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用于研究人类神经系统环路的组装体模型。

Assembloid model to study loop circuits of the human nervous system.

作者信息

Miura Yuki, Kim Ji-Il, Jurjuț Ovidiu, Kelley Kevin W, Yang Xiao, Chen Xiaoyu, Thete Mayuri Vijay, Revah Omer, Cui Bianxiao, Pachitariu Marius, Pașca Sergiu P

出版信息

bioRxiv. 2024 Oct 14:2024.10.13.617729. doi: 10.1101/2024.10.13.617729.

Abstract

Neural circuits connecting the cerebral cortex, the basal ganglia and the thalamus are fundamental networks for sensorimotor processing and their dysfunction has been consistently implicated in neuropsychiatric disorders . These recursive, loop circuits have been investigated in animal models and by clinical neuroimaging, however, direct functional access to developing human neurons forming these networks has been limited. Here, we use human pluripotent stem cells to reconstruct an cortico-striatal-thalamic-cortical circuit by creating a four-part loop assembloid. More specifically, we generate regionalized neural organoids that resemble the key elements of the cortico-striatal-thalamic-cortical circuit, and functionally integrate them into loop assembloids using custom 3D-printed biocompatible wells. Volumetric and mesoscale calcium imaging, as well as extracellular recordings from individual parts of these assembloids reveal the emergence of synchronized patterns of neuronal activity. In addition, a multi-step rabies retrograde tracing approach demonstrate the formation of neuronal connectivity across the network in loop assembloids. Lastly, we apply this system to study heterozygous loss of gene associated with autism spectrum disorder and Tourette syndrome and discover aberrant synchronized activity in disease model assembloids. Taken together, this human multi-cellular platform will facilitate functional investigations of the cortico-striatal-thalamic-cortical circuit in the context of early human development and in disease conditions.

摘要

连接大脑皮层、基底神经节和丘脑的神经回路是感觉运动处理的基本网络,其功能障碍一直被认为与神经精神疾病有关。这些递归的环路电路已在动物模型和临床神经影像学中进行了研究,然而,直接功能性地接触形成这些网络的发育中的人类神经元一直受到限制。在这里,我们使用人类多能干细胞通过创建一个四部分的环路组装体来重建皮质-纹状体-丘脑-皮质回路。更具体地说,我们生成了类似于皮质-纹状体-丘脑-皮质回路关键元件的区域化神经类器官,并使用定制的3D打印生物相容性孔将它们功能整合到环路组装体中。体积和中尺度钙成像以及这些组装体各个部分的细胞外记录揭示了神经元活动同步模式的出现。此外,一种多步骤狂犬病逆行追踪方法证明了环路组装体中跨网络的神经元连接的形成。最后,我们应用这个系统来研究与自闭症谱系障碍和妥瑞氏综合征相关的基因的杂合缺失,并在疾病模型组装体中发现异常的同步活动。综上所述,这个人类多细胞平台将有助于在早期人类发育和疾病条件下对皮质-纹状体-丘脑-皮质回路进行功能研究。

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