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CD146/MCAM defines functionality of human bone marrow stromal stem cell populations
BACKGROUND: Identification of surface markers for prospective isolation of functionally homogenous populations of human skeletal (stromal, mesenchymal) stem cells (hMSCs) is highly relevant for cell therapy protocols. Thus, we examined the possible use of CD146 to subtype a heterogeneous hMSC popula...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4710006/ https://www.ncbi.nlm.nih.gov/pubmed/26753846 http://dx.doi.org/10.1186/s13287-015-0266-z |
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author | Harkness, Linda Zaher, Walid Ditzel, Nicholas Isa, Adiba Kassem, Moustapha |
author_facet | Harkness, Linda Zaher, Walid Ditzel, Nicholas Isa, Adiba Kassem, Moustapha |
author_sort | Harkness, Linda |
collection | PubMed |
description | BACKGROUND: Identification of surface markers for prospective isolation of functionally homogenous populations of human skeletal (stromal, mesenchymal) stem cells (hMSCs) is highly relevant for cell therapy protocols. Thus, we examined the possible use of CD146 to subtype a heterogeneous hMSC population. METHODS: Using flow cytometry and cell sorting, we isolated two distinct hMSC-CD146(+) and hMSC-CD146(−) cell populations from the telomerized human bone marrow-derived stromal cell line (hMSC-TERT). Cells were examined for differences in their size, shape and texture by using high-content analysis and additionally for their ability to differentiate toward osteogenesis in vitro and form bone in vivo, and their migrational ability in vivo and in vitro was investigated. RESULTS: In vitro, the two cell populations exhibited similar growth rate and differentiation capacity to osteoblasts and adipocytes on the basis of gene expression and protein production of lineage-specific markers. In vivo, hMSC-CD146(+) and hMSC-CD146(−) cells formed bone and bone marrow organ when implanted subcutaneously in immune-deficient mice. Bone was enriched in hMSC-CD146(−) cells (12.6 % versus 8.1 %) and bone marrow elements enriched in implants containing hMSC-CD146(+) cells (0.5 % versus 0.05 %). hMSC-CD146(+) cells exhibited greater chemotactic attraction in a transwell migration assay and, when injected intravenously into immune-deficient mice following closed femoral fracture, exhibited wider tissue distribution and significantly increased migration ability as demonstrated by bioluminescence imaging. CONCLUSION: Our studies demonstrate that CD146 defines a subpopulation of hMSCs capable of bone formation and in vivo trans-endothelial migration and thus represents a population of hMSCs suitable for use in clinical protocols of bone tissue regeneration. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13287-015-0266-z) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4710006 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-47100062016-01-13 CD146/MCAM defines functionality of human bone marrow stromal stem cell populations Harkness, Linda Zaher, Walid Ditzel, Nicholas Isa, Adiba Kassem, Moustapha Stem Cell Res Ther Research BACKGROUND: Identification of surface markers for prospective isolation of functionally homogenous populations of human skeletal (stromal, mesenchymal) stem cells (hMSCs) is highly relevant for cell therapy protocols. Thus, we examined the possible use of CD146 to subtype a heterogeneous hMSC population. METHODS: Using flow cytometry and cell sorting, we isolated two distinct hMSC-CD146(+) and hMSC-CD146(−) cell populations from the telomerized human bone marrow-derived stromal cell line (hMSC-TERT). Cells were examined for differences in their size, shape and texture by using high-content analysis and additionally for their ability to differentiate toward osteogenesis in vitro and form bone in vivo, and their migrational ability in vivo and in vitro was investigated. RESULTS: In vitro, the two cell populations exhibited similar growth rate and differentiation capacity to osteoblasts and adipocytes on the basis of gene expression and protein production of lineage-specific markers. In vivo, hMSC-CD146(+) and hMSC-CD146(−) cells formed bone and bone marrow organ when implanted subcutaneously in immune-deficient mice. Bone was enriched in hMSC-CD146(−) cells (12.6 % versus 8.1 %) and bone marrow elements enriched in implants containing hMSC-CD146(+) cells (0.5 % versus 0.05 %). hMSC-CD146(+) cells exhibited greater chemotactic attraction in a transwell migration assay and, when injected intravenously into immune-deficient mice following closed femoral fracture, exhibited wider tissue distribution and significantly increased migration ability as demonstrated by bioluminescence imaging. CONCLUSION: Our studies demonstrate that CD146 defines a subpopulation of hMSCs capable of bone formation and in vivo trans-endothelial migration and thus represents a population of hMSCs suitable for use in clinical protocols of bone tissue regeneration. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13287-015-0266-z) contains supplementary material, which is available to authorized users. BioMed Central 2016-01-11 /pmc/articles/PMC4710006/ /pubmed/26753846 http://dx.doi.org/10.1186/s13287-015-0266-z Text en © Harkness et al. 2016 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 | Research Harkness, Linda Zaher, Walid Ditzel, Nicholas Isa, Adiba Kassem, Moustapha CD146/MCAM defines functionality of human bone marrow stromal stem cell populations |
title | CD146/MCAM defines functionality of human bone marrow stromal stem cell populations |
title_full | CD146/MCAM defines functionality of human bone marrow stromal stem cell populations |
title_fullStr | CD146/MCAM defines functionality of human bone marrow stromal stem cell populations |
title_full_unstemmed | CD146/MCAM defines functionality of human bone marrow stromal stem cell populations |
title_short | CD146/MCAM defines functionality of human bone marrow stromal stem cell populations |
title_sort | cd146/mcam defines functionality of human bone marrow stromal stem cell populations |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4710006/ https://www.ncbi.nlm.nih.gov/pubmed/26753846 http://dx.doi.org/10.1186/s13287-015-0266-z |
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