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3D chitosan–gelatin–chondroitin porous scaffold improves osteogenic differentiation of mesenchymal stem cells

机译:3D壳聚糖-明胶-软骨素多孔支架可改善间充质干细胞的成骨分化

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摘要

A porous 3D scaffold was developed to support and enhance the differentiation process of mesenchymal stem cells (MSC) into osteoblasts in vitro. The 3D scaffold was made with chitosan, gelatin and chondroitin and it was crosslinked by EDAC. The scaffold physicochemical properties were evaluated. SEM revealed the high porosity and interconnection of pores in the scaffold; rheological measurements show that the scaffold exhibits a characteristic behavior of strong gels. The elastic modulus found in compressive tests of the crosslinked scaffold was about 50 times higher than the non-crosslinked one. After 21 days, the 3D matrix submitted to hydrolytic degradation loses above 40% of its weight. MSC were collected from rat bone marrow and seeded in chitosan–gelatin–chondroitin 3D scaffolds and in 2D culture plates as well. MSC were differentiated into osteoblasts for 21 days. Cell proliferation and alkaline phosphatase activity were followed weekly during the osteogenic process. The osteogenic differentiation of MSC was improved in 3D culture as shown by MTT assay and alkaline phosphatase activity. On the 21st day, bone markers, osteopontin and osteocalcin, were detected by the PCR analysis. This study shows that the chitosan–gelatin–chondroitin 3D structure provides a good environment for the osteogenic process and enhances cellular proliferation.
机译:开发了一种多孔3D支架,以支持和增强间充质干细胞(MSC)体外分化为成骨细胞的过程。 3D支架由壳聚糖,明胶和软骨素制成,并通过EDAC交联。评价支架的理化性质。 SEM显示支架中的高孔隙率和孔的互连性;流变学测量表明该支架表现出强凝胶的特征行为。在交联支架的压缩测试中发现的弹性模量比未交联的支架高约50倍。 21天后,经受水解降解的3D基质的重量损失超过40%。从大鼠骨髓中收集MSC,并接种在壳聚糖-明胶-软骨素3D支架和2D培养板中。将MSC分化为成骨细胞21天。成骨过程中每周进行一次细胞增殖和碱性磷酸酶活性的监测。 MTT分析和碱性磷酸酶活性显示,在3D培养中,MSC的成骨分化得到改善。在第21天,通过PCR分析检测了骨标志物骨桥蛋白和骨钙蛋白。这项研究表明,壳聚糖-明胶-软骨素3D结构为成骨过程提供了良好的环境,并增强了细胞增殖。

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