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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...

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Autores principales: Hamersky, Michael, Tekale, Khushi, Winfree, L. Matthew, Rowan, Matthew JM, Seldin, Lindsey
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
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.
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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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