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Bioluminescence-mediated longitudinal monitoring of adipose-derived stem cells in a large mammal ex vivo organ culture

Recently, ex vivo three-dimensional organ culture systems have emerged to study the physiology and pathophysiology of human organs. These systems also have potential as a translational tool in tissue engineering; however, this potential is limited by our ability to longitudinally monitor the fate an...

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Autores principales: Peeters, Mirte, van Rijn, Sjoerd, Vergroesen, Pieter-Paul A., Paul, Cornelis P. L., Noske, David P., Peter Vandertop, W., Wurdinger, Thomas, Helder, Marco N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4563666/
https://www.ncbi.nlm.nih.gov/pubmed/26350622
http://dx.doi.org/10.1038/srep13960
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author Peeters, Mirte
van Rijn, Sjoerd
Vergroesen, Pieter-Paul A.
Paul, Cornelis P. L.
Noske, David P.
Peter Vandertop, W.
Wurdinger, Thomas
Helder, Marco N.
author_facet Peeters, Mirte
van Rijn, Sjoerd
Vergroesen, Pieter-Paul A.
Paul, Cornelis P. L.
Noske, David P.
Peter Vandertop, W.
Wurdinger, Thomas
Helder, Marco N.
author_sort Peeters, Mirte
collection PubMed
description Recently, ex vivo three-dimensional organ culture systems have emerged to study the physiology and pathophysiology of human organs. These systems also have potential as a translational tool in tissue engineering; however, this potential is limited by our ability to longitudinally monitor the fate and action of cells used in regenerative therapies. Therefore, we investigated luciferase-mediated bioluminescence imaging (BLI) as a non-invasive technique to continuously monitor cellular behavior in ex vivo whole organ culture. Goat adipose-derived stem cells (gADSCs) were transduced with either Firefly luciferase (Fluc) or Gaussia luciferase (Gluc) reporter genes and injected in isolated goat intervertebral discs (IVD). Luciferase activity was monitored by BLI for at least seven days of culture. Additionally, possible confounders specific to avascular organ culture were investigated. Gluc imaging proved to be more suitable compared to Fluc in monitoring gADSCs in goat IVDs. We conclude that BLI is a promising tool to monitor spatial and temporal cellular behavior in ex vivo organ culture. Hence, ex vivo organ culture systems allow pre-screening and pre-validation of novel therapeutic concepts prior to in vivo large animal experimentation. Thereby, organ culture systems can reduce animal use, and improve the speed of innovation by overcoming technological, ethical and financial challenges.
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spelling pubmed-45636662015-09-15 Bioluminescence-mediated longitudinal monitoring of adipose-derived stem cells in a large mammal ex vivo organ culture Peeters, Mirte van Rijn, Sjoerd Vergroesen, Pieter-Paul A. Paul, Cornelis P. L. Noske, David P. Peter Vandertop, W. Wurdinger, Thomas Helder, Marco N. Sci Rep Article Recently, ex vivo three-dimensional organ culture systems have emerged to study the physiology and pathophysiology of human organs. These systems also have potential as a translational tool in tissue engineering; however, this potential is limited by our ability to longitudinally monitor the fate and action of cells used in regenerative therapies. Therefore, we investigated luciferase-mediated bioluminescence imaging (BLI) as a non-invasive technique to continuously monitor cellular behavior in ex vivo whole organ culture. Goat adipose-derived stem cells (gADSCs) were transduced with either Firefly luciferase (Fluc) or Gaussia luciferase (Gluc) reporter genes and injected in isolated goat intervertebral discs (IVD). Luciferase activity was monitored by BLI for at least seven days of culture. Additionally, possible confounders specific to avascular organ culture were investigated. Gluc imaging proved to be more suitable compared to Fluc in monitoring gADSCs in goat IVDs. We conclude that BLI is a promising tool to monitor spatial and temporal cellular behavior in ex vivo organ culture. Hence, ex vivo organ culture systems allow pre-screening and pre-validation of novel therapeutic concepts prior to in vivo large animal experimentation. Thereby, organ culture systems can reduce animal use, and improve the speed of innovation by overcoming technological, ethical and financial challenges. Nature Publishing Group 2015-09-09 /pmc/articles/PMC4563666/ /pubmed/26350622 http://dx.doi.org/10.1038/srep13960 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Peeters, Mirte
van Rijn, Sjoerd
Vergroesen, Pieter-Paul A.
Paul, Cornelis P. L.
Noske, David P.
Peter Vandertop, W.
Wurdinger, Thomas
Helder, Marco N.
Bioluminescence-mediated longitudinal monitoring of adipose-derived stem cells in a large mammal ex vivo organ culture
title Bioluminescence-mediated longitudinal monitoring of adipose-derived stem cells in a large mammal ex vivo organ culture
title_full Bioluminescence-mediated longitudinal monitoring of adipose-derived stem cells in a large mammal ex vivo organ culture
title_fullStr Bioluminescence-mediated longitudinal monitoring of adipose-derived stem cells in a large mammal ex vivo organ culture
title_full_unstemmed Bioluminescence-mediated longitudinal monitoring of adipose-derived stem cells in a large mammal ex vivo organ culture
title_short Bioluminescence-mediated longitudinal monitoring of adipose-derived stem cells in a large mammal ex vivo organ culture
title_sort bioluminescence-mediated longitudinal monitoring of adipose-derived stem cells in a large mammal ex vivo organ culture
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4563666/
https://www.ncbi.nlm.nih.gov/pubmed/26350622
http://dx.doi.org/10.1038/srep13960
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