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Retinoic acid signaling is critical during the totipotency window in early mammalian development

Totipotent cells hold enormous potential for regenerative medicine. Thus, the development of cellular models recapitulating totipotent-like features is of paramount importance. Cells resembling the totipotent cells of early embryos arise spontaneously in mouse embryonic stem (ES) cell cultures. Such...

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Autores principales: Iturbide, Ane, Ruiz Tejada Segura, Mayra L., Noll, Camille, Schorpp, Kenji, Rothenaigner, Ina, Ruiz-Morales, Elias R., Lubatti, Gabriele, Agami, Ahmed, Hadian, Kamyar, Scialdone, Antonio, Torres-Padilla, Maria-Elena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8195742/
https://www.ncbi.nlm.nih.gov/pubmed/34045724
http://dx.doi.org/10.1038/s41594-021-00590-w
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author Iturbide, Ane
Ruiz Tejada Segura, Mayra L.
Noll, Camille
Schorpp, Kenji
Rothenaigner, Ina
Ruiz-Morales, Elias R.
Lubatti, Gabriele
Agami, Ahmed
Hadian, Kamyar
Scialdone, Antonio
Torres-Padilla, Maria-Elena
author_facet Iturbide, Ane
Ruiz Tejada Segura, Mayra L.
Noll, Camille
Schorpp, Kenji
Rothenaigner, Ina
Ruiz-Morales, Elias R.
Lubatti, Gabriele
Agami, Ahmed
Hadian, Kamyar
Scialdone, Antonio
Torres-Padilla, Maria-Elena
author_sort Iturbide, Ane
collection PubMed
description Totipotent cells hold enormous potential for regenerative medicine. Thus, the development of cellular models recapitulating totipotent-like features is of paramount importance. Cells resembling the totipotent cells of early embryos arise spontaneously in mouse embryonic stem (ES) cell cultures. Such ‘2-cell-like-cells’ (2CLCs) recapitulate 2-cell-stage features and display expanded cell potential. Here, we used 2CLCs to perform a small-molecule screen to identify new pathways regulating the 2-cell-stage program. We identified retinoids as robust inducers of 2CLCs and the retinoic acid (RA)-signaling pathway as a key component of the regulatory circuitry of totipotent cells in embryos. Using single-cell RNA-seq, we reveal the transcriptional dynamics of 2CLC reprogramming and show that ES cells undergo distinct cellular trajectories in response to RA. Importantly, endogenous RA activity in early embryos is essential for zygotic genome activation and developmental progression. Overall, our data shed light on the gene regulatory networks controlling cellular plasticity and the totipotency program.
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spelling pubmed-81957422021-06-28 Retinoic acid signaling is critical during the totipotency window in early mammalian development Iturbide, Ane Ruiz Tejada Segura, Mayra L. Noll, Camille Schorpp, Kenji Rothenaigner, Ina Ruiz-Morales, Elias R. Lubatti, Gabriele Agami, Ahmed Hadian, Kamyar Scialdone, Antonio Torres-Padilla, Maria-Elena Nat Struct Mol Biol Resource Totipotent cells hold enormous potential for regenerative medicine. Thus, the development of cellular models recapitulating totipotent-like features is of paramount importance. Cells resembling the totipotent cells of early embryos arise spontaneously in mouse embryonic stem (ES) cell cultures. Such ‘2-cell-like-cells’ (2CLCs) recapitulate 2-cell-stage features and display expanded cell potential. Here, we used 2CLCs to perform a small-molecule screen to identify new pathways regulating the 2-cell-stage program. We identified retinoids as robust inducers of 2CLCs and the retinoic acid (RA)-signaling pathway as a key component of the regulatory circuitry of totipotent cells in embryos. Using single-cell RNA-seq, we reveal the transcriptional dynamics of 2CLC reprogramming and show that ES cells undergo distinct cellular trajectories in response to RA. Importantly, endogenous RA activity in early embryos is essential for zygotic genome activation and developmental progression. Overall, our data shed light on the gene regulatory networks controlling cellular plasticity and the totipotency program. Nature Publishing Group US 2021-05-27 2021 /pmc/articles/PMC8195742/ /pubmed/34045724 http://dx.doi.org/10.1038/s41594-021-00590-w Text en © The Author(s) 2021, corrected publication 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Resource
Iturbide, Ane
Ruiz Tejada Segura, Mayra L.
Noll, Camille
Schorpp, Kenji
Rothenaigner, Ina
Ruiz-Morales, Elias R.
Lubatti, Gabriele
Agami, Ahmed
Hadian, Kamyar
Scialdone, Antonio
Torres-Padilla, Maria-Elena
Retinoic acid signaling is critical during the totipotency window in early mammalian development
title Retinoic acid signaling is critical during the totipotency window in early mammalian development
title_full Retinoic acid signaling is critical during the totipotency window in early mammalian development
title_fullStr Retinoic acid signaling is critical during the totipotency window in early mammalian development
title_full_unstemmed Retinoic acid signaling is critical during the totipotency window in early mammalian development
title_short Retinoic acid signaling is critical during the totipotency window in early mammalian development
title_sort retinoic acid signaling is critical during the totipotency window in early mammalian development
topic Resource
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8195742/
https://www.ncbi.nlm.nih.gov/pubmed/34045724
http://dx.doi.org/10.1038/s41594-021-00590-w
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