Courtney Jo-Maree, Morris Gary P, Cleary Elise M, Howells David W, Sutherland Brad A
Tasmanian School of Medicine, College of Health and Medicine, University of Tasmania, Hobart, Tasmania, Australia.
Bio Protoc. 2022 Jul 5;12(13). doi: 10.21769/BioProtoc.4459.
The quantification of labeled cells in tissue sections is crucial to the advancement of biological knowledge. Traditionally, this was a tedious process, requiring hours of careful manual counting in small portions of a larger tissue section. To overcome this, many automated methods for cell analysis have been developed. Recent advances in whole slide scanning technologies have provided the means to image cells in entire tissue sections. However, common automated analysis tools do not have the capacity to deal with the large image files produced. Herein, we present a protocol for the quantification of two fluorescently labeled cell populations, namely pericytes and microglia, in whole brain tissue sections. This protocol uses custom-made scripts within the open source software QuPath to provide a framework for the careful optimization and validation of automated cell detection parameters. Images obtained from a whole-slide scanner are first loaded into a QuPath project. Manual counts are performed on small sample regions to optimize cell detection parameters prior to automated quantification of cells across entire brain regions. Even though we have quantified pericytes and microglia, any fluorescently labeled cell with clear labeling in and around the nucleus can be analyzed using these methods. This protocol provides a user-friendly and cost-effective framework for the automated analysis of whole tissue sections.
组织切片中标记细胞的定量对于生物学知识的进步至关重要。传统上,这是一个繁琐的过程,需要在较大组织切片的小部分中进行数小时的仔细手动计数。为了克服这一问题,已经开发了许多细胞分析的自动化方法。全玻片扫描技术的最新进展提供了对整个组织切片中的细胞进行成像的手段。然而,常见的自动化分析工具没有能力处理所产生的大型图像文件。在此,我们提出了一种在全脑组织切片中对两种荧光标记细胞群体(即周细胞和小胶质细胞)进行定量的方案。该方案使用开源软件QuPath中的定制脚本,为仔细优化和验证自动化细胞检测参数提供一个框架。从全玻片扫描仪获得的图像首先加载到QuPath项目中。在对整个脑区的细胞进行自动定量之前,先在小样本区域进行手动计数以优化细胞检测参数。尽管我们已经对周细胞和小胶质细胞进行了定量,但任何在细胞核内和周围有清晰标记的荧光标记细胞都可以使用这些方法进行分析。该方案为全组织切片的自动化分析提供了一个用户友好且经济高效的框架。