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Optical imaging of the small intestine immune compartment across scales
The limitations of 2D microscopy constrain our ability to observe and understand tissue-wide networks that are, by nature, 3-dimensional. Optical projection tomography (OPT) enables the acquisition of large volumes (ranging from micrometres to centimetres) in various tissues. We present a multi-moda...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10066397/ https://www.ncbi.nlm.nih.gov/pubmed/37002381 http://dx.doi.org/10.1038/s42003-023-04642-3 |
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author | Planchette, Arielle Louise Schmidt, Cédric Burri, Olivier Gomez de Agüero, Mercedes Radenovic, Aleksandra Mylonas, Alessio Extermann, Jérôme |
author_facet | Planchette, Arielle Louise Schmidt, Cédric Burri, Olivier Gomez de Agüero, Mercedes Radenovic, Aleksandra Mylonas, Alessio Extermann, Jérôme |
author_sort | Planchette, Arielle Louise |
collection | PubMed |
description | The limitations of 2D microscopy constrain our ability to observe and understand tissue-wide networks that are, by nature, 3-dimensional. Optical projection tomography (OPT) enables the acquisition of large volumes (ranging from micrometres to centimetres) in various tissues. We present a multi-modal workflow for the characterization of both structural and quantitative parameters of the mouse small intestine. As proof of principle, we evidence its applicability for imaging the mouse intestinal immune compartment and surrounding mucosal structures. We quantify the volumetric size and spatial distribution of Isolated Lymphoid Follicles (ILFs) and quantify the density of villi throughout centimetre-long segments of intestine. Furthermore, we exhibit the age and microbiota dependence for ILF development, and leverage a technique that we call reverse-OPT for identifying and homing in on regions of interest. Several quantification capabilities are displayed, including villous density in the autofluorescent channel and the size and spatial distribution of the signal of interest at millimetre-scale volumes. The concatenation of 3D imaging with reverse-OPT and high-resolution 2D imaging allows accurate localisation of ROIs and adds value to interpretations made in 3D. Importantly, OPT may be used to identify sparsely-distributed regions of interest in large volumes whilst retaining compatibility with high-resolution microscopy modalities, including confocal microscopy. We believe this pipeline to be approachable for a wide-range of specialties, and to provide a new method for characterisation of the mouse intestinal immune compartment. |
format | Online Article Text |
id | pubmed-10066397 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-100663972023-04-02 Optical imaging of the small intestine immune compartment across scales Planchette, Arielle Louise Schmidt, Cédric Burri, Olivier Gomez de Agüero, Mercedes Radenovic, Aleksandra Mylonas, Alessio Extermann, Jérôme Commun Biol Article The limitations of 2D microscopy constrain our ability to observe and understand tissue-wide networks that are, by nature, 3-dimensional. Optical projection tomography (OPT) enables the acquisition of large volumes (ranging from micrometres to centimetres) in various tissues. We present a multi-modal workflow for the characterization of both structural and quantitative parameters of the mouse small intestine. As proof of principle, we evidence its applicability for imaging the mouse intestinal immune compartment and surrounding mucosal structures. We quantify the volumetric size and spatial distribution of Isolated Lymphoid Follicles (ILFs) and quantify the density of villi throughout centimetre-long segments of intestine. Furthermore, we exhibit the age and microbiota dependence for ILF development, and leverage a technique that we call reverse-OPT for identifying and homing in on regions of interest. Several quantification capabilities are displayed, including villous density in the autofluorescent channel and the size and spatial distribution of the signal of interest at millimetre-scale volumes. The concatenation of 3D imaging with reverse-OPT and high-resolution 2D imaging allows accurate localisation of ROIs and adds value to interpretations made in 3D. Importantly, OPT may be used to identify sparsely-distributed regions of interest in large volumes whilst retaining compatibility with high-resolution microscopy modalities, including confocal microscopy. We believe this pipeline to be approachable for a wide-range of specialties, and to provide a new method for characterisation of the mouse intestinal immune compartment. Nature Publishing Group UK 2023-03-31 /pmc/articles/PMC10066397/ /pubmed/37002381 http://dx.doi.org/10.1038/s42003-023-04642-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Planchette, Arielle Louise Schmidt, Cédric Burri, Olivier Gomez de Agüero, Mercedes Radenovic, Aleksandra Mylonas, Alessio Extermann, Jérôme Optical imaging of the small intestine immune compartment across scales |
title | Optical imaging of the small intestine immune compartment across scales |
title_full | Optical imaging of the small intestine immune compartment across scales |
title_fullStr | Optical imaging of the small intestine immune compartment across scales |
title_full_unstemmed | Optical imaging of the small intestine immune compartment across scales |
title_short | Optical imaging of the small intestine immune compartment across scales |
title_sort | optical imaging of the small intestine immune compartment across scales |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10066397/ https://www.ncbi.nlm.nih.gov/pubmed/37002381 http://dx.doi.org/10.1038/s42003-023-04642-3 |
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