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An ES-Like Pluripotent State in FGF-Dependent Murine iPS cells

Recent data demonstrates that stem cells can exist in two morphologically, molecularly and functionally distinct pluripotent states; a naïve LIF-dependent pluripotent state which is represented by murine embryonic stem cells (mESCs) and an FGF-dependent primed pluripotent state represented by murine...

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Autores principales: Di Stefano, Bruno, Buecker, Christa, Ungaro, Federica, Prigione, Alessandro, Chen, Hsu-Hsin, Welling, Maaike, Eijpe, Maureen, Mostoslavsky, Gustavo, Tesar, Paul, Adjaye, James, Geijsen, Niels, Broccoli, Vania
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3012723/
https://www.ncbi.nlm.nih.gov/pubmed/21209851
http://dx.doi.org/10.1371/journal.pone.0016092
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author Di Stefano, Bruno
Buecker, Christa
Ungaro, Federica
Prigione, Alessandro
Chen, Hsu-Hsin
Welling, Maaike
Eijpe, Maureen
Mostoslavsky, Gustavo
Tesar, Paul
Adjaye, James
Geijsen, Niels
Broccoli, Vania
author_facet Di Stefano, Bruno
Buecker, Christa
Ungaro, Federica
Prigione, Alessandro
Chen, Hsu-Hsin
Welling, Maaike
Eijpe, Maureen
Mostoslavsky, Gustavo
Tesar, Paul
Adjaye, James
Geijsen, Niels
Broccoli, Vania
author_sort Di Stefano, Bruno
collection PubMed
description Recent data demonstrates that stem cells can exist in two morphologically, molecularly and functionally distinct pluripotent states; a naïve LIF-dependent pluripotent state which is represented by murine embryonic stem cells (mESCs) and an FGF-dependent primed pluripotent state represented by murine and rat epiblast stem cells (EpiSCs). We find that derivation of induced pluripotent stem cells (iPSCs) under EpiSC culture conditions yields FGF-dependent iPSCs from hereon called FGF-iPSCs) which, unexpectedly, display naïve ES-like/ICM properties. FGF-iPSCs display X-chromosome activation, multi-lineage differentiation, teratoma competence and chimera contribution in vivo. Our findings suggest that in 129 and Bl6 mouse strains, iPSCs can dominantly adopt a naive pluripotent state regardless of culture growth factor conditions. Characterization of the key molecular signalling pathways revealed FGF-iPSCs to depend on the Activin/Nodal and FGF pathways, while signalling through the JAK-STAT pathway is not required for FGF-iPS cell maintenance. Our findings suggest that in 129 and Bl6 mouse strains, iPSCs can dominantly adopt a naive pluripotent state regardless of culture growth factor conditions.
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spelling pubmed-30127232011-01-05 An ES-Like Pluripotent State in FGF-Dependent Murine iPS cells Di Stefano, Bruno Buecker, Christa Ungaro, Federica Prigione, Alessandro Chen, Hsu-Hsin Welling, Maaike Eijpe, Maureen Mostoslavsky, Gustavo Tesar, Paul Adjaye, James Geijsen, Niels Broccoli, Vania PLoS One Research Article Recent data demonstrates that stem cells can exist in two morphologically, molecularly and functionally distinct pluripotent states; a naïve LIF-dependent pluripotent state which is represented by murine embryonic stem cells (mESCs) and an FGF-dependent primed pluripotent state represented by murine and rat epiblast stem cells (EpiSCs). We find that derivation of induced pluripotent stem cells (iPSCs) under EpiSC culture conditions yields FGF-dependent iPSCs from hereon called FGF-iPSCs) which, unexpectedly, display naïve ES-like/ICM properties. FGF-iPSCs display X-chromosome activation, multi-lineage differentiation, teratoma competence and chimera contribution in vivo. Our findings suggest that in 129 and Bl6 mouse strains, iPSCs can dominantly adopt a naive pluripotent state regardless of culture growth factor conditions. Characterization of the key molecular signalling pathways revealed FGF-iPSCs to depend on the Activin/Nodal and FGF pathways, while signalling through the JAK-STAT pathway is not required for FGF-iPS cell maintenance. Our findings suggest that in 129 and Bl6 mouse strains, iPSCs can dominantly adopt a naive pluripotent state regardless of culture growth factor conditions. Public Library of Science 2010-12-30 /pmc/articles/PMC3012723/ /pubmed/21209851 http://dx.doi.org/10.1371/journal.pone.0016092 Text en Di Stefano et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Di Stefano, Bruno
Buecker, Christa
Ungaro, Federica
Prigione, Alessandro
Chen, Hsu-Hsin
Welling, Maaike
Eijpe, Maureen
Mostoslavsky, Gustavo
Tesar, Paul
Adjaye, James
Geijsen, Niels
Broccoli, Vania
An ES-Like Pluripotent State in FGF-Dependent Murine iPS cells
title An ES-Like Pluripotent State in FGF-Dependent Murine iPS cells
title_full An ES-Like Pluripotent State in FGF-Dependent Murine iPS cells
title_fullStr An ES-Like Pluripotent State in FGF-Dependent Murine iPS cells
title_full_unstemmed An ES-Like Pluripotent State in FGF-Dependent Murine iPS cells
title_short An ES-Like Pluripotent State in FGF-Dependent Murine iPS cells
title_sort es-like pluripotent state in fgf-dependent murine ips cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3012723/
https://www.ncbi.nlm.nih.gov/pubmed/21209851
http://dx.doi.org/10.1371/journal.pone.0016092
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