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High-resolution 3D imaging of whole organ after clearing: taking a new look at the zebrafish testis
Zebrafish testis has become a powerful model for reproductive biology of teleostean fishes and other vertebrates and encompasses multiple applications in applied and basic research. Many studies have focused on 2D images, which is time consuming and implies extrapolation of results. Three-dimensiona...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5314416/ https://www.ncbi.nlm.nih.gov/pubmed/28211501 http://dx.doi.org/10.1038/srep43012 |
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author | Frétaud, Maxence Rivière, Laurie Job, Élodie De Gay, Stéphanie Lareyre, Jean-Jacques Joly, Jean-Stéphane Affaticati, Pierre Thermes, Violette |
author_facet | Frétaud, Maxence Rivière, Laurie Job, Élodie De Gay, Stéphanie Lareyre, Jean-Jacques Joly, Jean-Stéphane Affaticati, Pierre Thermes, Violette |
author_sort | Frétaud, Maxence |
collection | PubMed |
description | Zebrafish testis has become a powerful model for reproductive biology of teleostean fishes and other vertebrates and encompasses multiple applications in applied and basic research. Many studies have focused on 2D images, which is time consuming and implies extrapolation of results. Three-dimensional imaging of whole organs recently became an important challenge to better understand their architecture and allow cell enumeration. Several protocols have thus been developed to enhance sample transparency, a limiting step for imaging large biological samples. However, none of these methods has been applied to the zebrafish testis. We tested five clearing protocols to determine if some of them could be applied with only small modifications to the testis. We compared clearing efficiency at both macroscopic and microscopic levels. CUBIC and PACT were suitable for an efficient transparency, an optimal optical penetration, the GFP fluorescence preservation and avoiding meaningful tissue deformation. Finally, we succeeded in whole testis 3D capture at a cellular resolution with both CUBIC and PACT, which will be valuable in a standard workflow to investigate the 3D architecture of the testis and its cellular content. This paves the way for further development of high content phenotyping studies in several fields including development, genetic or toxicology. |
format | Online Article Text |
id | pubmed-5314416 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53144162017-02-24 High-resolution 3D imaging of whole organ after clearing: taking a new look at the zebrafish testis Frétaud, Maxence Rivière, Laurie Job, Élodie De Gay, Stéphanie Lareyre, Jean-Jacques Joly, Jean-Stéphane Affaticati, Pierre Thermes, Violette Sci Rep Article Zebrafish testis has become a powerful model for reproductive biology of teleostean fishes and other vertebrates and encompasses multiple applications in applied and basic research. Many studies have focused on 2D images, which is time consuming and implies extrapolation of results. Three-dimensional imaging of whole organs recently became an important challenge to better understand their architecture and allow cell enumeration. Several protocols have thus been developed to enhance sample transparency, a limiting step for imaging large biological samples. However, none of these methods has been applied to the zebrafish testis. We tested five clearing protocols to determine if some of them could be applied with only small modifications to the testis. We compared clearing efficiency at both macroscopic and microscopic levels. CUBIC and PACT were suitable for an efficient transparency, an optimal optical penetration, the GFP fluorescence preservation and avoiding meaningful tissue deformation. Finally, we succeeded in whole testis 3D capture at a cellular resolution with both CUBIC and PACT, which will be valuable in a standard workflow to investigate the 3D architecture of the testis and its cellular content. This paves the way for further development of high content phenotyping studies in several fields including development, genetic or toxicology. Nature Publishing Group 2017-02-17 /pmc/articles/PMC5314416/ /pubmed/28211501 http://dx.doi.org/10.1038/srep43012 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Frétaud, Maxence Rivière, Laurie Job, Élodie De Gay, Stéphanie Lareyre, Jean-Jacques Joly, Jean-Stéphane Affaticati, Pierre Thermes, Violette High-resolution 3D imaging of whole organ after clearing: taking a new look at the zebrafish testis |
title | High-resolution 3D imaging of whole organ after clearing: taking a new look at the zebrafish testis |
title_full | High-resolution 3D imaging of whole organ after clearing: taking a new look at the zebrafish testis |
title_fullStr | High-resolution 3D imaging of whole organ after clearing: taking a new look at the zebrafish testis |
title_full_unstemmed | High-resolution 3D imaging of whole organ after clearing: taking a new look at the zebrafish testis |
title_short | High-resolution 3D imaging of whole organ after clearing: taking a new look at the zebrafish testis |
title_sort | high-resolution 3d imaging of whole organ after clearing: taking a new look at the zebrafish testis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5314416/ https://www.ncbi.nlm.nih.gov/pubmed/28211501 http://dx.doi.org/10.1038/srep43012 |
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