Jaros Josef, Petrov Michal, Tesarova Marketa, Hampl Ales
Faculty of Medicine, Department of Histology and Embryology, Masaryk University, Kamenice 3/A1, 625 00, Brno, Czech Republic.
Cell and Tissue Regeneration, International Clinical Research Center, St. Anne's University Hospital Brno, Pekarska 53, 656 91, Brno, Czech Republic.
Methods Mol Biol. 2017;1612:417-431. doi: 10.1007/978-1-4939-7021-6_30.
Cell culture methods have been developed in efforts to produce biologically relevant systems for developmental and disease modeling, and appropriate analytical tools are essential. Knowledge of ultrastructural characteristics represents the basis to reveal in situ the cellular morphology, cell-cell interactions, organelle distribution, niches in which cells reside, and many more. The traditional method for 3D visualization of ultrastructural components, serial sectioning using transmission electron microscopy (TEM), is very labor-intensive due to contentious TEM slice preparation and subsequent image processing of the whole collection. In this chapter, we present serial block-face scanning electron microscopy, together with complex methodology for spheroid formation, contrasting of cellular compartments, image processing, and 3D visualization. The described technique is effective for detailed morphological analysis of stem cell spheroids, organoids, as well as organotypic cell cultures.
为了开发用于发育和疾病建模的具有生物学相关性的系统,人们已经开发了细胞培养方法,并且合适的分析工具至关重要。超微结构特征的知识是原位揭示细胞形态、细胞间相互作用、细胞器分布、细胞所处微环境等的基础。用于超微结构成分三维可视化的传统方法,即使用透射电子显微镜(TEM)进行连续切片,由于TEM切片制备过程繁琐以及对整个切片集进行后续图像处理,因此劳动强度很大。在本章中,我们介绍了连续块面扫描电子显微镜,以及用于球体形成、细胞区室对比、图像处理和三维可视化的复杂方法。所描述的技术对于干细胞球体、类器官以及器官型细胞培养物的详细形态分析是有效的。