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首页> 外文期刊>Stem cell research >Three dimensional cellular microarray platform for human neural stem cell differentiation and toxicology - ScienceDirect
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Three dimensional cellular microarray platform for human neural stem cell differentiation and toxicology - ScienceDirect

机译:用于人类神经干细胞分化和毒理学的三维细胞微阵列平台-ScienceDirect

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We developed a three-dimensional (3D) cellular microarray platform for the high-throughput (HT) analysis of human neural stem cell (hNSC) growth and differentiation. The growth of an immortalized hNSC line, ReNcell VM, was evaluated on a miniaturized cell culture chip consisting of 60?nl spots of cells encapsulated in alginate, and compared to standard 2D well plate culture conditions. Using a live/dead cell viability assay, we demonstrated that the hNSCs are able to expand on-chip, albeit with lower proliferation rates and viabilities than in conventional 2D culture platforms. Using an in-cell, on-chip immunofluorescence assay, which provides quantitative information on cellular levels of proteins involved in neural fate, we demonstrated that ReNcell VM can preserve its multipotent state during on-chip expansion. Moreover, differentiation of the hNSCs into glial progeny was achieved both off- and on-chip six days after growth factor removal, accompanied by a decrease in the neural progenitor markers. The versatility of the platform was further demonstrated by complementing the cell culture chip with a chamber system that allowed us to screen for differential toxicity of small molecules to hNSCs. Using this approach, we showed differential toxicity when evaluating three neurotoxic compounds and one antiproliferative compound, and the null effect of a non-toxic compound at relevant concentrations. Thus, our 3D high-throughput microarray platform may help predict, in vitro, which compounds pose an increased threat to neural development and should therefore be prioritized for further screening and evaluation.
机译:我们开发了用于人类神经干细胞(hNSC)生长和分化的高通量(HT)分析的三维(3D)细胞微阵列平台。在微型细胞培养芯片上评估了永生化hNSC系ReNcell VM的生长,该芯片由60µl藻酸盐包封的细胞斑点组成,并与标准2D孔板培养条件进行了比较。使用活/死细胞活力测定法,我们证明了hNSCs能够在芯片上扩展,尽管其增殖率和活力均低于常规2D培养平台。使用细胞内片上免疫荧光测定法可提供有关神经命运相关蛋白质的细胞水平的定量信息,我们证明ReNcell VM可以在片上扩展过程中保持其多能状态。此外,hNSCs分化为神经胶质后代的实现是在生长因子去除后六天的芯片内和芯片外实现的,同时神经祖细胞标记物减少。该平台的多功能性通过用室系统补充细胞培养芯片而得到进一步证明,该室系统使我们能够筛选小分子对hNSC的不同毒性。使用这种方法,我们在评估三种神经毒性化合物和一种抗增殖化合物时表现出不同的毒性,而在相关浓度下无毒化合物的无效作用。因此,我们的3D高通量微阵列平台可以在体外帮助预测哪些化合物对神经发育的威胁增加,因此应优先考虑进一步筛选和评估。

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