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Foreskin-derived mesenchymal stromal cells with aldehyde dehydrogenase activity: isolation and gene profiling

BACKGROUND: Mesenchymal stromal cells (MSCs) become an attractive research topic because of their crucial roles in tissue repair and regenerative medicine. Foreskin is considered as a valuable tissue source containing immunotherapeutic MSCs (FSK-MSCs). RESULTS: In this work, we used aldehyde dehydro...

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Autores principales: Najar, Mehdi, Crompot, Emerence, van Grunsven, Leo A., Dollé, Laurent, Lagneaux, Laurence
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5889569/
https://www.ncbi.nlm.nih.gov/pubmed/29625551
http://dx.doi.org/10.1186/s12860-018-0157-0
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author Najar, Mehdi
Crompot, Emerence
van Grunsven, Leo A.
Dollé, Laurent
Lagneaux, Laurence
author_facet Najar, Mehdi
Crompot, Emerence
van Grunsven, Leo A.
Dollé, Laurent
Lagneaux, Laurence
author_sort Najar, Mehdi
collection PubMed
description BACKGROUND: Mesenchymal stromal cells (MSCs) become an attractive research topic because of their crucial roles in tissue repair and regenerative medicine. Foreskin is considered as a valuable tissue source containing immunotherapeutic MSCs (FSK-MSCs). RESULTS: In this work, we used aldehyde dehydrogenase activity (ALDH) assay (ALDEFLUOR™) to isolate and therefore characterize subsets of FSK-MSCs. According to their ALDH activity, we were able to distinguish and sort by fluorescence activated cell sorting (FACS) two subsets of FSK-MSCs (referred as ALDH(+) and ALDH(−)). Consequently, these subsets were characterized by profiling the gene expression related to the main properties of MSCs (proliferation, response to hypoxia, angiogenesis, phenotype, stemness, multilineage, hematopoiesis and immunomodulation). We thus demonstrated by Real Time PCR several relevant differences in gene expression based on their ALDH activity. CONCLUSION: Taken together, this preliminary study suggests that distinct subsets of FSK-MSCs with differential gene expression profiles depending of ALDH activity could be identified. These populations could differ in terms of biological functionalities involving the selection by ALDH activity as useful tool for potent therapeutic applications. However, functional studies should be conducted to confirm their therapeutic relevance. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12860-018-0157-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-58895692018-04-10 Foreskin-derived mesenchymal stromal cells with aldehyde dehydrogenase activity: isolation and gene profiling Najar, Mehdi Crompot, Emerence van Grunsven, Leo A. Dollé, Laurent Lagneaux, Laurence BMC Cell Biol Methodology Article BACKGROUND: Mesenchymal stromal cells (MSCs) become an attractive research topic because of their crucial roles in tissue repair and regenerative medicine. Foreskin is considered as a valuable tissue source containing immunotherapeutic MSCs (FSK-MSCs). RESULTS: In this work, we used aldehyde dehydrogenase activity (ALDH) assay (ALDEFLUOR™) to isolate and therefore characterize subsets of FSK-MSCs. According to their ALDH activity, we were able to distinguish and sort by fluorescence activated cell sorting (FACS) two subsets of FSK-MSCs (referred as ALDH(+) and ALDH(−)). Consequently, these subsets were characterized by profiling the gene expression related to the main properties of MSCs (proliferation, response to hypoxia, angiogenesis, phenotype, stemness, multilineage, hematopoiesis and immunomodulation). We thus demonstrated by Real Time PCR several relevant differences in gene expression based on their ALDH activity. CONCLUSION: Taken together, this preliminary study suggests that distinct subsets of FSK-MSCs with differential gene expression profiles depending of ALDH activity could be identified. These populations could differ in terms of biological functionalities involving the selection by ALDH activity as useful tool for potent therapeutic applications. However, functional studies should be conducted to confirm their therapeutic relevance. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12860-018-0157-0) contains supplementary material, which is available to authorized users. BioMed Central 2018-04-06 /pmc/articles/PMC5889569/ /pubmed/29625551 http://dx.doi.org/10.1186/s12860-018-0157-0 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Methodology Article
Najar, Mehdi
Crompot, Emerence
van Grunsven, Leo A.
Dollé, Laurent
Lagneaux, Laurence
Foreskin-derived mesenchymal stromal cells with aldehyde dehydrogenase activity: isolation and gene profiling
title Foreskin-derived mesenchymal stromal cells with aldehyde dehydrogenase activity: isolation and gene profiling
title_full Foreskin-derived mesenchymal stromal cells with aldehyde dehydrogenase activity: isolation and gene profiling
title_fullStr Foreskin-derived mesenchymal stromal cells with aldehyde dehydrogenase activity: isolation and gene profiling
title_full_unstemmed Foreskin-derived mesenchymal stromal cells with aldehyde dehydrogenase activity: isolation and gene profiling
title_short Foreskin-derived mesenchymal stromal cells with aldehyde dehydrogenase activity: isolation and gene profiling
title_sort foreskin-derived mesenchymal stromal cells with aldehyde dehydrogenase activity: isolation and gene profiling
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5889569/
https://www.ncbi.nlm.nih.gov/pubmed/29625551
http://dx.doi.org/10.1186/s12860-018-0157-0
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