Meli Luciana, Barbosa Hélder S C, Hickey Anne Marie, Gasimli Leyla, Nierode Gregory, Diogo Maria Margarida, Linhardt Robert J, Cabral Joaquim M S, Dordick Jonathan S
Department of Chemical and Biological Engineering, Rensselaer Polytechnic Institute, 110 8th Street, Troy, NY, USA.
Institute for Biotechnology and Bioengineering, Instituto Superior Técnico, University of Lisbon, Portugal; Department of Bioengineering, Instituto Superior Técnico, University of Lisbon, Portugal.
Stem Cell Res. 2014 Jul;13(1):36-47. doi: 10.1016/j.scr.2014.04.004. Epub 2014 Apr 18.
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 60nl 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.
我们开发了一种三维(3D)细胞微阵列平台,用于对人类神经干细胞(hNSC)的生长和分化进行高通量(HT)分析。在一个由封装于藻酸盐中的60nl细胞点组成的小型化细胞培养芯片上评估了永生化hNSC系ReNcell VM的生长情况,并与标准的二维孔板培养条件进行了比较。通过活/死细胞活力测定,我们证明hNSCs能够在芯片上扩增,尽管其增殖率和活力低于传统的二维培养平台。利用细胞内芯片免疫荧光测定法,该方法可提供有关神经命运相关蛋白质细胞水平的定量信息,我们证明ReNcell VM在芯片上扩增过程中能够保持其多能状态。此外,在去除生长因子六天后,hNSCs在芯片外和芯片上均分化为神经胶质后代,同时神经祖细胞标志物减少。通过用一个腔室系统对细胞培养芯片进行补充,进一步证明了该平台的多功能性,该腔室系统使我们能够筛选小分子对hNSCs的差异毒性。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显示出差异毒性,以及一种无毒化合物在相关浓度下的无效作用。因此,我们的3D高通量微阵列平台可能有助于在体外预测哪些化合物对神经发育构成更大威胁,因此应优先进行进一步的筛选和评估。