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Quantitative profiling of microglia populations using harmonic co-clustering of arbor morphology measurements

机译:使用乔木形态测量的谐波共聚对小胶质细胞种群进行定量分析

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Microglia are the resident immune cell population in the mammalian central nervous system (CNS). These highly plastic cells exhibit ramified arbors in their resting state, and progressively less-complex arbors when activated. Our goal is to compare the spatial distributions of resting and activated microglia in normal brain tissue against tissue that is perturbed by insertion of a neural recording device. For this, microglia were imaged using multiplex immunostaining and confocal microscopy. The cell arbors were traced automatically, and 127 quantitative measurements based on the L-measure [8] were computed for each cell. A hierarchical extension of Coifman's [1,2] unsupervised harmonic analysis method was used to profile these multivariate data and identify groups of similar cells and the underlying features. This iterative procedure induces an orthogonal basis by constructing a coupled geometry over the row and column spaces of the feature matrix. Smoothing of the dataset, and the row and column clusters is achieved simultaneously when the algorithm converges. Experiments on real image datasets demonstrate the ability of this method to generate qualitative and quantitative groups that are biologically meaningful despite the existence of noise and missing values.
机译:小胶质细胞是哺乳动物中枢神经系统(CNS)中的常驻免疫细胞群。这些高度可塑性的细胞在其静止状态下显示出分支的乔木,并在激活时逐渐变得不那么复杂。我们的目标是比较正常脑组织中静息和激活的小胶质细胞的空间分布与插入神经记录设备所扰动的组织的空间分布。为此,使用多重免疫染色和共聚焦显微镜对小胶质细胞成像。自动跟踪细胞的乔木,并为每个细胞计算了基于L量度[8]的127个定量测量值。使用Coifman [1,2]无监督谐波分析方法的层次扩展来剖析这些多元数据,并识别相似单元的组和潜在特征。通过在特征矩阵的行和列空间上构造耦合的几何图形,此迭代过程可得出正交基础。当算法收敛时,可以同时实现数据集的平滑以及行和列的聚类。在真实图像数据集上进行的实验表明,该方法能够生成定性和定量的组,尽管存在噪声和缺失值,但它们在生物学上还是有意义的。

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