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      Cell cycle dynamics of mouse embryonic stem cells in the ground state and during transition to formative pluripotency

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          Abstract

          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.

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          Characterization of Strange Attractors

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            Naive and primed pluripotent states.

            After maternal predetermination gives way to zygotic regulation, a ground state is established within the mammalian embryo. This tabula rasa for embryogenesis is present only transiently in the preimplantation epiblast. Here, we consider how unrestricted cells are first generated and then prepared for lineage commitment. We propose that two phases of pluripotency can be defined: naive and primed. This distinction extends to pluripotent stem cells derived from embryos or by molecular reprogramming ex vivo.
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              Reconstitution of the mouse germ cell specification pathway in culture by pluripotent stem cells.

              The generation of properly functioning gametes in vitro requires reconstitution of the multistepped pathway of germ cell development. We demonstrate here the generation of primordial germ cell-like cells (PGCLCs) in mice with robust capacity for spermatogenesis. PGCLCs were generated from embryonic stem cells (ESCs) and induced pluripotent stem cells (iPSCs) through epiblast-like cells (EpiLCs), a cellular state highly similar to pregastrulating epiblasts but distinct from epiblast stem cells (EpiSCs). Reflecting epiblast development, EpiLC induction from ESCs/iPSCs is a progressive process, and EpiLCs highly competent for the PGC fate are a transient entity. The global transcription profiles, epigenetic reprogramming, and cellular dynamics during PGCLC induction from EpiLCs meticulously capture those associated with PGC specification from the epiblasts. Furthermore, we identify Integrin-β3 and SSEA1 as markers that allow the isolation of PGCLCs with spermatogenic capacity from tumorigenic undifferentiated cells. Our findings provide a paradigm for the first step of in vitro gametogenesis. Copyright © 2011 Elsevier Inc. All rights reserved.
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                Author and article information

                Contributors
                algub@qb.fcen.uba.ar
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                29 May 2019
                29 May 2019
                2019
                : 9
                : 8051
                Affiliations
                [1 ]ISNI 0000 0001 0056 1981, GRID grid.7345.5, Universidad de Buenos Aires, Facultad de Ciencias Exactas y Naturales, Departamento de Química Biológica, Instituto de Química Biológica (IQUIBICEN), Laboratorio de Regulación Génica en Células Madre, ; Buenos Aires, Argentina
                [2 ]ISNI 0000 0004 0620 9892, GRID grid.418954.5, CONICET - Fundación para la Lucha contra las Enfermedades Neurológicas de la Infancia (FLENI), Laboratorio de Investigación de Aplicación a Neurociencias (LIAN), ; Buenos Aires, Argentina
                [3 ]ISNI 0000 0001 0056 1981, GRID grid.7345.5, CONICET - Universidad de Buenos Aires, Instituto de Fisiología, Biología Molecular y Neurociencias (IFIBYNE), ; Buenos Aires, Argentina
                [4 ]ISNI 0000 0001 0056 1981, GRID grid.7345.5, Universidad de Buenos Aires, ; Buenos Aires, Argentina
                [5 ]ISNI 0000 0001 0056 1981, GRID grid.7345.5, Universidad de Buenos Aires, Facultad de Ciencias Exactas y Naturales, Departamento de Fisiología y Biología Molecular y Celular, Buenos Aires, ; Buenos Aires, Argentina
                Author information
                http://orcid.org/0000-0002-6860-9512
                http://orcid.org/0000-0001-6749-4162
                http://orcid.org/0000-0003-0047-4620
                http://orcid.org/0000-0003-2402-3920
                http://orcid.org/0000-0002-5275-3827
                http://orcid.org/0000-0002-4291-6741
                Article
                44537
                10.1038/s41598-019-44537-0
                6541595
                31142785
                ce59e249-e496-416a-8dda-68f2936504bb
                © 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/.

                History
                : 27 October 2018
                : 14 May 2019
                Funding
                Funded by: FundRef https://doi.org/10.13039/501100002923, Consejo Nacional de Investigaciones Científicas y Técnicas (National Scientific and Technical Research Council);
                Award ID: PIP 112-2011010024
                Award Recipient :
                Categories
                Article
                Custom metadata
                © The Author(s) 2019

                Uncategorized
                cellular imaging,data mining,cell growth,embryonic stem cells,self-renewal
                Uncategorized
                cellular imaging, data mining, cell growth, embryonic stem cells, self-renewal

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