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Transcriptomic analysis reveals dynamic molecular changes in skin induced by mechanical forces secondary to tissue expansion

Tissue expansion procedures (TE) utilize mechanical forces to induce skin growth and regeneration. While the impact of quick mechanical stimulation on molecular changes in cells has been studied extensively, there is a clear gap in knowledge about sequential biological processes activated during lon...

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Autores principales: Ledwon, Joanna K., Kelsey, Lauren J., Vaca, Elbert E., Gosain, Arun K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7524724/
https://www.ncbi.nlm.nih.gov/pubmed/32994433
http://dx.doi.org/10.1038/s41598-020-71823-z
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author Ledwon, Joanna K.
Kelsey, Lauren J.
Vaca, Elbert E.
Gosain, Arun K.
author_facet Ledwon, Joanna K.
Kelsey, Lauren J.
Vaca, Elbert E.
Gosain, Arun K.
author_sort Ledwon, Joanna K.
collection PubMed
description Tissue expansion procedures (TE) utilize mechanical forces to induce skin growth and regeneration. While the impact of quick mechanical stimulation on molecular changes in cells has been studied extensively, there is a clear gap in knowledge about sequential biological processes activated during long-term stimulation of skin in vivo. Here, we present the first genome-wide study of transcriptional changes in skin during TE, starting from 1 h to 7 days of expansion. Our results indicate that mechanical forces from a tissue expander induce broad molecular changes in gene expression, and that these changes are time-dependent. We revealed hierarchical changes in skin cell biology, including activation of an immune response, a switch in cell metabolism and processes related to muscle contraction and cytoskeleton organization. In addition to known mechanoresponsive genes (TNC, MMPs), we have identified novel candidate genes (SFRP2, SPP1, CCR1, C2, MSR1, C4A, PLA2G2F, HBB), which might play crucial roles in stretched-induced skin growth. Understanding which biological processes are affected by mechanical forces in TE is important for the development of skin treatments to maximize the efficacy and minimize the risk of complications during expansion procedures.
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spelling pubmed-75247242020-10-01 Transcriptomic analysis reveals dynamic molecular changes in skin induced by mechanical forces secondary to tissue expansion Ledwon, Joanna K. Kelsey, Lauren J. Vaca, Elbert E. Gosain, Arun K. Sci Rep Article Tissue expansion procedures (TE) utilize mechanical forces to induce skin growth and regeneration. While the impact of quick mechanical stimulation on molecular changes in cells has been studied extensively, there is a clear gap in knowledge about sequential biological processes activated during long-term stimulation of skin in vivo. Here, we present the first genome-wide study of transcriptional changes in skin during TE, starting from 1 h to 7 days of expansion. Our results indicate that mechanical forces from a tissue expander induce broad molecular changes in gene expression, and that these changes are time-dependent. We revealed hierarchical changes in skin cell biology, including activation of an immune response, a switch in cell metabolism and processes related to muscle contraction and cytoskeleton organization. In addition to known mechanoresponsive genes (TNC, MMPs), we have identified novel candidate genes (SFRP2, SPP1, CCR1, C2, MSR1, C4A, PLA2G2F, HBB), which might play crucial roles in stretched-induced skin growth. Understanding which biological processes are affected by mechanical forces in TE is important for the development of skin treatments to maximize the efficacy and minimize the risk of complications during expansion procedures. Nature Publishing Group UK 2020-09-29 /pmc/articles/PMC7524724/ /pubmed/32994433 http://dx.doi.org/10.1038/s41598-020-71823-z Text en © The Author(s) 2020, corrected publication 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
Ledwon, Joanna K.
Kelsey, Lauren J.
Vaca, Elbert E.
Gosain, Arun K.
Transcriptomic analysis reveals dynamic molecular changes in skin induced by mechanical forces secondary to tissue expansion
title Transcriptomic analysis reveals dynamic molecular changes in skin induced by mechanical forces secondary to tissue expansion
title_full Transcriptomic analysis reveals dynamic molecular changes in skin induced by mechanical forces secondary to tissue expansion
title_fullStr Transcriptomic analysis reveals dynamic molecular changes in skin induced by mechanical forces secondary to tissue expansion
title_full_unstemmed Transcriptomic analysis reveals dynamic molecular changes in skin induced by mechanical forces secondary to tissue expansion
title_short Transcriptomic analysis reveals dynamic molecular changes in skin induced by mechanical forces secondary to tissue expansion
title_sort transcriptomic analysis reveals dynamic molecular changes in skin induced by mechanical forces secondary to tissue expansion
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7524724/
https://www.ncbi.nlm.nih.gov/pubmed/32994433
http://dx.doi.org/10.1038/s41598-020-71823-z
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