Nürnberg Elina, Vitacolonna Mario, Klicks Julia, von Molitor Elena, Cesetti Tiziana, Keller Florian, Bruch Roman, Ertongur-Fauth Torsten, Riedel Katja, Scholz Paul, Lau Thorsten, Schneider Richard, Meier Julia, Hafner Mathias, Rudolf Rüdiger
Institute of Molecular and Cell Biology, Faculty of Biotechnology, Mannheim University of Applied Sciences, Mannheim, Germany.
Zentralinstitut für Seelische Gesundheit, Department of Translational Brain Research, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.
Front Mol Biosci. 2020 Feb 21;7:20. doi: 10.3389/fmolb.2020.00020. eCollection 2020.
Three-dimensional cell cultures, such as spheroids and organoids, serve as increasingly important models in fundamental and applied research and start to be used for drug screening purposes. Optical tissue clearing procedures are employed to enhance visualization of fluorescence-stained organs, tissues, and three-dimensional cell cultures. To get a more systematic overview about the effects and applicability of optical tissue clearing on three-dimensional cell cultures, we compared six different clearing/embedding protocols on seven types of spheroid- and chip-based three-dimensional cell cultures of approximately 300 μm in size that were stained with nuclear dyes, immunofluorescence, cell trackers, and cyan fluorescent protein. Subsequent whole mount confocal microscopy and semi-automated image analysis were performed to quantify the effects. Quantitative analysis included fluorescence signal intensity and signal-to-noise ratio as a function of z-depth as well as segmentation and counting of nuclei and immunopositive cells. In general, these analyses revealed five key points, which largely confirmed current knowledge and were quantified in this study. First, there was a massive variability of effects of different clearing protocols on sample transparency and shrinkage as well as on dye quenching. Second, all tested clearing protocols worked more efficiently on samples prepared with one cell type than on co-cultures. Third, z-compensation was imperative to minimize variations in signal-to-noise ratio. Fourth, a combination of sample-inherent cell density, sample shrinkage, uniformity of signal-to-noise ratio, and image resolution had a strong impact on data segmentation, cell counts, and relative numbers of immunofluorescence-positive cells. Finally, considering all mentioned aspects and including a wish for simplicity and speed of protocols - in particular, for screening purposes - clearing with 88% Glycerol appeared to be the most promising option amongst the ones tested.
三维细胞培养,如球体和类器官,在基础研究和应用研究中作为越来越重要的模型,并开始用于药物筛选目的。光学组织透明化程序用于增强对荧光染色的器官、组织和三维细胞培养的可视化。为了更系统地了解光学组织透明化对三维细胞培养的影响和适用性,我们比较了六种不同的透明化/包埋方案,这些方案应用于七种基于球体和芯片的三维细胞培养物,其大小约为300μm,用核染料、免疫荧光、细胞追踪剂和青色荧光蛋白进行了染色。随后进行了全组织共聚焦显微镜检查和半自动图像分析以量化这些影响。定量分析包括荧光信号强度和信噪比作为z深度的函数,以及细胞核和免疫阳性细胞的分割和计数。总体而言,这些分析揭示了五个关键点,这些关键点在很大程度上证实了现有知识并在本研究中进行了量化。第一,不同透明化方案对样品透明度、收缩以及染料淬灭的影响存在巨大差异。第二,所有测试的透明化方案在单一细胞类型制备的样品上比在共培养物上更有效。第三,z补偿对于最小化信噪比的变化至关重要。第四,样品固有的细胞密度、样品收缩、信噪比的均匀性和图像分辨率的组合对数据分割、细胞计数以及免疫荧光阳性细胞的相对数量有强烈影响。最后,考虑到所有上述方面,并包括对方案简单性和速度的期望——特别是对于筛选目的——88%甘油透明化似乎是测试方案中最有前景的选择。