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成年鼠背根神经节神经元在分离培养中形成异常的谷氨酸能连接。

Adult mouse dorsal root ganglia neurons form aberrant glutamatergic connections in dissociated cultures.

机构信息

Institute of Biomedical Engineering, Bogazici University, İstanbul, Turkey.

Department of Electrical and Electronics Engineering, Faculty of Engineering, Marmara University, İstanbul, Turkey.

出版信息

PLoS One. 2021 Mar 3;16(3):e0246924. doi: 10.1371/journal.pone.0246924. eCollection 2021.

Abstract

Cultured sensory neurons can exhibit complex activity patterns following stimulation in terms of increased excitability and interconnected responses of multiple neurons. Although these complex activity patterns suggest a network-like configuration, research so far had little interest in synaptic network formation ability of the sensory neurons. To identify interaction profiles of Dorsal Root Ganglia (DRG) neurons and explore their putative connectivity, we developed an in vitro experimental approach. A double transgenic mouse model, expressing genetically encoded calcium indicator (GECI) in their glutamatergic neurons, was produced. Dissociated DRG cultures from adult mice were prepared with a serum-free protocol and no additional growth factors or cytokines were utilized for neuronal sensitization. DRG neurons were grown on microelectrode arrays (MEA) to induce stimulus-evoked activity with a modality-free stimulation strategy. With an almost single-cell level electrical stimulation, spontaneous and evoked activity of GCaMP6s expressing neurons were detected under confocal microscope. Typical responses were analyzed, and correlated calcium events were detected across individual DRG neurons. Next, correlated responses were successfully blocked by glutamatergic receptor antagonists, which indicated functional synaptic coupling. Immunostaining confirmed the presence of synapses mainly in the axonal terminals, axon-soma junctions and axon-axon intersection sites. Concisely, the results presented here illustrate a new type of neuron-to-neuron interaction in cultured DRG neurons conducted through synapses. The developed assay can be a valuable tool to analyze individual and collective responses of the cultured sensory neurons.

摘要

培养的感觉神经元在受到刺激后会表现出复杂的活动模式,表现为兴奋性增加和多个神经元的相互关联反应。尽管这些复杂的活动模式表明存在网络状结构,但迄今为止,研究对感觉神经元的突触网络形成能力几乎没有兴趣。为了确定背根神经节 (DRG) 神经元的相互作用谱并探索其潜在的连接性,我们开发了一种体外实验方法。制作了一种双转基因小鼠模型,在其谷氨酸能神经元中表达基因编码的钙指示剂 (GECI)。使用无血清方案从成年小鼠中分离 DRG 培养物,并在神经元敏化过程中不使用任何额外的生长因子或细胞因子。将 DRG 神经元种植在微电极阵列 (MEA) 上,使用无模态刺激策略诱导刺激诱发的活动。通过几乎单细胞水平的电刺激,在共聚焦显微镜下检测到表达 GCaMP6s 的神经元的自发和诱发活动。分析了典型的反应,并在单个 DRG 神经元之间检测到相关的钙事件。接下来,用谷氨酸能受体拮抗剂成功阻断了相关反应,这表明存在功能突触耦联。免疫染色证实了突触主要存在于轴突末梢、轴突-体节连接处和轴突-轴突交叉点。简而言之,这里呈现的结果说明了在培养的 DRG 神经元中通过突触进行的一种新型神经元间相互作用。开发的测定法可以成为分析培养感觉神经元的个体和集体反应的有价值的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/797b/7928449/47118b45a07b/pone.0246924.g001.jpg

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