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Lysyl oxidase-like 4 involvement in retinoic acid epithelial wound healing

Vitamin A and its active forms (retinoic acids/RAs) are known to have pro-healing properties, but their mechanisms of action are still poorly understood. This work aimed to identify the cellular and molecular processes by which atRA (all-trans RA) improves wound healing, using an in vivo model of mo...

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Autores principales: Comptour, Aurélie, Rouzaire, Marion, Belville, Corinne, Bonnin, Nicolas, Daniel, Estelle, Chiambaretta, Frédéric, Blanchon, Loïc, Sapin, Vincent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5011693/
https://www.ncbi.nlm.nih.gov/pubmed/27597564
http://dx.doi.org/10.1038/srep32688
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author Comptour, Aurélie
Rouzaire, Marion
Belville, Corinne
Bonnin, Nicolas
Daniel, Estelle
Chiambaretta, Frédéric
Blanchon, Loïc
Sapin, Vincent
author_facet Comptour, Aurélie
Rouzaire, Marion
Belville, Corinne
Bonnin, Nicolas
Daniel, Estelle
Chiambaretta, Frédéric
Blanchon, Loïc
Sapin, Vincent
author_sort Comptour, Aurélie
collection PubMed
description Vitamin A and its active forms (retinoic acids/RAs) are known to have pro-healing properties, but their mechanisms of action are still poorly understood. This work aimed to identify the cellular and molecular processes by which atRA (all-trans RA) improves wound healing, using an in vivo model of mouse corneal alkali burns and an in vitro cellular human corneal epithelial injury model. Regulation by atRA has been studied on most of the cellular events that occur in wound healing. We investigated the direct influence of atRA on a specific target gene known to be involved in the extracellular matrix (ECM) dynamics, one of the pathways contributing to epithelial repair. Our results demonstrate that atRA promotes corneal epithelial wound healing by acting preferentially on migration. The induction of lysyl oxidase-like 4 (LOXL4) expression by atRA in the corneal epithelium environment was established as essential in the mechanism of atRA-dependent wound healing. Our study describes for the first time a direct link between a retinoic-induced gene and protein, LOXL4, and its general clinical pro-healing properties in ECM dynamics.
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spelling pubmed-50116932016-09-12 Lysyl oxidase-like 4 involvement in retinoic acid epithelial wound healing Comptour, Aurélie Rouzaire, Marion Belville, Corinne Bonnin, Nicolas Daniel, Estelle Chiambaretta, Frédéric Blanchon, Loïc Sapin, Vincent Sci Rep Article Vitamin A and its active forms (retinoic acids/RAs) are known to have pro-healing properties, but their mechanisms of action are still poorly understood. This work aimed to identify the cellular and molecular processes by which atRA (all-trans RA) improves wound healing, using an in vivo model of mouse corneal alkali burns and an in vitro cellular human corneal epithelial injury model. Regulation by atRA has been studied on most of the cellular events that occur in wound healing. We investigated the direct influence of atRA on a specific target gene known to be involved in the extracellular matrix (ECM) dynamics, one of the pathways contributing to epithelial repair. Our results demonstrate that atRA promotes corneal epithelial wound healing by acting preferentially on migration. The induction of lysyl oxidase-like 4 (LOXL4) expression by atRA in the corneal epithelium environment was established as essential in the mechanism of atRA-dependent wound healing. Our study describes for the first time a direct link between a retinoic-induced gene and protein, LOXL4, and its general clinical pro-healing properties in ECM dynamics. Nature Publishing Group 2016-09-06 /pmc/articles/PMC5011693/ /pubmed/27597564 http://dx.doi.org/10.1038/srep32688 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Comptour, Aurélie
Rouzaire, Marion
Belville, Corinne
Bonnin, Nicolas
Daniel, Estelle
Chiambaretta, Frédéric
Blanchon, Loïc
Sapin, Vincent
Lysyl oxidase-like 4 involvement in retinoic acid epithelial wound healing
title Lysyl oxidase-like 4 involvement in retinoic acid epithelial wound healing
title_full Lysyl oxidase-like 4 involvement in retinoic acid epithelial wound healing
title_fullStr Lysyl oxidase-like 4 involvement in retinoic acid epithelial wound healing
title_full_unstemmed Lysyl oxidase-like 4 involvement in retinoic acid epithelial wound healing
title_short Lysyl oxidase-like 4 involvement in retinoic acid epithelial wound healing
title_sort lysyl oxidase-like 4 involvement in retinoic acid epithelial wound healing
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5011693/
https://www.ncbi.nlm.nih.gov/pubmed/27597564
http://dx.doi.org/10.1038/srep32688
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