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Assessment of corneal substrate biomechanics and its effect on epithelial stem cell maintenance and differentiation

Whilst demonstrated extensively in vitro, the control of cell behaviour via modulation of substrate compliance in live tissues has not been accomplished to date. Here we propose that stem cells can be regulated solely through in situ modulation of tissue biomechanics. By first establishing, via high...

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Autores principales: Gouveia, Ricardo M., Lepert, Guillaume, Gupta, Suneel, Mohan, Rajiv R., Paterson, Carl, Connon, Che J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6447573/
https://www.ncbi.nlm.nih.gov/pubmed/30944320
http://dx.doi.org/10.1038/s41467-019-09331-6
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author Gouveia, Ricardo M.
Lepert, Guillaume
Gupta, Suneel
Mohan, Rajiv R.
Paterson, Carl
Connon, Che J.
author_facet Gouveia, Ricardo M.
Lepert, Guillaume
Gupta, Suneel
Mohan, Rajiv R.
Paterson, Carl
Connon, Che J.
author_sort Gouveia, Ricardo M.
collection PubMed
description Whilst demonstrated extensively in vitro, the control of cell behaviour via modulation of substrate compliance in live tissues has not been accomplished to date. Here we propose that stem cells can be regulated solely through in situ modulation of tissue biomechanics. By first establishing, via high-resolution Brillouin spectro-microscopy, that the outer edge (limbus) of live human corneas has a substantially lower bulk modulus compared to their centre, we then demonstrate that this difference is associated with limbal epithelial stem cell (LESC) residence and YAP-dependent mechanotransduction. This phenotype-through-biomechanics correlation is further explored in vivo using a rabbit alkali burn model. Specifically, we show that treating the burnt surface of the cornea with collagenase effectively restores the tissue’s mechanical properties and its capacity to support LESCs through mechanisms involving YAP suppression. Overall, these findings have extended implications for understanding stem cell niche biomechanics and its impact on tissue regeneration.
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spelling pubmed-64475732019-04-05 Assessment of corneal substrate biomechanics and its effect on epithelial stem cell maintenance and differentiation Gouveia, Ricardo M. Lepert, Guillaume Gupta, Suneel Mohan, Rajiv R. Paterson, Carl Connon, Che J. Nat Commun Article Whilst demonstrated extensively in vitro, the control of cell behaviour via modulation of substrate compliance in live tissues has not been accomplished to date. Here we propose that stem cells can be regulated solely through in situ modulation of tissue biomechanics. By first establishing, via high-resolution Brillouin spectro-microscopy, that the outer edge (limbus) of live human corneas has a substantially lower bulk modulus compared to their centre, we then demonstrate that this difference is associated with limbal epithelial stem cell (LESC) residence and YAP-dependent mechanotransduction. This phenotype-through-biomechanics correlation is further explored in vivo using a rabbit alkali burn model. Specifically, we show that treating the burnt surface of the cornea with collagenase effectively restores the tissue’s mechanical properties and its capacity to support LESCs through mechanisms involving YAP suppression. Overall, these findings have extended implications for understanding stem cell niche biomechanics and its impact on tissue regeneration. Nature Publishing Group UK 2019-04-03 /pmc/articles/PMC6447573/ /pubmed/30944320 http://dx.doi.org/10.1038/s41467-019-09331-6 Text en © The Author(s) 2019 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/.
spellingShingle Article
Gouveia, Ricardo M.
Lepert, Guillaume
Gupta, Suneel
Mohan, Rajiv R.
Paterson, Carl
Connon, Che J.
Assessment of corneal substrate biomechanics and its effect on epithelial stem cell maintenance and differentiation
title Assessment of corneal substrate biomechanics and its effect on epithelial stem cell maintenance and differentiation
title_full Assessment of corneal substrate biomechanics and its effect on epithelial stem cell maintenance and differentiation
title_fullStr Assessment of corneal substrate biomechanics and its effect on epithelial stem cell maintenance and differentiation
title_full_unstemmed Assessment of corneal substrate biomechanics and its effect on epithelial stem cell maintenance and differentiation
title_short Assessment of corneal substrate biomechanics and its effect on epithelial stem cell maintenance and differentiation
title_sort assessment of corneal substrate biomechanics and its effect on epithelial stem cell maintenance and differentiation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6447573/
https://www.ncbi.nlm.nih.gov/pubmed/30944320
http://dx.doi.org/10.1038/s41467-019-09331-6
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