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Studying exogenous extracellular vesicle biodistribution by in vivo fluorescence microscopy

Extracellular vesicles (EVs) are lipid-bound vesicles released from cells that play a crucial role in many physiological processes and pathological mechanisms. As such, there is great interest in their biodistribution. One currently accessible technology to study their fate in vivo involves fluoresc...

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Autores principales: Lau, Sien Yee, Kang, Matthew, Hisey, Colin L., Chamley, Lawrence W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10417515/
https://www.ncbi.nlm.nih.gov/pubmed/37526034
http://dx.doi.org/10.1242/dmm.050074
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author Lau, Sien Yee
Kang, Matthew
Hisey, Colin L.
Chamley, Lawrence W.
author_facet Lau, Sien Yee
Kang, Matthew
Hisey, Colin L.
Chamley, Lawrence W.
author_sort Lau, Sien Yee
collection PubMed
description Extracellular vesicles (EVs) are lipid-bound vesicles released from cells that play a crucial role in many physiological processes and pathological mechanisms. As such, there is great interest in their biodistribution. One currently accessible technology to study their fate in vivo involves fluorescent labelling of exogenous EVs followed by whole-animal imaging. Although this is not a new technology, its translation from studying the fate of whole cells to subcellular EVs requires adaptation of the labelling techniques, excess dye removal and a refined experimental design. In this Review, we detail the methods and considerations for using fluorescence in vivo and ex vivo imaging to study the biodistribution of exogenous EVs and their roles in physiology and disease biology.
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spelling pubmed-104175152023-08-12 Studying exogenous extracellular vesicle biodistribution by in vivo fluorescence microscopy Lau, Sien Yee Kang, Matthew Hisey, Colin L. Chamley, Lawrence W. Dis Model Mech Review Extracellular vesicles (EVs) are lipid-bound vesicles released from cells that play a crucial role in many physiological processes and pathological mechanisms. As such, there is great interest in their biodistribution. One currently accessible technology to study their fate in vivo involves fluorescent labelling of exogenous EVs followed by whole-animal imaging. Although this is not a new technology, its translation from studying the fate of whole cells to subcellular EVs requires adaptation of the labelling techniques, excess dye removal and a refined experimental design. In this Review, we detail the methods and considerations for using fluorescence in vivo and ex vivo imaging to study the biodistribution of exogenous EVs and their roles in physiology and disease biology. The Company of Biologists Ltd 2023-08-01 /pmc/articles/PMC10417515/ /pubmed/37526034 http://dx.doi.org/10.1242/dmm.050074 Text en © 2023. Published by The Company of Biologists Ltd https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Review
Lau, Sien Yee
Kang, Matthew
Hisey, Colin L.
Chamley, Lawrence W.
Studying exogenous extracellular vesicle biodistribution by in vivo fluorescence microscopy
title Studying exogenous extracellular vesicle biodistribution by in vivo fluorescence microscopy
title_full Studying exogenous extracellular vesicle biodistribution by in vivo fluorescence microscopy
title_fullStr Studying exogenous extracellular vesicle biodistribution by in vivo fluorescence microscopy
title_full_unstemmed Studying exogenous extracellular vesicle biodistribution by in vivo fluorescence microscopy
title_short Studying exogenous extracellular vesicle biodistribution by in vivo fluorescence microscopy
title_sort studying exogenous extracellular vesicle biodistribution by in vivo fluorescence microscopy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10417515/
https://www.ncbi.nlm.nih.gov/pubmed/37526034
http://dx.doi.org/10.1242/dmm.050074
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