首页> 外文期刊>Journal of biomedical materials research. Part B, Applied biomaterials. >Effect of cartilaginous matrix components on the chondrogenesis and hypertrophy of mesenchymal stem cells in hyaluronic acid hydrogels
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Effect of cartilaginous matrix components on the chondrogenesis and hypertrophy of mesenchymal stem cells in hyaluronic acid hydrogels

机译:软骨基质组分对透明质酸水凝胶中间充质干细胞软骨发生及肥大的影响

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ABSTRACT The microenvironment of the extracellular matrix (ECM) plays a key role in directing the viability and subsequent differentiation of the encapsulated stem cells by the specific integration between the hydrated biomolecules and cell surface receptors. Herein, we developed a hydrogel platform based on hyaluronic acid (HA) that presents cartilage ECM molecules as a form of developmental cues. The hybrid hydrogels were generated by coupling photo‐cross‐linkable methacrylated HA (MeHA) with selected cartilaginous ECM molecules including chondroitin sulfate (CS) and type I collagen (Col I), and we studied the decoupled function of these cues in regulating the initial chondrogenesis, subsequent hypertrophy, and tissue mineralization by hMSCs. The results indicate upregulated mRNA expression of the chondrogenesis markers in the HA hydrogels that contain Col I or CS, and decreased expression of the hypertrophic markers compared with the control MeHA group. The quantification results also show that glycosaminoglycans accumulation increases in the hybrid hydrogels containing cartilaginous ECM molecules, both in vitro and in vivo . We hypothesize that these additional ECM components in the HA hydrogels further regulate the hMSCs chondrogenesis and hypertrophy by coordination. The understanding obtained in this study may guide biomaterial scaffold design, thereby facilitating manipulation of the differentiation and mineralization of induced hMSCs for application in the repair of different musculoskeletal defects. ? 2016 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 105B: 2292–2300, 2017.
机译:摘要细胞外基质(ECM)的微环境在引导封装的干细胞通过水合生物分子和细胞表面受体之间的特定积分来引导封装的干细胞的分化起到关键作用。在此,我们开发了一种基于透明质酸(HA)的水凝胶平台,其呈现出软骨ECM分子作为一种发育线索。通过在包括软骨素(CS)和I型胶原(COL I)的选定的软骨ECM分子中通过偶联光交联的甲基丙烯酸甲酸HA(MEHA)产生杂种水凝胶。我们研究了这些提示的解耦功能来调节初始HMSCs的软骨发生,随后的肥大和组织矿化。结果表明,与对照Meha组相比,含有Col I或Cs的HA水凝胶中的软骨发生标记物的上调MRNA表达,并降低了肥厚标记物的表达。定量结果还表明,在体外和体内含有软骨内ECM分子的杂种水凝胶中的糖胺聚糖累积增加。我们假设HA水凝胶中的这些额外的ECM组分进一步调节HMSCs软骨发生和通过协调的肥大。本研究中获得的理解可引导生物材料支架设计,从而促进诱导HMSCs的分化和矿化以在修复不同肌肉骨骼缺陷的修复中的应用。还2016 Wiley期刊,Inc.J生物保解员B:Appl Biomater,105B:2292-2300,2017。

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