓干细胞(HDPSC)的影响。方法:HDPSC在ALG-GEL和3D印刷的ALG-GEL支架中培养。使用荧光素异硫氰酸盐 - 阴阳蛋白染色和扫描电子显微镜显微照片进行比较细胞生长和粘附性。使用细胞计数试剂盒测定和流式细胞术分析检查在含有ALG-GEL或3D印刷的ALG-GEL支架的完全培养基中培养的HDPSC中的增殖的变化。将细胞培养在含有Alg-GEL或3D印刷的ALG-GEL支架的含水提取物的矿化培养基中7或14天,并且通过茜素红S染色和碱性磷酸酶染色表示细胞的分化。用实时聚合酶链反应和蛋白质印迹检测矿化相关基因的信使RNA和蛋白表达。元素分析用于测试材料提取物组合物。结果:种植更多的细胞并粘附到3D印刷的ALG-GEL支架上,而不是ALG-GEL支架。 3D印刷支架的水性提取物可以促进细胞增殖,并与阿尔凝胶支架相比,3D印刷支架的提取物更有效。与阴性对照组相比,3D印刷的ALG-GEL支架和ALG-GEL支架水性提取物促进了HDPSC的骨质发生/ OdontoBolas弹性分化,并具有增强的骨状结节和碱性磷酸酶染色的形成。矿化相关基因的表达也上调。 3D印刷的支架含水提取物含有比Alg-Gel支架更多的钙和磷离子。结论:这些研究结果表明,与阿尔 - 凝胶支架相比,3D印刷的Alg-GEL更适合于HDPSC的生长,并且支架提取物可以更好地促进细胞增殖和分化。

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