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Human induced mesenchymal stem cells display increased sensitivity to matrix stiffness

The clinical translation of mesenchymal stem cells (MSCs) is limited by population heterogeneity and inconsistent responses to engineered signals. Specifically, the extent in which MSCs respond to mechanical cues varies significantly across MSC lines. Although induced pluripotent stem cells (iPSCs)...

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Autores principales: Gultian, Kirstene A., Gandhi, Roshni, Sarin, Khushi, Sladkova-Faure, Martina, Zimmer, Matthew, de Peppo, Giuseppe Maria, Vega, Sebastián L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9119934/
https://www.ncbi.nlm.nih.gov/pubmed/35589731
http://dx.doi.org/10.1038/s41598-022-12143-2
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author Gultian, Kirstene A.
Gandhi, Roshni
Sarin, Khushi
Sladkova-Faure, Martina
Zimmer, Matthew
de Peppo, Giuseppe Maria
Vega, Sebastián L.
author_facet Gultian, Kirstene A.
Gandhi, Roshni
Sarin, Khushi
Sladkova-Faure, Martina
Zimmer, Matthew
de Peppo, Giuseppe Maria
Vega, Sebastián L.
author_sort Gultian, Kirstene A.
collection PubMed
description The clinical translation of mesenchymal stem cells (MSCs) is limited by population heterogeneity and inconsistent responses to engineered signals. Specifically, the extent in which MSCs respond to mechanical cues varies significantly across MSC lines. Although induced pluripotent stem cells (iPSCs) have recently emerged as a novel cell source for creating highly homogeneous MSC (iMSC) lines, cellular mechanosensing of iMSCs on engineered materials with defined mechanics is not well understood. Here, we tested the mechanosensing properties of three human iMSC lines derived from iPSCs generated using a fully automated platform. Stiffness-driven changes in morphology were comparable between MSCs and iMSCs cultured atop hydrogels of different stiffness. However, contrary to tissue derived MSCs, no significant changes in iMSC morphology were observed between iMSC lines atop different stiffness hydrogels, demonstrating a consistent response to mechanical signals. Further, stiffness-driven changes in mechanosensitive biomarkers were more pronounced in iMSCs than MSCs, which shows that iMSCs are more adaptive and responsive to mechanical cues than MSCs. This study reports that iMSCs are a promising stem cell source for basic and applied research due to their homogeneity and high sensitivity to engineered mechanical signals.
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spelling pubmed-91199342022-05-21 Human induced mesenchymal stem cells display increased sensitivity to matrix stiffness Gultian, Kirstene A. Gandhi, Roshni Sarin, Khushi Sladkova-Faure, Martina Zimmer, Matthew de Peppo, Giuseppe Maria Vega, Sebastián L. Sci Rep Article The clinical translation of mesenchymal stem cells (MSCs) is limited by population heterogeneity and inconsistent responses to engineered signals. Specifically, the extent in which MSCs respond to mechanical cues varies significantly across MSC lines. Although induced pluripotent stem cells (iPSCs) have recently emerged as a novel cell source for creating highly homogeneous MSC (iMSC) lines, cellular mechanosensing of iMSCs on engineered materials with defined mechanics is not well understood. Here, we tested the mechanosensing properties of three human iMSC lines derived from iPSCs generated using a fully automated platform. Stiffness-driven changes in morphology were comparable between MSCs and iMSCs cultured atop hydrogels of different stiffness. However, contrary to tissue derived MSCs, no significant changes in iMSC morphology were observed between iMSC lines atop different stiffness hydrogels, demonstrating a consistent response to mechanical signals. Further, stiffness-driven changes in mechanosensitive biomarkers were more pronounced in iMSCs than MSCs, which shows that iMSCs are more adaptive and responsive to mechanical cues than MSCs. This study reports that iMSCs are a promising stem cell source for basic and applied research due to their homogeneity and high sensitivity to engineered mechanical signals. Nature Publishing Group UK 2022-05-19 /pmc/articles/PMC9119934/ /pubmed/35589731 http://dx.doi.org/10.1038/s41598-022-12143-2 Text en © The Author(s) 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Gultian, Kirstene A.
Gandhi, Roshni
Sarin, Khushi
Sladkova-Faure, Martina
Zimmer, Matthew
de Peppo, Giuseppe Maria
Vega, Sebastián L.
Human induced mesenchymal stem cells display increased sensitivity to matrix stiffness
title Human induced mesenchymal stem cells display increased sensitivity to matrix stiffness
title_full Human induced mesenchymal stem cells display increased sensitivity to matrix stiffness
title_fullStr Human induced mesenchymal stem cells display increased sensitivity to matrix stiffness
title_full_unstemmed Human induced mesenchymal stem cells display increased sensitivity to matrix stiffness
title_short Human induced mesenchymal stem cells display increased sensitivity to matrix stiffness
title_sort human induced mesenchymal stem cells display increased sensitivity to matrix stiffness
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9119934/
https://www.ncbi.nlm.nih.gov/pubmed/35589731
http://dx.doi.org/10.1038/s41598-022-12143-2
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