Abstract

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.

Highlights

  • Neurotoxicity detection is a major challenge due to the complexity of the central and peripheral nervous systems

  • The majority of commercial chemicals have not been evaluated for developmental neurotoxicity, at least partly due to the high cost of animal testing (National Research Council 2007)

  • Regulatory agencies have traditionally used in vivo methods for adult and developmental neurotoxicity testing, including neurobehavioral evaluation of cognitive, sensory and motor functions accompanied by neuropathological studies, with no specific studies of the underlying cell biology (Bal-Price et al 2010)

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Summary

Introduction

Neurotoxicity detection is a major challenge due to the complexity of the central and peripheral nervous systems. There is a need to test large sets of compounds to comply with specific regulatory requirements (Breier et al 2010; Andersen & Krewski 2009) To this end, there is pressure to develop alternative test strategies, which are rapid, economical, and, most critically, highly predictive (Breier et al 2010). The development of new high-throughput screening tools that enable the study of these differential effects on stem cells and their differentiated progeny, should encompass endpoints that assess chemical toxicity, and allow us to determine stem cell fate. This is generally achieved by following protein markers of multipotency and differentiation

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