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首页> 外文期刊>Artificial cells, nanomedicine, and biotechnology. >Differentiation of conjunctiva mesenchymal stem cells into secreting islet beta cells on plasma treated electrospun nanofibrous scaffold
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Differentiation of conjunctiva mesenchymal stem cells into secreting islet beta cells on plasma treated electrospun nanofibrous scaffold

机译:在血浆处理的电纺纳米纤维支架上,结膜间充质干细胞向分泌胰岛β细胞的分化

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Transplantation of stem cells using biocompatible nanofibrous scaffolds is a promising therapeutic method for treating Diabetic Mellitus. The aim of this study was to derive insulin-producing cells (IPCs) from conjunctiva-derived mesenchymal stem cell (CJMSCs) and to compare the functionality of differentiated IPCs in a three-dimensional (3D) culture with 2D. Furthermore, the effects of hydrophobicity of scaffold on IPCs differentiation were examined. Scanning electron microscopy (SEM), quantitative real times PCR (qPCR), Immunostaining and flow cytometry were used to analyze fabricated scaffold and the presence of IPCs. Functional maturity of differentiated cells was determined by measuring insulin release and the creation of IPCs was confirmed via gene and protein expression. In this study, the induced CJMSCs were morphologically similar to pancreatic islet-like cells. The expression of the islet-associated genes (glucagon, insulin and Pdx-1) and the insulin release (2.5-fold) in 3D-cultured cells was significantly higher than the 2D. The expression of IPCs genes was significantly higher in CJMSCs differentiated on plasma-treated nanofibers compared to those on untreated scaffolds. In conclusion, the results show that CJMSCs might be a new source for Diabetic Mellitus therapy and the nanofibrous scaffold could be used as a potential cell carrier for islet tissue engineering.
机译:使用生物相容性纳米纤维支架移植干细胞是治疗糖尿病的一种有前途的治疗方法。这项研究的目的是从结膜来源的间充质干细胞(CJMSCs)衍生出胰岛素产生细胞(IPC),并在二维(3D)培养和2D培养中比较分化IPC的功能。此外,检查了支架的疏水性对IPCs分化的影响。扫描电子显微镜(SEM),实时定量PCR(qPCR),免疫染色和流式细胞仪分析了制造的支架和IPC的存在。通过测量胰岛素释放来确定分化细胞的功能成熟度,并通过基因和蛋白质表达来确认IPC的产生。在这项研究中,诱导的CJMSCs在形态上类似于胰岛样细胞。与3D培养细胞相比,胰岛相关基因(胰高血糖素,胰岛素和Pdx-1)的表达和胰岛素释放(2.5倍)显着高于2D。与未经处理的支架相比,在经血浆处理的纳米纤维上分化的CJMSC中,IPCs基因的表达明显更高。总之,结果表明,CJMSCs可能是糖尿病治疗的新来源,并且纳米纤维支架可以用作胰岛组织工程的潜在细胞载体。

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