Combined methods to evaluate human cells in muscle xenografts.

Xenotransplantation of human cells into immunodeficient mouse models is a very powerful tool and an essential step for the pre-clinical evaluation of therapeutic cell- and gene- based strategies. Here we describe an optimized protocol combining immunofluorescence and real-time quantitative PCR to bo...

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Main Authors: Mona Bensalah, Pierre Klein, Ingo Riederer, Soraya Chaouch, Laura Muraine, Wilson Savino, Gillian Sandra Butler-Browne, Capucine Trollet, Vincent Mouly, Anne Bigot, Elisa Negroni
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2019-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0211522
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spelling doaj-32a8b9a00887482aaa2d4e9b6a8a16b12021-03-03T20:42:15ZengPublic Library of Science (PLoS)PLoS ONE1932-62032019-01-01145e021152210.1371/journal.pone.0211522Combined methods to evaluate human cells in muscle xenografts.Mona BensalahPierre KleinIngo RiedererSoraya ChaouchLaura MuraineWilson SavinoGillian Sandra Butler-BrowneCapucine TrolletVincent MoulyAnne BigotElisa NegroniXenotransplantation of human cells into immunodeficient mouse models is a very powerful tool and an essential step for the pre-clinical evaluation of therapeutic cell- and gene- based strategies. Here we describe an optimized protocol combining immunofluorescence and real-time quantitative PCR to both quantify and visualize the fate and localization of human myogenic cells after injection in regenerating muscles of immunodeficient mice. Whereas real-time quantitative PCR-based method provides an accurate quantification of human cells, it does not document their specific localization. The addition of an immunofluorescence approach using human-specific antibodies recognizing engrafted human cells gives information on the localization of the human cells within the host muscle fibres, in the stem cell niche or in the interstitial space. These two combined approaches offer an accurate evaluation of human engraftment including cell number and localization and should provide a gold standard to compare results obtained either using different types of human stem cells or comparing healthy and pathological muscle stem cells between different research laboratories worldwide.https://doi.org/10.1371/journal.pone.0211522
collection DOAJ
language English
format Article
sources DOAJ
author Mona Bensalah
Pierre Klein
Ingo Riederer
Soraya Chaouch
Laura Muraine
Wilson Savino
Gillian Sandra Butler-Browne
Capucine Trollet
Vincent Mouly
Anne Bigot
Elisa Negroni
spellingShingle Mona Bensalah
Pierre Klein
Ingo Riederer
Soraya Chaouch
Laura Muraine
Wilson Savino
Gillian Sandra Butler-Browne
Capucine Trollet
Vincent Mouly
Anne Bigot
Elisa Negroni
Combined methods to evaluate human cells in muscle xenografts.
PLoS ONE
author_facet Mona Bensalah
Pierre Klein
Ingo Riederer
Soraya Chaouch
Laura Muraine
Wilson Savino
Gillian Sandra Butler-Browne
Capucine Trollet
Vincent Mouly
Anne Bigot
Elisa Negroni
author_sort Mona Bensalah
title Combined methods to evaluate human cells in muscle xenografts.
title_short Combined methods to evaluate human cells in muscle xenografts.
title_full Combined methods to evaluate human cells in muscle xenografts.
title_fullStr Combined methods to evaluate human cells in muscle xenografts.
title_full_unstemmed Combined methods to evaluate human cells in muscle xenografts.
title_sort combined methods to evaluate human cells in muscle xenografts.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2019-01-01
description Xenotransplantation of human cells into immunodeficient mouse models is a very powerful tool and an essential step for the pre-clinical evaluation of therapeutic cell- and gene- based strategies. Here we describe an optimized protocol combining immunofluorescence and real-time quantitative PCR to both quantify and visualize the fate and localization of human myogenic cells after injection in regenerating muscles of immunodeficient mice. Whereas real-time quantitative PCR-based method provides an accurate quantification of human cells, it does not document their specific localization. The addition of an immunofluorescence approach using human-specific antibodies recognizing engrafted human cells gives information on the localization of the human cells within the host muscle fibres, in the stem cell niche or in the interstitial space. These two combined approaches offer an accurate evaluation of human engraftment including cell number and localization and should provide a gold standard to compare results obtained either using different types of human stem cells or comparing healthy and pathological muscle stem cells between different research laboratories worldwide.
url https://doi.org/10.1371/journal.pone.0211522
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