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Routine Optical Clearing of 3D-Cell Cultures: Simplicity Forward
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, tiss...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7046628/ https://www.ncbi.nlm.nih.gov/pubmed/32154265 http://dx.doi.org/10.3389/fmolb.2020.00020 |
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author | 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 |
author_facet | 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 |
author_sort | Nürnberg, Elina |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-7046628 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-70466282020-03-09 Routine Optical Clearing of 3D-Cell Cultures: Simplicity Forward 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 Front Mol Biosci Molecular Biosciences 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. Frontiers Media S.A. 2020-02-21 /pmc/articles/PMC7046628/ /pubmed/32154265 http://dx.doi.org/10.3389/fmolb.2020.00020 Text en Copyright © 2020 Nürnberg, Vitacolonna, Klicks, von Molitor, Cesetti, Keller, Bruch, Ertongur-Fauth, Riedel, Scholz, Lau, Schneider, Meier, Hafner and Rudolf. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Molecular Biosciences 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 Routine Optical Clearing of 3D-Cell Cultures: Simplicity Forward |
title | Routine Optical Clearing of 3D-Cell Cultures: Simplicity Forward |
title_full | Routine Optical Clearing of 3D-Cell Cultures: Simplicity Forward |
title_fullStr | Routine Optical Clearing of 3D-Cell Cultures: Simplicity Forward |
title_full_unstemmed | Routine Optical Clearing of 3D-Cell Cultures: Simplicity Forward |
title_short | Routine Optical Clearing of 3D-Cell Cultures: Simplicity Forward |
title_sort | routine optical clearing of 3d-cell cultures: simplicity forward |
topic | Molecular Biosciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7046628/ https://www.ncbi.nlm.nih.gov/pubmed/32154265 http://dx.doi.org/10.3389/fmolb.2020.00020 |
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