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首页> 外文期刊>Archives of medical research >Umbilical Cord Blood Cells CD133+/CD133- Cultivation in Neural Proliferation Media Differentiates Towards Neural Cell Lineages
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Umbilical Cord Blood Cells CD133+/CD133- Cultivation in Neural Proliferation Media Differentiates Towards Neural Cell Lineages

机译:在神经增殖培养基中培养的脐带血细胞CD133 + / CD133-分化为神经细胞谱系

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Background and Aims. Umbilical cord blood (UCB) has been identified as a good source of hematopoietic and nonhematopoietic stem cells that can be easily isolated. In the present study we investigated the possibility of whether stem cells in mononuclear UCB grown under defined conditions can produce progeny with neural phenotype.Methods. A combination of antigen-driven magnetic cell sorting (MACs) method and defined culture conditions specific for cells of neural lineages were used for isolation, expansion and differentiation of CD133+/- cells from UCB. Both UCB-derived fractions were expanded by exposure to growth factors (EGF, bFGF). Differentiation was induced by replacing them with fetal bovine serum. Using immunocytochemistry, the cell markers for neural (MAP2, GFAP, RIP) and non-neural lineages (S-100, von Willebrand factor) were detected.Results. The analysis revealed occurrence of fully mature neural and non-neural lineages, which showed qualitative and quantitative differences between population of CD 133+ and CD 133- cells. The expression levels of MAP2 and RIP in CD 133+ were significantly higher than in CD 133-, more GFAP positive cells were found in the CD 133-. At the same time, S-100 was expressed by 32.47 ± 6.24% of CD 133- cells and 29.42 ± 1.32% of CD 133- cell expressed a von Willebrand factor antigen.Conclusions. Our results indicate that stem cells derived from umbilical cord blood are easy to obtain, proliferate and are able to differentiate towards the cells of neural lineages, which represents a promising way for their utilization in cell-based therapies for CNS injuries and diseases.
机译:背景和目标。脐带血(UCB)已被确定为造血干细胞和非造血干细胞的良好来源,可以很容易地对其进行分离。在本研究中,我们调查了在特定条件下生长的单核UCB中的干细胞是否可以产生具有神经表型的后代的可能性。将抗原驱动的磁性细胞分选(MACs)方法和特定于神经谱系细胞的特定培养条件结合起来,用于从UCB中分离,扩增和分化CD133 +/-细胞。通过暴露于生长因子(EGF,bFGF),两种UCB衍生的级分均得以扩增。通过用胎牛血清代替它们来诱导分化。使用免疫细胞化学技术检测了神经(MAP2,GFAP,RIP)和非神经谱系(S-100,von Willebrand因子)的细胞标志物。该分析揭示了完全成熟的神经和非神经谱系的发生,这表明了CD 133+和CD 133-细胞群体之间的定性和定量差异。 CD 133+中MAP2和RIP的表达水平显着高于CD 133-中,在CD 133-中发现了更多的GFAP阳性细胞。同时,S-100在32.47±6.24%的CD 133-细胞中表达,29.42±1.32%的CD 133-细胞表达von Willebrand因子抗原。我们的结果表明,源自脐带血的干细胞易于获得,增殖并能够向神经谱系细胞分化,这代表了它们在基于细胞的中枢神经系统损伤和疾病治疗中的应用前景广阔。

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