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Ultra-Soft PDMS-Based Magnetoactive Elastomers as Dynamic Cell Culture Substrata
Mechanical cues such as extracellular matrix stiffness and movement have a major impact on cell differentiation and function. To replicate these biological features in vitro, soft substrata with tunable elasticity and the possibility for controlled surface translocation are desirable. Here we report...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3799858/ https://www.ncbi.nlm.nih.gov/pubmed/24204603 http://dx.doi.org/10.1371/journal.pone.0076196 |
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author | Mayer, Matthias Rabindranath, Raman Börner, Juliane Hörner, Eva Bentz, Alexander Salgado, Josefina Han, Hong Böse, Holger Probst, Jörn Shamonin, Mikhail Monkman, Gareth J. Schlunck, Günther |
author_facet | Mayer, Matthias Rabindranath, Raman Börner, Juliane Hörner, Eva Bentz, Alexander Salgado, Josefina Han, Hong Böse, Holger Probst, Jörn Shamonin, Mikhail Monkman, Gareth J. Schlunck, Günther |
author_sort | Mayer, Matthias |
collection | PubMed |
description | Mechanical cues such as extracellular matrix stiffness and movement have a major impact on cell differentiation and function. To replicate these biological features in vitro, soft substrata with tunable elasticity and the possibility for controlled surface translocation are desirable. Here we report on the use of ultra-soft (Young’s modulus <100 kPa) PDMS-based magnetoactive elastomers (MAE) as suitable cell culture substrata. Soft non-viscous PDMS (<18 kPa) is produced using a modified extended crosslinker. MAEs are generated by embedding magnetic microparticles into a soft PDMS matrix. Both substrata yield an elasticity-dependent (14 vs. 100 kPa) modulation of α-smooth muscle actin expression in primary human fibroblasts. To allow for static or dynamic control of MAE material properties, we devise low magnetic field (≈40 mT) stimulation systems compatible with cell-culture environments. Magnetic field-instigated stiffening (14 to 200 kPa) of soft MAE enhances the spreading of primary human fibroblasts and decreases PAX-7 transcription in human mesenchymal stem cells. Pulsatile MAE movements are generated using oscillating magnetic fields and are well tolerated by adherent human fibroblasts. This MAE system provides spatial and temporal control of substratum material characteristics and permits novel designs when used as dynamic cell culture substrata or cell culture-coated actuator in tissue engineering applications or biomedical devices. |
format | Online Article Text |
id | pubmed-3799858 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-37998582013-11-07 Ultra-Soft PDMS-Based Magnetoactive Elastomers as Dynamic Cell Culture Substrata Mayer, Matthias Rabindranath, Raman Börner, Juliane Hörner, Eva Bentz, Alexander Salgado, Josefina Han, Hong Böse, Holger Probst, Jörn Shamonin, Mikhail Monkman, Gareth J. Schlunck, Günther PLoS One Research Article Mechanical cues such as extracellular matrix stiffness and movement have a major impact on cell differentiation and function. To replicate these biological features in vitro, soft substrata with tunable elasticity and the possibility for controlled surface translocation are desirable. Here we report on the use of ultra-soft (Young’s modulus <100 kPa) PDMS-based magnetoactive elastomers (MAE) as suitable cell culture substrata. Soft non-viscous PDMS (<18 kPa) is produced using a modified extended crosslinker. MAEs are generated by embedding magnetic microparticles into a soft PDMS matrix. Both substrata yield an elasticity-dependent (14 vs. 100 kPa) modulation of α-smooth muscle actin expression in primary human fibroblasts. To allow for static or dynamic control of MAE material properties, we devise low magnetic field (≈40 mT) stimulation systems compatible with cell-culture environments. Magnetic field-instigated stiffening (14 to 200 kPa) of soft MAE enhances the spreading of primary human fibroblasts and decreases PAX-7 transcription in human mesenchymal stem cells. Pulsatile MAE movements are generated using oscillating magnetic fields and are well tolerated by adherent human fibroblasts. This MAE system provides spatial and temporal control of substratum material characteristics and permits novel designs when used as dynamic cell culture substrata or cell culture-coated actuator in tissue engineering applications or biomedical devices. Public Library of Science 2013-10-18 /pmc/articles/PMC3799858/ /pubmed/24204603 http://dx.doi.org/10.1371/journal.pone.0076196 Text en © 2013 Mayer et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Mayer, Matthias Rabindranath, Raman Börner, Juliane Hörner, Eva Bentz, Alexander Salgado, Josefina Han, Hong Böse, Holger Probst, Jörn Shamonin, Mikhail Monkman, Gareth J. Schlunck, Günther Ultra-Soft PDMS-Based Magnetoactive Elastomers as Dynamic Cell Culture Substrata |
title | Ultra-Soft PDMS-Based Magnetoactive Elastomers as Dynamic Cell Culture Substrata |
title_full | Ultra-Soft PDMS-Based Magnetoactive Elastomers as Dynamic Cell Culture Substrata |
title_fullStr | Ultra-Soft PDMS-Based Magnetoactive Elastomers as Dynamic Cell Culture Substrata |
title_full_unstemmed | Ultra-Soft PDMS-Based Magnetoactive Elastomers as Dynamic Cell Culture Substrata |
title_short | Ultra-Soft PDMS-Based Magnetoactive Elastomers as Dynamic Cell Culture Substrata |
title_sort | ultra-soft pdms-based magnetoactive elastomers as dynamic cell culture substrata |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3799858/ https://www.ncbi.nlm.nih.gov/pubmed/24204603 http://dx.doi.org/10.1371/journal.pone.0076196 |
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