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Physiological maturation and drug responses of human induced pluripotent stem cell-derived cortical neuronal networks in long-term culture

机译:长期培养的人诱导多能干细胞来源的皮质神经元网络的生理成熟和药物反应

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摘要

The functional network of human induced pluripotent stem cell (hiPSC)-derived neurons is a potentially powerful in vitro model for evaluating disease mechanisms and drug responses. However, the culture time required for the full functional maturation of individual neurons and networks is uncertain. We investigated the development of spontaneous electrophysiological activity and pharmacological responses for over 1 year in culture using multi-electrode arrays (MEAs). The complete maturation of spontaneous firing, evoked responses, and modulation of activity by glutamatergic and GABAergic receptor antagonists/agonists required 20–30 weeks. At this stage, neural networks also demonstrated epileptiform synchronized burst firing (SBF) in response to pro-convulsants and SBF suppression using clinical anti-epilepsy drugs. Our results reveal the feasibility of long-term MEA measurements from hiPSC-derived neuronal networks in vitro for mechanistic analyses and drug screening. However, developmental changes in electrophysiological and pharmacological properties indicate the necessity for the international standardization of culture and evaluation procedures.
机译:人类诱导的多能干细胞(hiPSC)衍生的神经元的功能网络是用于评估疾病机制和药物反应的潜在强大的体外模型。但是,单个神经元和网络完全功能成熟所需的培养时间尚不确定。我们调查了使用多电极阵列(MEA)在培养中自发1年以上的自发电生理活性和药理反应的发展。谷氨酸能和GABA能受体拮抗剂/激动剂能够完全成熟自发放电,诱发反应并调节活性,需要20-30周。在此阶段,神经网络还证明了使用临床抗癫痫药对前惊厥药和SBF的抑制作用可产生癫痫样同步放电(SBF)。我们的结果揭示了从hiPSC衍生的神经元网络进行长期MEA测量以进行机械分析和药物筛选的可行性。但是,电生理学和药理学性质的发展变化表明文化和评估程序国际标准化的必要性。

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