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Comparison of Differentiation Pattern and WNT/SHH Signaling in Pluripotent Stem Cells Cultured under Different Conditions

Pluripotent stem cells (PSCs) are characterized by the ability to self-renew as well as undergo multidirectional differentiation. Culture conditions have a pivotal influence on differentiation pattern. In the current study, we compared the fate of mouse PSCs using two culture media: (1) chemically d...

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Autores principales: Świerczek-Lasek, Barbara, Dudka, Damian, Bauer, Damian, Czajkowski, Tomasz, Ilach, Katarzyna, Streminska, Władysława, Kominek, Agata, Piwocka, Katarzyna, Ciemerych, Maria A., Archacka, Karolina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8534321/
https://www.ncbi.nlm.nih.gov/pubmed/34685722
http://dx.doi.org/10.3390/cells10102743
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author Świerczek-Lasek, Barbara
Dudka, Damian
Bauer, Damian
Czajkowski, Tomasz
Ilach, Katarzyna
Streminska, Władysława
Kominek, Agata
Piwocka, Katarzyna
Ciemerych, Maria A.
Archacka, Karolina
author_facet Świerczek-Lasek, Barbara
Dudka, Damian
Bauer, Damian
Czajkowski, Tomasz
Ilach, Katarzyna
Streminska, Władysława
Kominek, Agata
Piwocka, Katarzyna
Ciemerych, Maria A.
Archacka, Karolina
author_sort Świerczek-Lasek, Barbara
collection PubMed
description Pluripotent stem cells (PSCs) are characterized by the ability to self-renew as well as undergo multidirectional differentiation. Culture conditions have a pivotal influence on differentiation pattern. In the current study, we compared the fate of mouse PSCs using two culture media: (1) chemically defined, free of animal reagents, and (2) standard one relying on the serum supplementation. Moreover, we assessed the influence of selected regulators (WNTs, SHH) on PSC differentiation. We showed that the differentiation pattern of PSCs cultured in both systems differed significantly: cells cultured in chemically defined medium preferentially underwent ectodermal conversion while their endo- and mesodermal differentiation was limited, contrary to cells cultured in serum-supplemented medium. More efficient ectodermal differentiation of PSCs cultured in chemically defined medium correlated with higher activity of SHH pathway while endodermal and mesodermal conversion of cells cultured in serum-supplemented medium with higher activity of WNT/JNK pathway. However, inhibition of either canonical or noncanonical WNT pathway resulted in the limitation of endo- and mesodermal conversion of PSCs. In addition, blocking WNT secretion led to the inhibition of PSC mesodermal differentiation, confirming the pivotal role of WNT signaling in this process. In contrast, SHH turned out to be an inducer of PSC ectodermal, not mesodermal differentiation.
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spelling pubmed-85343212021-10-23 Comparison of Differentiation Pattern and WNT/SHH Signaling in Pluripotent Stem Cells Cultured under Different Conditions Świerczek-Lasek, Barbara Dudka, Damian Bauer, Damian Czajkowski, Tomasz Ilach, Katarzyna Streminska, Władysława Kominek, Agata Piwocka, Katarzyna Ciemerych, Maria A. Archacka, Karolina Cells Article Pluripotent stem cells (PSCs) are characterized by the ability to self-renew as well as undergo multidirectional differentiation. Culture conditions have a pivotal influence on differentiation pattern. In the current study, we compared the fate of mouse PSCs using two culture media: (1) chemically defined, free of animal reagents, and (2) standard one relying on the serum supplementation. Moreover, we assessed the influence of selected regulators (WNTs, SHH) on PSC differentiation. We showed that the differentiation pattern of PSCs cultured in both systems differed significantly: cells cultured in chemically defined medium preferentially underwent ectodermal conversion while their endo- and mesodermal differentiation was limited, contrary to cells cultured in serum-supplemented medium. More efficient ectodermal differentiation of PSCs cultured in chemically defined medium correlated with higher activity of SHH pathway while endodermal and mesodermal conversion of cells cultured in serum-supplemented medium with higher activity of WNT/JNK pathway. However, inhibition of either canonical or noncanonical WNT pathway resulted in the limitation of endo- and mesodermal conversion of PSCs. In addition, blocking WNT secretion led to the inhibition of PSC mesodermal differentiation, confirming the pivotal role of WNT signaling in this process. In contrast, SHH turned out to be an inducer of PSC ectodermal, not mesodermal differentiation. MDPI 2021-10-14 /pmc/articles/PMC8534321/ /pubmed/34685722 http://dx.doi.org/10.3390/cells10102743 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Świerczek-Lasek, Barbara
Dudka, Damian
Bauer, Damian
Czajkowski, Tomasz
Ilach, Katarzyna
Streminska, Władysława
Kominek, Agata
Piwocka, Katarzyna
Ciemerych, Maria A.
Archacka, Karolina
Comparison of Differentiation Pattern and WNT/SHH Signaling in Pluripotent Stem Cells Cultured under Different Conditions
title Comparison of Differentiation Pattern and WNT/SHH Signaling in Pluripotent Stem Cells Cultured under Different Conditions
title_full Comparison of Differentiation Pattern and WNT/SHH Signaling in Pluripotent Stem Cells Cultured under Different Conditions
title_fullStr Comparison of Differentiation Pattern and WNT/SHH Signaling in Pluripotent Stem Cells Cultured under Different Conditions
title_full_unstemmed Comparison of Differentiation Pattern and WNT/SHH Signaling in Pluripotent Stem Cells Cultured under Different Conditions
title_short Comparison of Differentiation Pattern and WNT/SHH Signaling in Pluripotent Stem Cells Cultured under Different Conditions
title_sort comparison of differentiation pattern and wnt/shh signaling in pluripotent stem cells cultured under different conditions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8534321/
https://www.ncbi.nlm.nih.gov/pubmed/34685722
http://dx.doi.org/10.3390/cells10102743
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