Jones Hannah E, Abrams Kelsey A, Siegenthaler Julie A
University of Colorado Anschutz Medical Campus, Department of Pediatrics, Section of Developmental Biology, Aurora, Colorado, United States.
University of Colorado Anschutz Medical Campus; Cell Biology, Stem Cells, and Development Graduate Program; Aurora, Colorado, United States.
Neurophotonics. 2022 Apr;9(2):021911. doi: 10.1117/1.NPh.9.2.021911. Epub 2022 Apr 5.
Fibroblasts are found associated with blood vessels in various locations across the central nervous system (CNS): in the meninges, the choroid plexus, and in the parenchyma within perivascular spaces. CNS fibroblasts have been characterized using transcriptional profiling and a mouse line used to identify CNS fibroblasts ; however, we still know very little regarding their functions and identity. Current methods for visualizing CNS fibroblasts are lacking and, in particular, prevent adequate assessment of fibroblast-vessel interactions. We aimed to develop new ways to visualize CNS fibroblasts in greater detail. : Here, we describe methods for whole mount visualization of meningeal and choroid plexus fibroblasts, and CUBIC optical tissue clearing methods for visualization of parenchymal vessel-associated fibroblasts. We show that these methods can be used for visualization of vessel-fibroblast interactions in these CNS structures and provide significant improvement over traditional sectioning and staining methods. In addition, we can combine these techniques with immunohistochemistry methods for labeling different cell types in the meninges and blood vasculature as well as EdU-based cell proliferation assays. We expect these methods will advance studies of CNS fibroblast development and functions in homeostasis, injury, and disease.
在中枢神经系统(CNS)的各个位置都发现成纤维细胞与血管相关:在脑膜、脉络丛以及血管周围间隙内的实质组织中。已经利用转录谱分析和一种用于识别中枢神经系统成纤维细胞的小鼠品系对中枢神经系统成纤维细胞进行了表征;然而,我们对它们的功能和特性仍然知之甚少。目前缺乏可视化中枢神经系统成纤维细胞的方法,尤其是无法充分评估成纤维细胞与血管的相互作用。我们旨在开发更详细地可视化中枢神经系统成纤维细胞的新方法。在此,我们描述了脑膜和脉络丛成纤维细胞的整体装片可视化方法,以及用于可视化实质血管相关成纤维细胞的CUBIC光学组织透明化方法。我们表明,这些方法可用于可视化这些中枢神经系统结构中的血管 - 成纤维细胞相互作用,并且比传统的切片和染色方法有显著改进。此外,我们可以将这些技术与免疫组织化学方法相结合,用于标记脑膜和血管系统中的不同细胞类型以及基于EdU的细胞增殖测定。我们期望这些方法将推动对中枢神经系统成纤维细胞在稳态、损伤和疾病中的发育和功能的研究。