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GM-CSF perturbs cell identity in mouse pre-implantation embryos

Growth factors became attractive candidates for medium supplementation to further improve the quality of embryo culture and to mimic in vivo nutrition. Granulocyte macrophage colony-stimulating factor (GM-CSF) is a cytokine influencing the maternal-fetal interface and supporting placental developmen...

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Autores principales: Pock, Tim, Schulte, Katharina, Schlatt, Stefan, Boiani, Michele, Nordhoff, Verena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8830693/
https://www.ncbi.nlm.nih.gov/pubmed/35143564
http://dx.doi.org/10.1371/journal.pone.0263793
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author Pock, Tim
Schulte, Katharina
Schlatt, Stefan
Boiani, Michele
Nordhoff, Verena
author_facet Pock, Tim
Schulte, Katharina
Schlatt, Stefan
Boiani, Michele
Nordhoff, Verena
author_sort Pock, Tim
collection PubMed
description Growth factors became attractive candidates for medium supplementation to further improve the quality of embryo culture and to mimic in vivo nutrition. Granulocyte macrophage colony-stimulating factor (GM-CSF) is a cytokine influencing the maternal-fetal interface and supporting placental development in mouse and human. It is expressed in epithelial cells of the endometrium under the regulation of estrogens. The factor is already in clinical use and a large clinical trial showed that, if supplemented to an embryo culture medium, it leads to increased survival of embryos, especially in women with previous miscarriages. Animal and cell culture studies on isolated trophectoderm cells support an effect mainly on cellular expansion. Aim of this study was to investigate, if the supplementation of GM-CSF either in a human ART medium or in a mouse optimized medium, leads to a change in cell number and cell lineages in the early pre-implantation mouse embryo. Our data shows that mouse GM-CSF increased total cell numbers with increasing concentrations. This increase of cell number has not been found in embryos cultured in ART media with or without human GM-CSF (hGM-CSF) or in a mouse medium supplemented with different concentrations of hGM-CSF. The changes were caused by a marked difference in TE and primitive endoderm cell numbers but not due to a change in epiblast cell numbers. Additionally, results show an ectopic expression of NANOG among trophectoderm cells in both, human ART media (with and without GM-CSF) and at increasing concentrations in the mouse and the human GM-CSF supplemented media. In conclusion, we could show that GM-CSF has an effect on cell identity in mice, which might probably also occur in the human. Therefore, we would like to rare awareness that the use of supplements without proper research could bare risks for the embryo itself and probably also in the post-implantation phase.
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spelling pubmed-88306932022-02-11 GM-CSF perturbs cell identity in mouse pre-implantation embryos Pock, Tim Schulte, Katharina Schlatt, Stefan Boiani, Michele Nordhoff, Verena PLoS One Research Article Growth factors became attractive candidates for medium supplementation to further improve the quality of embryo culture and to mimic in vivo nutrition. Granulocyte macrophage colony-stimulating factor (GM-CSF) is a cytokine influencing the maternal-fetal interface and supporting placental development in mouse and human. It is expressed in epithelial cells of the endometrium under the regulation of estrogens. The factor is already in clinical use and a large clinical trial showed that, if supplemented to an embryo culture medium, it leads to increased survival of embryos, especially in women with previous miscarriages. Animal and cell culture studies on isolated trophectoderm cells support an effect mainly on cellular expansion. Aim of this study was to investigate, if the supplementation of GM-CSF either in a human ART medium or in a mouse optimized medium, leads to a change in cell number and cell lineages in the early pre-implantation mouse embryo. Our data shows that mouse GM-CSF increased total cell numbers with increasing concentrations. This increase of cell number has not been found in embryos cultured in ART media with or without human GM-CSF (hGM-CSF) or in a mouse medium supplemented with different concentrations of hGM-CSF. The changes were caused by a marked difference in TE and primitive endoderm cell numbers but not due to a change in epiblast cell numbers. Additionally, results show an ectopic expression of NANOG among trophectoderm cells in both, human ART media (with and without GM-CSF) and at increasing concentrations in the mouse and the human GM-CSF supplemented media. In conclusion, we could show that GM-CSF has an effect on cell identity in mice, which might probably also occur in the human. Therefore, we would like to rare awareness that the use of supplements without proper research could bare risks for the embryo itself and probably also in the post-implantation phase. Public Library of Science 2022-02-10 /pmc/articles/PMC8830693/ /pubmed/35143564 http://dx.doi.org/10.1371/journal.pone.0263793 Text en © 2022 Pock et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Pock, Tim
Schulte, Katharina
Schlatt, Stefan
Boiani, Michele
Nordhoff, Verena
GM-CSF perturbs cell identity in mouse pre-implantation embryos
title GM-CSF perturbs cell identity in mouse pre-implantation embryos
title_full GM-CSF perturbs cell identity in mouse pre-implantation embryos
title_fullStr GM-CSF perturbs cell identity in mouse pre-implantation embryos
title_full_unstemmed GM-CSF perturbs cell identity in mouse pre-implantation embryos
title_short GM-CSF perturbs cell identity in mouse pre-implantation embryos
title_sort gm-csf perturbs cell identity in mouse pre-implantation embryos
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8830693/
https://www.ncbi.nlm.nih.gov/pubmed/35143564
http://dx.doi.org/10.1371/journal.pone.0263793
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