Impairment of long-term potentiation (LTP) is a common feature of many preclinical models of neurological disorders. Modeling LTP on human induced pluripotent stem cells (hiPSC) enables the investigation of this critical plasticity process in disease-specific genetic backgrounds. Here, we describe a method to chemically induce LTP across entire networks of hiPSC-derived neurons on multi-electrode arrays (MEAs) and investigate effects on neuronal network activity and associated molecular changes.
Keywords: Human-induced pluripotent stem cell-derived neurons; Long-term potentiation; Multi-electrode array; Synaptic plasticity.
© 2023. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.