Human Neural Organoid Microphysiological Systems Show the Building Blocks Necessary for Basic Learning and Memory

Dowlette-Mary Alam El Din, Leah Moenkemoeller, Alon Loeffler, Forough Habibollahi, Jack Schenkman, Amitav Mitra, Tjitse van der Molen, Lixuan Ding, Jason Laird, Maren Schenke, Erik Johnson, Brett Kagan, Thomas Hartung, Lena Smirnova
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Abstract

Brain Microphysiological Systems including neural organoids derived from human induced pluripotent stem cells offer a unique lens to study the intricate workings of the human brain. This paper investigates the foundational elements of learning and memory in neural organoids, also known as Organoid Intelligence by quantifying immediate early gene expression, synaptic plasticity, neuronal network dynamics, and criticality to demonstrate the utility of these organoids in basic science research. Neural organoids showed synapse formation, glutamatergic and GABAergic receptor expression, immediate early gene expression basally and evoked, functional connectivity, criticality, and synaptic plasticity in response to theta-burst stimulation. In addition, pharmacological interventions on GABAergic and glutamatergic receptors, and input specific theta-burst stimulation further shed light on the capacity of neural organoids to mirror synaptic modulation and short-term potentiation, demonstrating their potential as tools for studying neurophysiological and neurological processes and informing therapeutic strategies for diseases.
人类神经有机体微观生理系统展示了基本学习和记忆所需的基石
脑微生理系统(包括从人类诱导多能干细胞中提取的神经有机体)为研究人类大脑的复杂运作提供了一个独特的视角。本文通过量化即时早期基因表达、突触可塑性、神经元网络动态和临界性,研究了神经器官(又称器官智能)中学习和记忆的基本要素,以证明这些器官在基础科学研究中的实用性。神经器官模型显示了突触的形成、谷氨酸能和 GABA 能受体的表达、基础和诱发的即刻早期基因表达、功能连接性、临界性,以及θ-脉冲刺激下的突触可塑性。此外,对GABA能受体和谷氨酸能受体的药物干预,以及输入特定的θ-脉冲刺激,进一步揭示了神经器官组织反映突触调节和短期延时的能力,显示了它们作为研究神经生理和神经过程的工具以及为疾病治疗策略提供信息的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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