TY - JOUR
T1 - Three dimensional cellular microarray platform for human neural stem cell differentiation and toxicology
AU - Meli, Luciana
AU - Barbosa, Hélder S.C.
AU - Hickey, Anne Marie
AU - Gasimli, Leyla
AU - Nierode, Gregory
AU - Diogo, Maria Margarida
AU - Linhardt, Robert J.
AU - Cabral, Joaquim M.S.
AU - Dordick, Jonathan S.
N1 - Funding Information:
The authors would like to thank Dr. Sandrine Lavenus and Dr. Seok Joon Kwon for important discussions. This research was supported by the National Institutes of Health ( ES-020903 ). HSCB acknowledges support from the PhD program on Bioengineering: Cell Therapies and Regenerative Medicine (PD/00015/2012) funded by the Portuguese Government (Fundação para a Ciência e a Tecnologia) .
PY - 2014/7
Y1 - 2014/7
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=84899847797&partnerID=8YFLogxK
U2 - 10.1016/j.scr.2014.04.004
DO - 10.1016/j.scr.2014.04.004
M3 - Article
C2 - 24816401
AN - SCOPUS:84899847797
SN - 1873-5061
VL - 13
SP - 36
EP - 47
JO - Stem Cell Research
JF - Stem Cell Research
IS - 1
ER -