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Blastomeres of 8-cell mouse embryos differ in their ability to generate embryonic stem cells and produce lines with different transcriptional signatures

Embryonic stem cell (ESC) derivation from single blastomeres of 8-cell mouse embryos results in lower derivation rates than that from whole blastocysts, raising a biological question about the developmental potential of sister blastomeres. We aimed to assess the ability of 8-cell blastomeres to prod...

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Autores principales: Alonso-Alonso, Sandra, Esteve-Codina, Anna, Martin-Mur, Beatriz, Álvarez-González, Lucia, Ruiz-Herrera, Aurora, Santaló, Josep, Ibáñez, Elena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10591181/
https://www.ncbi.nlm.nih.gov/pubmed/37876553
http://dx.doi.org/10.3389/fcell.2023.1274660
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author Alonso-Alonso, Sandra
Esteve-Codina, Anna
Martin-Mur, Beatriz
Álvarez-González, Lucia
Ruiz-Herrera, Aurora
Santaló, Josep
Ibáñez, Elena
author_facet Alonso-Alonso, Sandra
Esteve-Codina, Anna
Martin-Mur, Beatriz
Álvarez-González, Lucia
Ruiz-Herrera, Aurora
Santaló, Josep
Ibáñez, Elena
author_sort Alonso-Alonso, Sandra
collection PubMed
description Embryonic stem cell (ESC) derivation from single blastomeres of 8-cell mouse embryos results in lower derivation rates than that from whole blastocysts, raising a biological question about the developmental potential of sister blastomeres. We aimed to assess the ability of 8-cell blastomeres to produce epiblast cells and ESC lines after isolation, and the properties of the resulting lines. Our results revealed unequal competence among sister blastomeres to produce ESC lines. At least half of the blastomeres possess a lower potential to generate ESCs, although culture conditions and blastomeres plasticity can redirect their non-pluripotent fate towards the epiblast lineage, allowing us to generate up to seven lines from the same embryo. Lines originated from the same embryo segregated into two groups according to their transcriptional signatures. While the expression of genes related to pluripotency and development was higher in one group, no differences were found in their trilineage differentiation ability. These results may help to improve our understanding of the ESC derivation process from single blastomeres and cell fate determination in the preimplantation mouse embryos.
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spelling pubmed-105911812023-10-24 Blastomeres of 8-cell mouse embryos differ in their ability to generate embryonic stem cells and produce lines with different transcriptional signatures Alonso-Alonso, Sandra Esteve-Codina, Anna Martin-Mur, Beatriz Álvarez-González, Lucia Ruiz-Herrera, Aurora Santaló, Josep Ibáñez, Elena Front Cell Dev Biol Cell and Developmental Biology Embryonic stem cell (ESC) derivation from single blastomeres of 8-cell mouse embryos results in lower derivation rates than that from whole blastocysts, raising a biological question about the developmental potential of sister blastomeres. We aimed to assess the ability of 8-cell blastomeres to produce epiblast cells and ESC lines after isolation, and the properties of the resulting lines. Our results revealed unequal competence among sister blastomeres to produce ESC lines. At least half of the blastomeres possess a lower potential to generate ESCs, although culture conditions and blastomeres plasticity can redirect their non-pluripotent fate towards the epiblast lineage, allowing us to generate up to seven lines from the same embryo. Lines originated from the same embryo segregated into two groups according to their transcriptional signatures. While the expression of genes related to pluripotency and development was higher in one group, no differences were found in their trilineage differentiation ability. These results may help to improve our understanding of the ESC derivation process from single blastomeres and cell fate determination in the preimplantation mouse embryos. Frontiers Media S.A. 2023-10-09 /pmc/articles/PMC10591181/ /pubmed/37876553 http://dx.doi.org/10.3389/fcell.2023.1274660 Text en Copyright © 2023 Alonso-Alonso, Esteve-Codina, Martin-Mur, Álvarez-González, Ruiz-Herrera, Santaló and Ibáñez. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Alonso-Alonso, Sandra
Esteve-Codina, Anna
Martin-Mur, Beatriz
Álvarez-González, Lucia
Ruiz-Herrera, Aurora
Santaló, Josep
Ibáñez, Elena
Blastomeres of 8-cell mouse embryos differ in their ability to generate embryonic stem cells and produce lines with different transcriptional signatures
title Blastomeres of 8-cell mouse embryos differ in their ability to generate embryonic stem cells and produce lines with different transcriptional signatures
title_full Blastomeres of 8-cell mouse embryos differ in their ability to generate embryonic stem cells and produce lines with different transcriptional signatures
title_fullStr Blastomeres of 8-cell mouse embryos differ in their ability to generate embryonic stem cells and produce lines with different transcriptional signatures
title_full_unstemmed Blastomeres of 8-cell mouse embryos differ in their ability to generate embryonic stem cells and produce lines with different transcriptional signatures
title_short Blastomeres of 8-cell mouse embryos differ in their ability to generate embryonic stem cells and produce lines with different transcriptional signatures
title_sort blastomeres of 8-cell mouse embryos differ in their ability to generate embryonic stem cells and produce lines with different transcriptional signatures
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10591181/
https://www.ncbi.nlm.nih.gov/pubmed/37876553
http://dx.doi.org/10.3389/fcell.2023.1274660
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