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Rapid nanomolding of nanotopography on flexible substrates to control muscle cell growth with enhanced maturation

In vivo, multiple biophysical cues provided by highly ordered connective tissues of the extracellular matrix regulate skeletal muscle cells to align in parallel with one another. However, in routine in vitro cell culture environments, these key factors are often missing, which leads to changes in ce...

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Autores principales: Wu, Cong, Chin, Chriss S. M., Huang, Qingyun, Chan, Ho-Yin, Yu, Xinge, Roy, Vellaisamy A. L., Li, Wen J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8571286/
https://www.ncbi.nlm.nih.gov/pubmed/34754504
http://dx.doi.org/10.1038/s41378-021-00316-4
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author Wu, Cong
Chin, Chriss S. M.
Huang, Qingyun
Chan, Ho-Yin
Yu, Xinge
Roy, Vellaisamy A. L.
Li, Wen J.
author_facet Wu, Cong
Chin, Chriss S. M.
Huang, Qingyun
Chan, Ho-Yin
Yu, Xinge
Roy, Vellaisamy A. L.
Li, Wen J.
author_sort Wu, Cong
collection PubMed
description In vivo, multiple biophysical cues provided by highly ordered connective tissues of the extracellular matrix regulate skeletal muscle cells to align in parallel with one another. However, in routine in vitro cell culture environments, these key factors are often missing, which leads to changes in cell behavior. Here, we present a simple strategy for using optical media discs with nanogrooves and other polymer-based substrates nanomolded from the discs to directly culture muscle cells to study their response to the effect of biophysical cues such as nanotopography and substrate stiffness. We extend the range of study of biophysical cues for myoblasts by showing that they can sense ripple sizes as small as a 100 nm width and a 20 nm depth for myotube alignment, which has not been reported previously. The results revealed that nanotopography and substrate stiffness regulated myoblast proliferation and morphology independently, with nanotopographical cues showing a higher effect. These biophysical cues also worked synergistically, and their individual effects on cells were additive; i.e., by comparing cells grown on different polymer-based substrates (with and without nanogrooves), the cell proliferation rate could be reduced by as much as ~29%, and the elongation rate could be increased as much as ~116%. Moreover, during myogenesis, muscle cells actively responded to nanotopography and consistently showed increases in fusion and maturation indices of ~28% and ~21%, respectively. Finally, under electrical stimulation, the contraction amplitude of well-aligned myotubes was found to be almost 3 times greater than that for the cells on a smooth surface, regardless of the substrate stiffness.
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spelling pubmed-85712862021-11-08 Rapid nanomolding of nanotopography on flexible substrates to control muscle cell growth with enhanced maturation Wu, Cong Chin, Chriss S. M. Huang, Qingyun Chan, Ho-Yin Yu, Xinge Roy, Vellaisamy A. L. Li, Wen J. Microsyst Nanoeng Article In vivo, multiple biophysical cues provided by highly ordered connective tissues of the extracellular matrix regulate skeletal muscle cells to align in parallel with one another. However, in routine in vitro cell culture environments, these key factors are often missing, which leads to changes in cell behavior. Here, we present a simple strategy for using optical media discs with nanogrooves and other polymer-based substrates nanomolded from the discs to directly culture muscle cells to study their response to the effect of biophysical cues such as nanotopography and substrate stiffness. We extend the range of study of biophysical cues for myoblasts by showing that they can sense ripple sizes as small as a 100 nm width and a 20 nm depth for myotube alignment, which has not been reported previously. The results revealed that nanotopography and substrate stiffness regulated myoblast proliferation and morphology independently, with nanotopographical cues showing a higher effect. These biophysical cues also worked synergistically, and their individual effects on cells were additive; i.e., by comparing cells grown on different polymer-based substrates (with and without nanogrooves), the cell proliferation rate could be reduced by as much as ~29%, and the elongation rate could be increased as much as ~116%. Moreover, during myogenesis, muscle cells actively responded to nanotopography and consistently showed increases in fusion and maturation indices of ~28% and ~21%, respectively. Finally, under electrical stimulation, the contraction amplitude of well-aligned myotubes was found to be almost 3 times greater than that for the cells on a smooth surface, regardless of the substrate stiffness. Nature Publishing Group UK 2021-11-05 /pmc/articles/PMC8571286/ /pubmed/34754504 http://dx.doi.org/10.1038/s41378-021-00316-4 Text en © The Author(s) 2021 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Wu, Cong
Chin, Chriss S. M.
Huang, Qingyun
Chan, Ho-Yin
Yu, Xinge
Roy, Vellaisamy A. L.
Li, Wen J.
Rapid nanomolding of nanotopography on flexible substrates to control muscle cell growth with enhanced maturation
title Rapid nanomolding of nanotopography on flexible substrates to control muscle cell growth with enhanced maturation
title_full Rapid nanomolding of nanotopography on flexible substrates to control muscle cell growth with enhanced maturation
title_fullStr Rapid nanomolding of nanotopography on flexible substrates to control muscle cell growth with enhanced maturation
title_full_unstemmed Rapid nanomolding of nanotopography on flexible substrates to control muscle cell growth with enhanced maturation
title_short Rapid nanomolding of nanotopography on flexible substrates to control muscle cell growth with enhanced maturation
title_sort rapid nanomolding of nanotopography on flexible substrates to control muscle cell growth with enhanced maturation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8571286/
https://www.ncbi.nlm.nih.gov/pubmed/34754504
http://dx.doi.org/10.1038/s41378-021-00316-4
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