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Enhanced hepatic differentiation of rat bone marrow-derived mesenchymal stem cells in spheroidal aggregate culture on a decellularized liver scaffold

机译:去细胞肝支架上球状聚集培养物中大鼠骨髓间充质干细胞的肝分化增强

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摘要

In the present study, we aimed to determine whether the combination of aggregate culture and decellularized liver scaffolds (DLSs) promoted the hepatic differentiation of murine bone marrow-derived mesenchymal stem cells (BM-MSCs) into high yields of mature hepatocytes in vitro. Four culturing methods for differentiation [single cell (2D), spheroids (3D), 2D + DLS and 3D + DLS] were studied. To determine the differentiation stages of the MSCs, RT-qPCR of the hepatocyte genes, immunostaining of hepatocyte markers, and functional analyses were all performed. Compared with the other groups, hepatocyte-like cells which differentiated from BM-MSC spheroids on extracellular matrix (ECM) exhibited more intensive staining of stored glycogen, an elevated level of urea biosynthesis and albumin secretion as well as the higher expression of hepatocyte-specific genes. Our results indicated that DLSs combined with spheroidal aggregate culture may be used as an effective method to facilitate the hepatic maturation of BM-MSCs and may have future applications in stem cell-based liver regenerative medicine.
机译:在本研究中,我们旨在确定聚集培养物和脱细胞肝支架(DLSs)的组合是否在体外促进了小鼠骨髓来源的间充质干细胞(BM-MSCs)肝分化为高产量的成熟肝细胞。研究了四种分化培养方法[单细胞(2D),球体(3D),2D + DLS和3D + DLS]。为了确定MSC的分化阶段,进行了肝细胞基因的RT-qPCR,肝细胞标志物的免疫染色和功能分析。与其他组相比,与细胞外基质(ECM)上的BM-MSC球状体分化的肝样细胞表现出更强的存储糖原染色,尿素生物合成和白蛋白分泌水平升高以及肝细胞特异性表达更高基因。我们的研究结果表明,DLSs与球体聚集培养相结合可作为促进BM-MSC肝成熟的有效方法,并且在基于干细胞的肝再生医学中可能具有未来的应用。

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