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首页> 外文期刊>International Journal of Neural Systems >Quantitative Analysis of Rat Dorsal Root Ganglion Neurons Cultured on Microelectrode Arrays Based on Fluorescence Microscopy Image Processing
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Quantitative Analysis of Rat Dorsal Root Ganglion Neurons Cultured on Microelectrode Arrays Based on Fluorescence Microscopy Image Processing

机译:基于荧光显微镜图像处理的微电极阵列培养的大鼠背根神经节神经元定量分析

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摘要

Microelectrode Arrays (MEA) are devices for long term electrophysiological recording of extracellular spontaneous or evocated activities on in vitro neuron culture. This work proposes and develops a framework for quantitative and morphological analysis of neuron cultures on MEAs, by processing their corresponding images, acquired by fluorescence microscopy. The neurons are segmented from the fluorescence channel images using a combination of segmentation by thresholding, watershed transform, and object classification. The positioning of microelectrodes is obtained from the transmitted light channel images using the circular Hough transform. The proposed method was applied to images of dissociated culture of rat dorsal root ganglion (DRG) neuronal cells. The morphological and topological quantitative analysis carried out produced information regarding the state of culture, such as population count, neuron-to-neuron and neuron-to-microelectrode distances, soma morphologies, neuron sizes, neuron and microelectrode spatial distributions. Most of the analysis of microscopy images taken from neuronal cultures on MEA only consider simple qualitative analysis. Also, the proposed framework aims to standardize the image processing and to compute quantitative useful measures for integrated image-signal studies and further computational simulations. As results show, the implemented microelectrode identification method is robust and so are the implemented neuron segmentation and classification one (with a correct segmentation rate up to 84%). The quantitative information retrieved by the method is highly relevant to assist the integrated signal-image study of recorded electrophysiological signals as well as the physical aspects of the neuron culture on MEA. Although the experiments deal with DRG cell images, cortical and hippocampal cell images could also be processed with small adjustments in the image processing parameter estimation.
机译:微电极阵列(MEA)是用于长期电生理记录体外神经元培养中细胞外自发或激发活动的设备。这项工作提出并开发了一个框架,用于通过处理通过荧光显微镜获得的相应图像,对MEA上的神经元培养物进行定量和形态分析。使用通过阈值分割,分水岭变换和对象分类的组合,从荧光通道图像中分割神经元。使用圆形霍夫变换从透射光通道图像获得微电极的位置。该方法应用于大鼠背根神经节(DRG)神经元细胞解离培养的图像。进行了形态学和拓扑学定量分析,得出了有关文化状况的信息,例如种群数量,神经元到神经元和神经元到微电极的距离,体细胞形态,神经元大小,神经元和微电极的空间分布。在MEA上从神经元文化中获取的显微镜图像的大多数分析仅考虑简单的定性分析。同样,提出的框架旨在标准化图像处理并计算用于集成图像信号研究和进一步计算模拟的定量有用措施。结果表明,所实施的微电极识别方法是鲁棒的,所实施的神经元分割和分类方法也是正确的(正确的分割率高达84%)。通过该方法检索到的定量信息与协助对记录的电生理信号以及MEA上的神经元培养物的物理方面进行综合的信号图像研究非常相关。尽管实验处理的是DRG细胞图像,但也可以在图像处理参数估计中进行较小的调整来处理皮质和海马细胞图像。

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