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Synchronous firing patterns of induced pluripotent stem cell-derived cortical neurons depend on the network structure consisting of excitatory and inhibitory neurons

机译:诱导多能干细胞衍生皮质神经元的同步烧制模式取决于由兴奋性和抑制神经元组成的网络结构

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The balance between glutamate-mediated excitation and GABA-mediated inhibition is critical to cortical functioning. However, the contribution of network structure consisting of the both neurons to cortical functioning has not been elucidated. We aimed to evaluate the relationship between the network structure and functional activity patterns in vitro. We used mouse induced pluripotent stem cells (iPSCs) to construct three types of neuronal populations; excitatory-rich (Exc), inhibitory-rich (Inh), and control (Cont). Then, we analyzed the activity patterns of these neuronal populations using microelectrode arrays (MEAs). Inhibitory synaptic densities differed between the three types of iPSC-derived neuronal populations, and the neurons showed spontaneously synchronized bursting activity with functional maturation for one month. Moreover, different firing patterns were observed between the three populations; Exc demonstrated the highest firing rates, including frequent, long, and dominant bursts. In contrast, lnh demonstrated the lowest firing rates and the least dominant bursts. Synchronized bursts were enhanced by disinhibition via GABA(A) receptor blockade. The present study, using iPSC-derived neurons and MEAs, for the first time show that synchronized bursting of cortical networks in vitro depends on the network structure consisting of excitatory and inhibitory neurons. (C) 2018 Elsevier Inc. All rights reserved.
机译:谷氨酸介导的激发和GABA介导的抑制之间的平衡对于皮质功能至关重要。然而,没有阐明由神经元以皮质功能组成的网络结构的贡献。我们旨在评估网络结构与体外功能模式之间的关系。我们使用小鼠诱导的多能干细胞(IPSC)构建三种类型的神经元群体;富有兴奋性(Exc),抑制性(INH)和控制(续)。然后,我们使用微电极阵列(MEA)分析了这些神经元群的活动模式。抑制性突触密度不同于三种IPSC衍生的神经元群体之间,并且神经元显示出自发同步的爆破活性,具有一个月的功能成熟。此外,在三个群体之间观察到不同的烧制模式; Exc展示了最高的射击率,包括频繁,长,优势突发。相比之下,LNH展示了最低的射击率和最常见的突发。通过GABA(A)受体封锁的呼吁增强了同步突发。本研究首次表明,使用IPSC衍生的神经元和MEAS显示,在体外同步皮质网络的突破取决于由兴奋性和抑制性神经元组成的网络结构。 (c)2018年Elsevier Inc.保留所有权利。

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