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Distinct inflammatory and wound healing responses to complex caudal fin injuries of larval zebrafish
Wound repair is controlled temporally and spatially to restore tissue homeostasis. Previously we reported that thermal damage of the larval zebrafish fin disrupts collagen organization and wound healing compared to tail transection (LeBert et al., 2018). Here we characterize different injury models...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6602581/ https://www.ncbi.nlm.nih.gov/pubmed/31259685 http://dx.doi.org/10.7554/eLife.45976 |
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author | Miskolci, Veronika Squirrell, Jayne Rindy, Julie Vincent, William Sauer, John Demian Gibson, Angela Eliceiri, Kevin W Huttenlocher, Anna |
author_facet | Miskolci, Veronika Squirrell, Jayne Rindy, Julie Vincent, William Sauer, John Demian Gibson, Angela Eliceiri, Kevin W Huttenlocher, Anna |
author_sort | Miskolci, Veronika |
collection | PubMed |
description | Wound repair is controlled temporally and spatially to restore tissue homeostasis. Previously we reported that thermal damage of the larval zebrafish fin disrupts collagen organization and wound healing compared to tail transection (LeBert et al., 2018). Here we characterize different injury models in larval zebrafish to dissect temporal and spatial dynamics of repair in complex damage. We found that each damage model triggers distinct inflammatory and tissue responses, with Stat3 and TGFβ playing key roles in the regulation of mesenchymal cells during simple repair. While thermal injury disrupts collagen fibers initially, healing is recovered as inflammation resolves, and mesenchymal cells and collagen fibers align. By contrast, infected wounds lead to persistent inflammation and loss of mesenchymal cells, resulting in minimal tissue repair. These wound models have broad physiological relevance, thereby providing a valuable advance in our toolkit to probe the dynamics of inflammation and wound repair in complex tissue damage. |
format | Online Article Text |
id | pubmed-6602581 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-66025812019-07-03 Distinct inflammatory and wound healing responses to complex caudal fin injuries of larval zebrafish Miskolci, Veronika Squirrell, Jayne Rindy, Julie Vincent, William Sauer, John Demian Gibson, Angela Eliceiri, Kevin W Huttenlocher, Anna eLife Cell Biology Wound repair is controlled temporally and spatially to restore tissue homeostasis. Previously we reported that thermal damage of the larval zebrafish fin disrupts collagen organization and wound healing compared to tail transection (LeBert et al., 2018). Here we characterize different injury models in larval zebrafish to dissect temporal and spatial dynamics of repair in complex damage. We found that each damage model triggers distinct inflammatory and tissue responses, with Stat3 and TGFβ playing key roles in the regulation of mesenchymal cells during simple repair. While thermal injury disrupts collagen fibers initially, healing is recovered as inflammation resolves, and mesenchymal cells and collagen fibers align. By contrast, infected wounds lead to persistent inflammation and loss of mesenchymal cells, resulting in minimal tissue repair. These wound models have broad physiological relevance, thereby providing a valuable advance in our toolkit to probe the dynamics of inflammation and wound repair in complex tissue damage. eLife Sciences Publications, Ltd 2019-07-01 /pmc/articles/PMC6602581/ /pubmed/31259685 http://dx.doi.org/10.7554/eLife.45976 Text en © 2019, Miskolci et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Cell Biology Miskolci, Veronika Squirrell, Jayne Rindy, Julie Vincent, William Sauer, John Demian Gibson, Angela Eliceiri, Kevin W Huttenlocher, Anna Distinct inflammatory and wound healing responses to complex caudal fin injuries of larval zebrafish |
title | Distinct inflammatory and wound healing responses to complex caudal fin injuries of larval zebrafish |
title_full | Distinct inflammatory and wound healing responses to complex caudal fin injuries of larval zebrafish |
title_fullStr | Distinct inflammatory and wound healing responses to complex caudal fin injuries of larval zebrafish |
title_full_unstemmed | Distinct inflammatory and wound healing responses to complex caudal fin injuries of larval zebrafish |
title_short | Distinct inflammatory and wound healing responses to complex caudal fin injuries of larval zebrafish |
title_sort | distinct inflammatory and wound healing responses to complex caudal fin injuries of larval zebrafish |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6602581/ https://www.ncbi.nlm.nih.gov/pubmed/31259685 http://dx.doi.org/10.7554/eLife.45976 |
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