02107nas a2200313 4500000000100000000000100001008004100002260001100043653000800054653002200062653001300084653002600097653002500123653002200148100002000170700002500190700001600215700002600231700003700257700002000294700001800314700002000332245014500352856004500497300000900542490000700551520122100558022001401779 2023 d c2023/110aIPS10aElectrophysiology10aepilepsy10amicroelectrode arrays10aneurological disease10aneuronal networks1 aMichel H. Y. Hu1 aJean-Philippe Frimat1 aKim Rijkers1 aOlaf E. M. G. Schijns1 aArn M. J. M. van den Maagdenberg1 aJim T. A. Dings1 aRegina Luttge1 aGovert Hoogland00aSpontaneous Epileptic Recordings from hiPSC-Derived Cortical Neurons Cultured with a Human Epileptic Brain Biopsy on a Multi Electrode Array uhttps://www.mdpi.com/2076-3417/13/3/1432 a14320 v133 aA growing societal awareness is calling upon scientists to reconsider the use of animals in research, which stimulates the development of translational in vitro models. The physiological and architectural interactions between different cell types within an organ present a challenge to these models, particularly for a complex organ such as the brain. Thus far, in vitro brain models mostly consist of a single cell type and demonstrate little predictive value. Here, we present a co-culture of an epileptic human neocortical biopsy on a layer of human induced pluripotent stem cell (hiPSC)-derived cortical neurons. The activity of the cortical neurons was recorded by a 120-electrode multi-electrode array. Recordings were obtained at 0, 3, and 6 days after assembly and compared to those obtained from cortical neurons without a biopsy. On all three recording days, the hybrid model displayed a firing rate, burst behavior, number of isolated spikes, inter-spike interval, and network bursting pattern that aligns with the characteristics of an epileptic network as reported by others. Thus, this novel model may be a non-animal, translational alternative for testing new therapies up to six days after resection. a2076-3417