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Induced Human Bone Marrow Stromal Cells Differentiate into Neural Cells by bFGF and Cocultured with Olfactory Ensheathing Cells

机译:bFGF诱导人骨髓基质细胞分化为神经细胞,并与嗅鞘细胞共培养

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Bone marrow stromal cells (BMSCs) were considered as one of the strongest candidates for cell transplantations to treat neurological disorders. Previously, we had showed that BMSCs isolated from rats could be induced to differentiate into neural cells being cocultured with olfactory ensheathing cells (OECs). In this study, we further demonstrated the neural differentiation of human BMSCs (hBMSCs) when cocultured with OECs and daily supplement of bFGF (basic fibroblast growth factor). Transwell culture dishes with a 0.4-mm pore size were used to coculture hBMSCs and OECs. At different time points (12h, 24h, 3d, 7d, 14d), the induced hBMSCs were morphologically observed and performed immunocytofluorescence and quantitative RT-PCR (qRT-PCR). The number of neural markers-positive cells significantly increased after coculture, and gene expression of NSE, β-III-tubulin, MAP2, GFAP also dramatically increased. Our study suggested that hBMSCs could be induced into neuron-like cells under conditions of coculture with OECs and daily supplement of bFGF. The differentiated autologous hBMSCs had a great potential for transplantation to treat CNS lesion.
机译:骨髓基质细胞(BMSC)被认为是用于治疗神经系统疾病的细胞移植的最强候选者之一。以前,我们已经表明,从大鼠中分离出的BMSC可以被诱导分化为与嗅鞘细胞(OEC)共培养的神经细胞。在这项研究中,我们进一步证明了与OEC和每日补充bFGF(碱性成纤维细胞生长因子)共培养时,人BMSC(hBMSC)的神经分化。使用孔径为0.4 mm的Transwell培养皿共培养hBMSC和OEC。在不同时间点(12h,24h,3d,7d,14d),观察诱导的hBMSCs的形态,并进行免疫细胞荧光和定量RT-PCR(qRT-PCR)。共培养后,神经标志物阳性细胞的数量显着增加,NSE,β-III-微管蛋白,MAP2,GFAP的基因表达也显着增加。我们的研究表明,在与OECs和bFGF每天补充一起共培养的条件下,hBMSCs可以被诱导为神经元样细胞。分化的自体hBMSCs具有治疗中枢神经系统病变的巨大潜力。

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