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高通量分析电刺激神经元培养物中的突触活动。

High-throughput Analysis of Synaptic Activity in Electrically Stimulated Neuronal Cultures.

机构信息

Laboratory of Cell Biology and Histology, University of Antwerp, CDE, Antwerp, Belgium.

Janssen Research and Development, Neuroscience Therapeutic Area, Beerse, Belgium.

出版信息

Neuroinformatics. 2021 Oct;19(4):737-750. doi: 10.1007/s12021-021-09536-5. Epub 2021 Aug 10.

Abstract

Synaptic dysfunction is a hallmark of various neurodegenerative and neurodevelopmental disorders. To interrogate synapse function in a systematic manner, we have established an automated high-throughput imaging pipeline based on fluorescence microscopy acquisition and image analysis of electrically stimulated synaptic transmission in neuronal cultures. Identification and measurement of synaptic signal fluctuations is achieved by means of an image analysis algorithm based on singular value decomposition. By exploiting the synchronicity of the evoked responses, the algorithm allows disentangling distinct temporally correlated patterns of firing synapse populations or cell types that are present in the same recording. We demonstrate the performance of the analysis with a pilot compound screen and show that the multiparametric readout allows classifying treatments by their spatiotemporal fingerprint. The image analysis and visualization software has been made publicly available on Github ( https://www.github.com/S3Toolbox ). The streamlined automation of multi-well image acquisition, electrical stimulation, analysis, and meta-data warehousing facilitates large-scale synapse-oriented screens and, in doing so, it will accelerate the drug discovery process.

摘要

突触功能障碍是各种神经退行性和神经发育性疾病的标志。为了系统地研究突触功能,我们建立了一个基于荧光显微镜采集和神经元培养中电刺激突触传递的图像分析的自动化高通量成像管道。通过基于奇异值分解的图像分析算法,可以实现突触信号波动的识别和测量。通过利用诱发反应的同步性,该算法允许在同一记录中分离出存在于同一记录中的不同时间相关的发射突触群体或细胞类型的模式。我们用一个先导化合物筛选来证明分析的性能,并表明多参数读数可以根据其时空指纹对处理进行分类。图像分析和可视化软件已在 Github 上(https://www.github.com/S3Toolbox)公开。多井图像采集、电刺激、分析和元数据仓库的流线型自动化促进了大规模面向突触的筛选,从而加速了药物发现过程。

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