Neuroscience Axis, Research Center of CHU de Québec-Université Laval, Quebec City, QC, Canada.
Department of Psychiatry and Neuroscience, Faculty of Medicine, Université Laval, Quebec City, QC, Canada.
Sci Rep. 2024 Aug 16;14(1):19035. doi: 10.1038/s41598-024-69426-z.
Glial scar formation represents a fundamental response to central nervous system (CNS) injuries. It is mainly characterized by a well-defined spatial rearrangement of reactive astrocytes and microglia. The mechanisms underlying glial scar formation have been extensively studied, yet quantitative descriptors of the spatial arrangement of reactive glial cells remain limited. Here, we present a novel approach using point pattern analysis (PPA) and topological data analysis (TDA) to quantify spatial patterns of reactive glial cells after experimental ischemic stroke in mice. We provide open and reproducible tools using R and Julia to quantify spatial intensity, cell covariance and conditional distribution, cell-to-cell interactions, and short/long-scale arrangement, which collectively disentangle the arrangement patterns of the glial scar. This approach unravels a substantial divergence in the distribution of GFAP and IBA1 cells after injury that conventional analysis methods cannot fully characterize. PPA and TDA are valuable tools for studying the complex spatial arrangement of reactive glia and other nervous cells following CNS injuries and have potential applications for evaluating glial-targeted restorative therapies.
胶质瘢痕形成代表了中枢神经系统(CNS)损伤的基本反应。它的主要特征是反应性星形胶质细胞和小胶质细胞的明确空间重排。胶质瘢痕形成的机制已经得到了广泛的研究,但反应性胶质细胞空间排列的定量描述仍然有限。在这里,我们使用点模式分析(PPA)和拓扑数据分析(TDA)来定量分析小鼠实验性缺血性中风后反应性胶质细胞的空间模式。我们使用 R 和 Julia 提供了开放和可重复的工具来量化空间强度、细胞协方差和条件分布、细胞间相互作用以及短/长尺度排列,这些共同揭示了胶质瘢痕的排列模式。这种方法揭示了损伤后 GFAP 和 IBA1 细胞分布的实质性差异,这是传统分析方法无法完全描述的。PPA 和 TDA 是研究 CNS 损伤后反应性胶质细胞和其他神经细胞复杂空间排列的有价值的工具,并且有可能用于评估针对胶质细胞的修复治疗。