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In Vivo Tracking of Murine Adipose Tissue-Derived Multipotent Adult Stem Cells and Ex Vivo Cross-Validation
Stem cells are characterized by the ability to renew themselves and to differentiate into specialized cell types, while stem cell therapy is believed to treat a number of different human diseases through either cell regeneration or paracrine effects. Herein, an in vivo and ex vivo near infrared time...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3562659/ https://www.ncbi.nlm.nih.gov/pubmed/23401767 http://dx.doi.org/10.1155/2013/426961 |
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author | Garrovo, Chiara Bergamin, Natascha Bates, Dave Cesselli, Daniela Beltrami, Antonio Paolo Lorenzon, Andrea Ferrari, Roberto Alberto Beltrami, Carlo Lorusso, Vito Biffi, Stefania |
author_facet | Garrovo, Chiara Bergamin, Natascha Bates, Dave Cesselli, Daniela Beltrami, Antonio Paolo Lorenzon, Andrea Ferrari, Roberto Alberto Beltrami, Carlo Lorusso, Vito Biffi, Stefania |
author_sort | Garrovo, Chiara |
collection | PubMed |
description | Stem cells are characterized by the ability to renew themselves and to differentiate into specialized cell types, while stem cell therapy is believed to treat a number of different human diseases through either cell regeneration or paracrine effects. Herein, an in vivo and ex vivo near infrared time domain (NIR TD) optical imaging study was undertaken to evaluate the migratory ability of murine adipose tissue-derived multipotent adult stem cells [mAT-MASC] after intramuscular injection in mice. In vivo NIR TD optical imaging data analysis showed a migration of DiD-labelled mAT-MASC in the leg opposite the injection site, which was confirmed by a fibered confocal microendoscopy system. Ex vivo NIR TD optical imaging results showed a systemic distribution of labelled cells. Considering a potential microenvironmental contamination, a cross-validation study by multimodality approaches was followed: mAT-MASC were isolated from male mice expressing constitutively eGFP, which was detectable using techniques of immunofluorescence and qPCR. Y-chromosome positive cells, injected into wild-type female recipients, were detected by FISH. Cross-validation confirmed the data obtained by in vivo/ex vivo TD optical imaging analysis. In summary, our data demonstrates the usefulness of NIR TD optical imaging in tracking delivered cells, giving insights into the migratory properties of the injected cells. |
format | Online Article Text |
id | pubmed-3562659 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-35626592013-02-11 In Vivo Tracking of Murine Adipose Tissue-Derived Multipotent Adult Stem Cells and Ex Vivo Cross-Validation Garrovo, Chiara Bergamin, Natascha Bates, Dave Cesselli, Daniela Beltrami, Antonio Paolo Lorenzon, Andrea Ferrari, Roberto Alberto Beltrami, Carlo Lorusso, Vito Biffi, Stefania Int J Mol Imaging Research Article Stem cells are characterized by the ability to renew themselves and to differentiate into specialized cell types, while stem cell therapy is believed to treat a number of different human diseases through either cell regeneration or paracrine effects. Herein, an in vivo and ex vivo near infrared time domain (NIR TD) optical imaging study was undertaken to evaluate the migratory ability of murine adipose tissue-derived multipotent adult stem cells [mAT-MASC] after intramuscular injection in mice. In vivo NIR TD optical imaging data analysis showed a migration of DiD-labelled mAT-MASC in the leg opposite the injection site, which was confirmed by a fibered confocal microendoscopy system. Ex vivo NIR TD optical imaging results showed a systemic distribution of labelled cells. Considering a potential microenvironmental contamination, a cross-validation study by multimodality approaches was followed: mAT-MASC were isolated from male mice expressing constitutively eGFP, which was detectable using techniques of immunofluorescence and qPCR. Y-chromosome positive cells, injected into wild-type female recipients, were detected by FISH. Cross-validation confirmed the data obtained by in vivo/ex vivo TD optical imaging analysis. In summary, our data demonstrates the usefulness of NIR TD optical imaging in tracking delivered cells, giving insights into the migratory properties of the injected cells. Hindawi Publishing Corporation 2013 2013-01-17 /pmc/articles/PMC3562659/ /pubmed/23401767 http://dx.doi.org/10.1155/2013/426961 Text en Copyright © 2013 Chiara Garrovo et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Garrovo, Chiara Bergamin, Natascha Bates, Dave Cesselli, Daniela Beltrami, Antonio Paolo Lorenzon, Andrea Ferrari, Roberto Alberto Beltrami, Carlo Lorusso, Vito Biffi, Stefania In Vivo Tracking of Murine Adipose Tissue-Derived Multipotent Adult Stem Cells and Ex Vivo Cross-Validation |
title |
In Vivo Tracking of Murine Adipose Tissue-Derived Multipotent Adult Stem Cells and Ex Vivo Cross-Validation |
title_full |
In Vivo Tracking of Murine Adipose Tissue-Derived Multipotent Adult Stem Cells and Ex Vivo Cross-Validation |
title_fullStr |
In Vivo Tracking of Murine Adipose Tissue-Derived Multipotent Adult Stem Cells and Ex Vivo Cross-Validation |
title_full_unstemmed |
In Vivo Tracking of Murine Adipose Tissue-Derived Multipotent Adult Stem Cells and Ex Vivo Cross-Validation |
title_short |
In Vivo Tracking of Murine Adipose Tissue-Derived Multipotent Adult Stem Cells and Ex Vivo Cross-Validation |
title_sort | in vivo tracking of murine adipose tissue-derived multipotent adult stem cells and ex vivo cross-validation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3562659/ https://www.ncbi.nlm.nih.gov/pubmed/23401767 http://dx.doi.org/10.1155/2013/426961 |
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