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From 2D to 3D: Promising Advances in Imaging Lung Structure
The delicate structure of murine lungs poses many challenges for acquiring high-quality images that truly represent the living lung. Here, we describe several optimized procedures for obtaining and imaging murine lung tissue. Compared to traditional paraffin cross-section and optimal cutting tempera...
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/PMC7381109/ https://www.ncbi.nlm.nih.gov/pubmed/32766264 http://dx.doi.org/10.3389/fmed.2020.00343 |
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author | Klouda, Timothy Condon, David Hao, Yuan Tian, Wen Lvova, Maria Chakraborty, Ananya Nicolls, Mark R. Zhou, Xiaobo Raby, Benjamin A. Yuan, Ke |
author_facet | Klouda, Timothy Condon, David Hao, Yuan Tian, Wen Lvova, Maria Chakraborty, Ananya Nicolls, Mark R. Zhou, Xiaobo Raby, Benjamin A. Yuan, Ke |
author_sort | Klouda, Timothy |
collection | PubMed |
description | The delicate structure of murine lungs poses many challenges for acquiring high-quality images that truly represent the living lung. Here, we describe several optimized procedures for obtaining and imaging murine lung tissue. Compared to traditional paraffin cross-section and optimal cutting temperature (OCT), agarose-inflated vibratome sections (aka precision-cut lung slices), combines comparable structural preservation with experimental flexibility. In particular, we discuss an optimized procedure to precision-cut lung slices that can be used to visualize three-dimensional cell-cell interactions beyond the limitations of two-dimensional imaging. Super-resolution microscopy can then be used to reveal the fine structure of lung tissue's cellular bodies and processes that regular confocal cannot. Lastly, we evaluate the entire lung vasculature with clearing technology that allows imaging of the entire volume of the lung without sectioning. In this manuscript, we combine the above procedures to create a novel and evolutionary method to study cell behavior ex vivo, trace and reconstruct pulmonary vasculature, address fundamental questions relevant to a wide variety of vascular disorders, and perceive implications to better imaging clinical tissue. |
format | Online Article Text |
id | pubmed-7381109 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-73811092020-08-05 From 2D to 3D: Promising Advances in Imaging Lung Structure Klouda, Timothy Condon, David Hao, Yuan Tian, Wen Lvova, Maria Chakraborty, Ananya Nicolls, Mark R. Zhou, Xiaobo Raby, Benjamin A. Yuan, Ke Front Med (Lausanne) Medicine The delicate structure of murine lungs poses many challenges for acquiring high-quality images that truly represent the living lung. Here, we describe several optimized procedures for obtaining and imaging murine lung tissue. Compared to traditional paraffin cross-section and optimal cutting temperature (OCT), agarose-inflated vibratome sections (aka precision-cut lung slices), combines comparable structural preservation with experimental flexibility. In particular, we discuss an optimized procedure to precision-cut lung slices that can be used to visualize three-dimensional cell-cell interactions beyond the limitations of two-dimensional imaging. Super-resolution microscopy can then be used to reveal the fine structure of lung tissue's cellular bodies and processes that regular confocal cannot. Lastly, we evaluate the entire lung vasculature with clearing technology that allows imaging of the entire volume of the lung without sectioning. In this manuscript, we combine the above procedures to create a novel and evolutionary method to study cell behavior ex vivo, trace and reconstruct pulmonary vasculature, address fundamental questions relevant to a wide variety of vascular disorders, and perceive implications to better imaging clinical tissue. Frontiers Media S.A. 2020-07-16 /pmc/articles/PMC7381109/ /pubmed/32766264 http://dx.doi.org/10.3389/fmed.2020.00343 Text en Copyright © 2020 Klouda, Condon, Hao, Tian, Lvova, Chakraborty, Nicolls, Zhou, Raby and Yuan. 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 | Medicine Klouda, Timothy Condon, David Hao, Yuan Tian, Wen Lvova, Maria Chakraborty, Ananya Nicolls, Mark R. Zhou, Xiaobo Raby, Benjamin A. Yuan, Ke From 2D to 3D: Promising Advances in Imaging Lung Structure |
title | From 2D to 3D: Promising Advances in Imaging Lung Structure |
title_full | From 2D to 3D: Promising Advances in Imaging Lung Structure |
title_fullStr | From 2D to 3D: Promising Advances in Imaging Lung Structure |
title_full_unstemmed | From 2D to 3D: Promising Advances in Imaging Lung Structure |
title_short | From 2D to 3D: Promising Advances in Imaging Lung Structure |
title_sort | from 2d to 3d: promising advances in imaging lung structure |
topic | Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7381109/ https://www.ncbi.nlm.nih.gov/pubmed/32766264 http://dx.doi.org/10.3389/fmed.2020.00343 |
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