Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Martinez, Yannick, Béna, Frédérique, Gimelli, Stefania, Tirefort, Diderik, Dubois-Dauphin, Michel, Krause, Karl-Heinz, Preynat-Seauve, Olivier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2012
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
_version_ 1782290477101350912
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
work_keys_str_mv AT martinezyannick cellulardiversitywithinembryonicstemcellspluripotentclonalsublinesshowdistinctdifferentiationpotential
AT benafrederique cellulardiversitywithinembryonicstemcellspluripotentclonalsublinesshowdistinctdifferentiationpotential
AT gimellistefania cellulardiversitywithinembryonicstemcellspluripotentclonalsublinesshowdistinctdifferentiationpotential
AT tirefortdiderik cellulardiversitywithinembryonicstemcellspluripotentclonalsublinesshowdistinctdifferentiationpotential
AT duboisdauphinmichel cellulardiversitywithinembryonicstemcellspluripotentclonalsublinesshowdistinctdifferentiationpotential
AT krausekarlheinz cellulardiversitywithinembryonicstemcellspluripotentclonalsublinesshowdistinctdifferentiationpotential
AT preynatseauveolivier cellulardiversitywithinembryonicstemcellspluripotentclonalsublinesshowdistinctdifferentiationpotential