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Streamlined intravital imaging approach for long-term monitoring of epithelial tissue dynamics on an inverted confocal microscope
Understanding normal and aberrant in vivo cell behaviors is necessary to develop clinical interventions to thwart disease initiation and progression. It is therefore critical to optimize imaging approaches that facilitate the observation of cell dynamics in situ, where tissue structure and compositi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10197696/ https://www.ncbi.nlm.nih.gov/pubmed/37214899 http://dx.doi.org/10.1101/2023.05.10.540242 |
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author | Hamersky, Michael Tekale, Khushi Winfree, L. Matthew Rowan, Matthew JM Seldin, Lindsey |
author_facet | Hamersky, Michael Tekale, Khushi Winfree, L. Matthew Rowan, Matthew JM Seldin, Lindsey |
author_sort | Hamersky, Michael |
collection | PubMed |
description | Understanding normal and aberrant in vivo cell behaviors is necessary to develop clinical interventions to thwart disease initiation and progression. It is therefore critical to optimize imaging approaches that facilitate the observation of cell dynamics in situ, where tissue structure and composition remain unperturbed. The epidermis is the body’s outermost barrier as well as the source of the most prevalent human cancers, namely cutaneous skin carcinomas. The accessibility of skin tissue presents a unique opportunity to monitor epithelial and dermal cell behaviors in intact animals using noninvasive intravital microscopy. Nevertheless, this sophisticated imaging approach has primarily been achieved using upright multiphoton microscopes, which represents a significant barrierfor-entry for most investigators. In this study, we present a custom-designed 3D-printed microscope stage insert suitable for use with inverted confocal microscopes that streamlines long-term intravital imaging of ear skin in live transgenic mice. We believe this versatile invention, which may be customized to fit the inverted microscope brand and model of choice, as well as adapted to image additional organ systems, will prove invaluable to the greater scientific research community by significantly enhancing the accessibility of intravital microscopy. This technological advancement is critical to bolster our understanding of live cell dynamics in both normal and disease contexts. |
format | Online Article Text |
id | pubmed-10197696 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-101976962023-05-20 Streamlined intravital imaging approach for long-term monitoring of epithelial tissue dynamics on an inverted confocal microscope Hamersky, Michael Tekale, Khushi Winfree, L. Matthew Rowan, Matthew JM Seldin, Lindsey bioRxiv Article Understanding normal and aberrant in vivo cell behaviors is necessary to develop clinical interventions to thwart disease initiation and progression. It is therefore critical to optimize imaging approaches that facilitate the observation of cell dynamics in situ, where tissue structure and composition remain unperturbed. The epidermis is the body’s outermost barrier as well as the source of the most prevalent human cancers, namely cutaneous skin carcinomas. The accessibility of skin tissue presents a unique opportunity to monitor epithelial and dermal cell behaviors in intact animals using noninvasive intravital microscopy. Nevertheless, this sophisticated imaging approach has primarily been achieved using upright multiphoton microscopes, which represents a significant barrierfor-entry for most investigators. In this study, we present a custom-designed 3D-printed microscope stage insert suitable for use with inverted confocal microscopes that streamlines long-term intravital imaging of ear skin in live transgenic mice. We believe this versatile invention, which may be customized to fit the inverted microscope brand and model of choice, as well as adapted to image additional organ systems, will prove invaluable to the greater scientific research community by significantly enhancing the accessibility of intravital microscopy. This technological advancement is critical to bolster our understanding of live cell dynamics in both normal and disease contexts. Cold Spring Harbor Laboratory 2023-05-12 /pmc/articles/PMC10197696/ /pubmed/37214899 http://dx.doi.org/10.1101/2023.05.10.540242 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Hamersky, Michael Tekale, Khushi Winfree, L. Matthew Rowan, Matthew JM Seldin, Lindsey Streamlined intravital imaging approach for long-term monitoring of epithelial tissue dynamics on an inverted confocal microscope |
title | Streamlined intravital imaging approach for long-term monitoring of epithelial tissue dynamics on an inverted confocal microscope |
title_full | Streamlined intravital imaging approach for long-term monitoring of epithelial tissue dynamics on an inverted confocal microscope |
title_fullStr | Streamlined intravital imaging approach for long-term monitoring of epithelial tissue dynamics on an inverted confocal microscope |
title_full_unstemmed | Streamlined intravital imaging approach for long-term monitoring of epithelial tissue dynamics on an inverted confocal microscope |
title_short | Streamlined intravital imaging approach for long-term monitoring of epithelial tissue dynamics on an inverted confocal microscope |
title_sort | streamlined intravital imaging approach for long-term monitoring of epithelial tissue dynamics on an inverted confocal microscope |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10197696/ https://www.ncbi.nlm.nih.gov/pubmed/37214899 http://dx.doi.org/10.1101/2023.05.10.540242 |
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