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Cellular diversity within embryonic stem cells: pluripotent clonal sublines show distinct differentiation potential
Embryonic stem cells (ESC), derived from the early inner cell mass (ICM), are constituted of theoretically homogeneous pluripotent cells. Our study was designed to test this concept using experimental approaches that allowed characterization of progenies derived from single parental mouse ESC. Flow...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3822923/ https://www.ncbi.nlm.nih.gov/pubmed/21535399 http://dx.doi.org/10.1111/j.1582-4934.2011.01334.x |
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author | Martinez, Yannick Béna, Frédérique Gimelli, Stefania Tirefort, Diderik Dubois-Dauphin, Michel Krause, Karl-Heinz Preynat-Seauve, Olivier |
author_facet | Martinez, Yannick Béna, Frédérique Gimelli, Stefania Tirefort, Diderik Dubois-Dauphin, Michel Krause, Karl-Heinz Preynat-Seauve, Olivier |
author_sort | Martinez, Yannick |
collection | PubMed |
description | Embryonic stem cells (ESC), derived from the early inner cell mass (ICM), are constituted of theoretically homogeneous pluripotent cells. Our study was designed to test this concept using experimental approaches that allowed characterization of progenies derived from single parental mouse ESC. Flow cytometry analysis showed that a fraction of ESC submitted to neural differentiation generates progenies that escape the desired phenotype. Live imaging of individual cells demonstrated significant variations in the capacity of parental ESC to generate neurons, raising the possibility of clonal diversity among ESC. To further substantiate this hypothesis, clonal sublines from ESC were generated by limit dilution. Transcriptome analysis of undifferentiated sublines showed marked differences in gene expression despite the fact that all clones expressed pluripotency markers. Sublines showed distinct differentiation potential, both in phenotypic differentiation assays and with respect to gene expression in embryoid bodies. Clones generated from another ESC line also showed individualities in their differentiation potential, demonstrating the wider applicability of these findings. Taken together, our observations demonstrate that pluripotent ESC consist of individual cell types with distinct differentiation potentials. These findings identify novel elements for the biological understanding of ESC and provide new tools with a major potential for their future in vitro and in vivo use. |
format | Online Article Text |
id | pubmed-3822923 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-38229232015-03-27 Cellular diversity within embryonic stem cells: pluripotent clonal sublines show distinct differentiation potential Martinez, Yannick Béna, Frédérique Gimelli, Stefania Tirefort, Diderik Dubois-Dauphin, Michel Krause, Karl-Heinz Preynat-Seauve, Olivier J Cell Mol Med Original Articles Embryonic stem cells (ESC), derived from the early inner cell mass (ICM), are constituted of theoretically homogeneous pluripotent cells. Our study was designed to test this concept using experimental approaches that allowed characterization of progenies derived from single parental mouse ESC. Flow cytometry analysis showed that a fraction of ESC submitted to neural differentiation generates progenies that escape the desired phenotype. Live imaging of individual cells demonstrated significant variations in the capacity of parental ESC to generate neurons, raising the possibility of clonal diversity among ESC. To further substantiate this hypothesis, clonal sublines from ESC were generated by limit dilution. Transcriptome analysis of undifferentiated sublines showed marked differences in gene expression despite the fact that all clones expressed pluripotency markers. Sublines showed distinct differentiation potential, both in phenotypic differentiation assays and with respect to gene expression in embryoid bodies. Clones generated from another ESC line also showed individualities in their differentiation potential, demonstrating the wider applicability of these findings. Taken together, our observations demonstrate that pluripotent ESC consist of individual cell types with distinct differentiation potentials. These findings identify novel elements for the biological understanding of ESC and provide new tools with a major potential for their future in vitro and in vivo use. Blackwell Publishing Ltd 2012-03 2012-02-28 /pmc/articles/PMC3822923/ /pubmed/21535399 http://dx.doi.org/10.1111/j.1582-4934.2011.01334.x Text en © 2012 Foundation for Cellular and Molecular Medicine/Blackwell Publishing Ltd |
spellingShingle | Original Articles Martinez, Yannick Béna, Frédérique Gimelli, Stefania Tirefort, Diderik Dubois-Dauphin, Michel Krause, Karl-Heinz Preynat-Seauve, Olivier Cellular diversity within embryonic stem cells: pluripotent clonal sublines show distinct differentiation potential |
title | Cellular diversity within embryonic stem cells: pluripotent clonal sublines show distinct differentiation potential |
title_full | Cellular diversity within embryonic stem cells: pluripotent clonal sublines show distinct differentiation potential |
title_fullStr | Cellular diversity within embryonic stem cells: pluripotent clonal sublines show distinct differentiation potential |
title_full_unstemmed | Cellular diversity within embryonic stem cells: pluripotent clonal sublines show distinct differentiation potential |
title_short | Cellular diversity within embryonic stem cells: pluripotent clonal sublines show distinct differentiation potential |
title_sort | cellular diversity within embryonic stem cells: pluripotent clonal sublines show distinct differentiation potential |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3822923/ https://www.ncbi.nlm.nih.gov/pubmed/21535399 http://dx.doi.org/10.1111/j.1582-4934.2011.01334.x |
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