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Establishment of a primed pluripotent epiblast stem cell in FGF4-based conditions
Several mouse pluripotent stem cell types have been established either from mouse blastocysts and epiblasts. Among these, embryonic stem cells (ESCs) are considered to represent a “naïve”, epiblast stem cells (EpiSCs) a “primed” pluripotent state. Although EpiSCs form derivatives of all three germ l...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4268649/ https://www.ncbi.nlm.nih.gov/pubmed/25515008 http://dx.doi.org/10.1038/srep07477 |
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author | Joo, Jin Young Choi, Hyun Woo Kim, Min Jung Zaehres, Holm Tapia, Natalia Stehling, Martin Jung, Koo Sung Tae, Jeong Schöler, Hans R. |
author_facet | Joo, Jin Young Choi, Hyun Woo Kim, Min Jung Zaehres, Holm Tapia, Natalia Stehling, Martin Jung, Koo Sung Tae, Jeong Schöler, Hans R. |
author_sort | Joo, Jin Young |
collection | PubMed |
description | Several mouse pluripotent stem cell types have been established either from mouse blastocysts and epiblasts. Among these, embryonic stem cells (ESCs) are considered to represent a “naïve”, epiblast stem cells (EpiSCs) a “primed” pluripotent state. Although EpiSCs form derivatives of all three germ layers during in vitro differentiation, they rarely incorporate into the inner cell mass of blastocysts and rarely contribute to chimera formation following blastocyst injection. Here we successfully established homogeneous population of EpiSC lines with efficient chimera-forming capability using a medium containing fibroblast growth factor (FGF)-4. The expression levels of Rex1 and Nanog was very low although Oct4 level is comparable to ESCs. EpiSCs also expressed higher levels of epiblast markers, such as Cer1, Eomes, Fgf5, Sox17, and T, and further showed complete DNA methylation of Stella and Dppa5 promoters. However, the EpiSCs were clustered separately from E3 and T9 EpiSC lines and showed a completely different global gene expression pattern to ESCs. Furthermore, the EpiSCs were able to differentiate into all three germ layers in vitro and efficiently formed teratomas and chimeric embryos (21.4%) without germ-line contribution. |
format | Online Article Text |
id | pubmed-4268649 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-42686492014-12-18 Establishment of a primed pluripotent epiblast stem cell in FGF4-based conditions Joo, Jin Young Choi, Hyun Woo Kim, Min Jung Zaehres, Holm Tapia, Natalia Stehling, Martin Jung, Koo Sung Tae, Jeong Schöler, Hans R. Sci Rep Article Several mouse pluripotent stem cell types have been established either from mouse blastocysts and epiblasts. Among these, embryonic stem cells (ESCs) are considered to represent a “naïve”, epiblast stem cells (EpiSCs) a “primed” pluripotent state. Although EpiSCs form derivatives of all three germ layers during in vitro differentiation, they rarely incorporate into the inner cell mass of blastocysts and rarely contribute to chimera formation following blastocyst injection. Here we successfully established homogeneous population of EpiSC lines with efficient chimera-forming capability using a medium containing fibroblast growth factor (FGF)-4. The expression levels of Rex1 and Nanog was very low although Oct4 level is comparable to ESCs. EpiSCs also expressed higher levels of epiblast markers, such as Cer1, Eomes, Fgf5, Sox17, and T, and further showed complete DNA methylation of Stella and Dppa5 promoters. However, the EpiSCs were clustered separately from E3 and T9 EpiSC lines and showed a completely different global gene expression pattern to ESCs. Furthermore, the EpiSCs were able to differentiate into all three germ layers in vitro and efficiently formed teratomas and chimeric embryos (21.4%) without germ-line contribution. Nature Publishing Group 2014-12-17 /pmc/articles/PMC4268649/ /pubmed/25515008 http://dx.doi.org/10.1038/srep07477 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Joo, Jin Young Choi, Hyun Woo Kim, Min Jung Zaehres, Holm Tapia, Natalia Stehling, Martin Jung, Koo Sung Tae, Jeong Schöler, Hans R. Establishment of a primed pluripotent epiblast stem cell in FGF4-based conditions |
title | Establishment of a primed pluripotent epiblast stem cell in FGF4-based conditions |
title_full | Establishment of a primed pluripotent epiblast stem cell in FGF4-based conditions |
title_fullStr | Establishment of a primed pluripotent epiblast stem cell in FGF4-based conditions |
title_full_unstemmed | Establishment of a primed pluripotent epiblast stem cell in FGF4-based conditions |
title_short | Establishment of a primed pluripotent epiblast stem cell in FGF4-based conditions |
title_sort | establishment of a primed pluripotent epiblast stem cell in fgf4-based conditions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4268649/ https://www.ncbi.nlm.nih.gov/pubmed/25515008 http://dx.doi.org/10.1038/srep07477 |
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