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Human Pluripotent Stem Cell Fate Regulation by SMARCB1

Epigenetic regulation by the SWI/SNF complex is essential for normal self-renewal capacity and pluripotency of human pluripotent stem cells (hPSCs). It has been shown that different subunits of the complex have a distinct role in this regulation. Specifically, the SMARCB1 subunit has been shown to r...

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Autores principales: Carmel-Gross, Ilana, Levy, Etgar, Armon, Leah, Yaron, Orly, Waldman Ben-Asher, Hiba, Urbach, Achia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7664050/
https://www.ncbi.nlm.nih.gov/pubmed/33125876
http://dx.doi.org/10.1016/j.stemcr.2020.10.002
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author Carmel-Gross, Ilana
Levy, Etgar
Armon, Leah
Yaron, Orly
Waldman Ben-Asher, Hiba
Urbach, Achia
author_facet Carmel-Gross, Ilana
Levy, Etgar
Armon, Leah
Yaron, Orly
Waldman Ben-Asher, Hiba
Urbach, Achia
author_sort Carmel-Gross, Ilana
collection PubMed
description Epigenetic regulation by the SWI/SNF complex is essential for normal self-renewal capacity and pluripotency of human pluripotent stem cells (hPSCs). It has been shown that different subunits of the complex have a distinct role in this regulation. Specifically, the SMARCB1 subunit has been shown to regulate the activity of enhancers in diverse types of cells, including hPSCs. Here, we report the establishment of conditional hPSC lines, enabling control of SMARCB1 expression from complete loss of function to significant overexpression. Using this system, we show that any deviation from normal SMARCB1 expression leads to cell differentiation. We further found that SMARCB1 expression is not required for differentiation of hPSCs into progenitor cells, but rather for later stages of differentiation. Finally, we identify SMARCB1 as a critical player in regulation of cell-cell and cell-ECM interactions in hPSCs and show that this regulation is mediated at least in part by the WNT pathway.
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spelling pubmed-76640502020-11-20 Human Pluripotent Stem Cell Fate Regulation by SMARCB1 Carmel-Gross, Ilana Levy, Etgar Armon, Leah Yaron, Orly Waldman Ben-Asher, Hiba Urbach, Achia Stem Cell Reports Report Epigenetic regulation by the SWI/SNF complex is essential for normal self-renewal capacity and pluripotency of human pluripotent stem cells (hPSCs). It has been shown that different subunits of the complex have a distinct role in this regulation. Specifically, the SMARCB1 subunit has been shown to regulate the activity of enhancers in diverse types of cells, including hPSCs. Here, we report the establishment of conditional hPSC lines, enabling control of SMARCB1 expression from complete loss of function to significant overexpression. Using this system, we show that any deviation from normal SMARCB1 expression leads to cell differentiation. We further found that SMARCB1 expression is not required for differentiation of hPSCs into progenitor cells, but rather for later stages of differentiation. Finally, we identify SMARCB1 as a critical player in regulation of cell-cell and cell-ECM interactions in hPSCs and show that this regulation is mediated at least in part by the WNT pathway. Elsevier 2020-10-29 /pmc/articles/PMC7664050/ /pubmed/33125876 http://dx.doi.org/10.1016/j.stemcr.2020.10.002 Text en © 2020 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Report
Carmel-Gross, Ilana
Levy, Etgar
Armon, Leah
Yaron, Orly
Waldman Ben-Asher, Hiba
Urbach, Achia
Human Pluripotent Stem Cell Fate Regulation by SMARCB1
title Human Pluripotent Stem Cell Fate Regulation by SMARCB1
title_full Human Pluripotent Stem Cell Fate Regulation by SMARCB1
title_fullStr Human Pluripotent Stem Cell Fate Regulation by SMARCB1
title_full_unstemmed Human Pluripotent Stem Cell Fate Regulation by SMARCB1
title_short Human Pluripotent Stem Cell Fate Regulation by SMARCB1
title_sort human pluripotent stem cell fate regulation by smarcb1
topic Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7664050/
https://www.ncbi.nlm.nih.gov/pubmed/33125876
http://dx.doi.org/10.1016/j.stemcr.2020.10.002
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