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Cell cycle dynamics of mouse embryonic stem cells in the ground state and during transition to formative pluripotency
Mouse embryonic stem cells (mESCs) can be maintained as homogeneous populations in the ground state of pluripotency. Release from this state in minimal conditions allows to obtain cells that resemble those of the early post-implantation epiblast, providing an important developmental model to study c...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6541595/ https://www.ncbi.nlm.nih.gov/pubmed/31142785 http://dx.doi.org/10.1038/s41598-019-44537-0 |
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author | Waisman, Ariel Sevlever, Federico Elías Costa, Martín Cosentino, María Soledad Miriuka, Santiago G. Ventura, Alejandra C. Guberman, Alejandra S. |
author_facet | Waisman, Ariel Sevlever, Federico Elías Costa, Martín Cosentino, María Soledad Miriuka, Santiago G. Ventura, Alejandra C. Guberman, Alejandra S. |
author_sort | Waisman, Ariel |
collection | PubMed |
description | Mouse embryonic stem cells (mESCs) can be maintained as homogeneous populations in the ground state of pluripotency. Release from this state in minimal conditions allows to obtain cells that resemble those of the early post-implantation epiblast, providing an important developmental model to study cell identity transitions. However, the cell cycle dynamics of mESCs in the ground state and during its dissolution have not been extensively studied. By performing live imaging experiments of mESCs bearing cell cycle reporters, we show here that cells in the pluripotent ground state display a cell cycle structure comparable to the reported for mESCs in serum-based media. Upon release from self-renewal, the cell cycle is rapidly accelerated by a reduction in the length of the G1 phase and of the S/G2/M phases, causing an increased proliferation rate. Analysis of cell lineages indicates that cell cycle variables of sister cells are highly correlated, suggesting the existence of inherited cell cycle regulators from the parental cell. Together with a major morphological reconfiguration upon differentiation, our findings support a correlation between this in vitro model and early embryonic events. |
format | Online Article Text |
id | pubmed-6541595 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-65415952019-06-07 Cell cycle dynamics of mouse embryonic stem cells in the ground state and during transition to formative pluripotency Waisman, Ariel Sevlever, Federico Elías Costa, Martín Cosentino, María Soledad Miriuka, Santiago G. Ventura, Alejandra C. Guberman, Alejandra S. Sci Rep Article Mouse embryonic stem cells (mESCs) can be maintained as homogeneous populations in the ground state of pluripotency. Release from this state in minimal conditions allows to obtain cells that resemble those of the early post-implantation epiblast, providing an important developmental model to study cell identity transitions. However, the cell cycle dynamics of mESCs in the ground state and during its dissolution have not been extensively studied. By performing live imaging experiments of mESCs bearing cell cycle reporters, we show here that cells in the pluripotent ground state display a cell cycle structure comparable to the reported for mESCs in serum-based media. Upon release from self-renewal, the cell cycle is rapidly accelerated by a reduction in the length of the G1 phase and of the S/G2/M phases, causing an increased proliferation rate. Analysis of cell lineages indicates that cell cycle variables of sister cells are highly correlated, suggesting the existence of inherited cell cycle regulators from the parental cell. Together with a major morphological reconfiguration upon differentiation, our findings support a correlation between this in vitro model and early embryonic events. Nature Publishing Group UK 2019-05-29 /pmc/articles/PMC6541595/ /pubmed/31142785 http://dx.doi.org/10.1038/s41598-019-44537-0 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Waisman, Ariel Sevlever, Federico Elías Costa, Martín Cosentino, María Soledad Miriuka, Santiago G. Ventura, Alejandra C. Guberman, Alejandra S. Cell cycle dynamics of mouse embryonic stem cells in the ground state and during transition to formative pluripotency |
title | Cell cycle dynamics of mouse embryonic stem cells in the ground state and during transition to formative pluripotency |
title_full | Cell cycle dynamics of mouse embryonic stem cells in the ground state and during transition to formative pluripotency |
title_fullStr | Cell cycle dynamics of mouse embryonic stem cells in the ground state and during transition to formative pluripotency |
title_full_unstemmed | Cell cycle dynamics of mouse embryonic stem cells in the ground state and during transition to formative pluripotency |
title_short | Cell cycle dynamics of mouse embryonic stem cells in the ground state and during transition to formative pluripotency |
title_sort | cell cycle dynamics of mouse embryonic stem cells in the ground state and during transition to formative pluripotency |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6541595/ https://www.ncbi.nlm.nih.gov/pubmed/31142785 http://dx.doi.org/10.1038/s41598-019-44537-0 |
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