The discovery of therapeutics for neurological diseases is hindered by the lack of predictive in vitro and in vivo models. Traditional in vitro assays rely on 2D-engineered cell lines, which are suitable for large-scale screening but lack physiological relevance. Human induced pluripotent stem cell (iPSC)-derived 3D neural spheroids offer a more physiologically relevant alternative, incorporating complex neuronal and glial cell populations that exhibit synchronous activity. This study evaluates the potential of iPSC-derived cortical neural spheroids as a high-throughput screening (HTS) platform for drug discovery by assessing a library of 687 neuroactive compounds. Calcium activity, measured as a functional biomarker, was analyzed using multiparametric data analysis, demonstrating the robustness and applicability of this approach for pharmacological screening.
This study demonstrates that iPSC-derived cortical neural spheroids serve as a robust, physiologically relevant platform for high-throughput pharmacological screening. The integration of multiparametric calcium fluorescence analysis allows for detailed classification of neuroactive compound responses, offering a powerful tool for advancing neurological disease research and drug discovery efforts.
Boutin, M. E., Strong, C. E., Van Hese, B., Hu, X., Itkin, Z., Chen, Y.-C., LaCroix, A., Gordon, R., Guicherit, O., Carromeu, C., Kundu, S., Lee, E., & Ferrer, M. (2022). A multiparametric calcium signal screening platform using iPSC-derived cortical neural spheroids. SLAS Discovery, 27(3), 209–218.