Serine proteolytic pathway activation reveals an expanded ensemble of wound response genes in Drosophila.

After injury to the animal epidermis, a variety of genes are transcriptionally activated in nearby cells to regenerate the missing cells and facilitate barrier repair. The range and types of diffusible wound signals that are produced by damaged epidermis and function to activate repair genes during...

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Main Authors: Rachel A Patterson, Michelle T Juarez, Anita Hermann, Roman Sasik, Gary Hardiman, William McGinnis
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3634835?pdf=render
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author Rachel A Patterson
Michelle T Juarez
Anita Hermann
Roman Sasik
Gary Hardiman
William McGinnis
author_facet Rachel A Patterson
Michelle T Juarez
Anita Hermann
Roman Sasik
Gary Hardiman
William McGinnis
author_sort Rachel A Patterson
collection DOAJ
description After injury to the animal epidermis, a variety of genes are transcriptionally activated in nearby cells to regenerate the missing cells and facilitate barrier repair. The range and types of diffusible wound signals that are produced by damaged epidermis and function to activate repair genes during epidermal regeneration remains a subject of very active study in many animals. In Drosophila embryos, we have discovered that serine protease function is locally activated around wound sites, and is also required for localized activation of epidermal repair genes. The serine protease trypsin is sufficient to induce a striking global epidermal wound response without inflicting cell death or compromising the integrity of the epithelial barrier. We developed a trypsin wounding treatment as an amplification tool to more fully understand the changes in the Drosophila transcriptome that occur after epidermal injury. By comparing our array results with similar results on mammalian skin wounding we can see which evolutionarily conserved pathways are activated after epidermal wounding in very diverse animals. Our innovative serine protease-mediated wounding protocol allowed us to identify 8 additional genes that are activated in epidermal cells in the immediate vicinity of puncture wounds, and the functions of many of these genes suggest novel genetic pathways that may control epidermal wound repair. Additionally, our data augments the evidence that clean puncture wounding can mount a powerful innate immune transcriptional response, with different innate immune genes being activated in an interesting variety of ways. These include puncture-induced activation only in epidermal cells in the immediate vicinity of wounds, or in all epidermal cells, or specifically in the fat body, or in multiple tissues.
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spelling doaj.art-125b5599006d415d843bb8952b29a4a32022-12-21T20:32:56ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0184e6177310.1371/journal.pone.0061773Serine proteolytic pathway activation reveals an expanded ensemble of wound response genes in Drosophila.Rachel A PattersonMichelle T JuarezAnita HermannRoman SasikGary HardimanWilliam McGinnisAfter injury to the animal epidermis, a variety of genes are transcriptionally activated in nearby cells to regenerate the missing cells and facilitate barrier repair. The range and types of diffusible wound signals that are produced by damaged epidermis and function to activate repair genes during epidermal regeneration remains a subject of very active study in many animals. In Drosophila embryos, we have discovered that serine protease function is locally activated around wound sites, and is also required for localized activation of epidermal repair genes. The serine protease trypsin is sufficient to induce a striking global epidermal wound response without inflicting cell death or compromising the integrity of the epithelial barrier. We developed a trypsin wounding treatment as an amplification tool to more fully understand the changes in the Drosophila transcriptome that occur after epidermal injury. By comparing our array results with similar results on mammalian skin wounding we can see which evolutionarily conserved pathways are activated after epidermal wounding in very diverse animals. Our innovative serine protease-mediated wounding protocol allowed us to identify 8 additional genes that are activated in epidermal cells in the immediate vicinity of puncture wounds, and the functions of many of these genes suggest novel genetic pathways that may control epidermal wound repair. Additionally, our data augments the evidence that clean puncture wounding can mount a powerful innate immune transcriptional response, with different innate immune genes being activated in an interesting variety of ways. These include puncture-induced activation only in epidermal cells in the immediate vicinity of wounds, or in all epidermal cells, or specifically in the fat body, or in multiple tissues.http://europepmc.org/articles/PMC3634835?pdf=render
spellingShingle Rachel A Patterson
Michelle T Juarez
Anita Hermann
Roman Sasik
Gary Hardiman
William McGinnis
Serine proteolytic pathway activation reveals an expanded ensemble of wound response genes in Drosophila.
PLoS ONE
title Serine proteolytic pathway activation reveals an expanded ensemble of wound response genes in Drosophila.
title_full Serine proteolytic pathway activation reveals an expanded ensemble of wound response genes in Drosophila.
title_fullStr Serine proteolytic pathway activation reveals an expanded ensemble of wound response genes in Drosophila.
title_full_unstemmed Serine proteolytic pathway activation reveals an expanded ensemble of wound response genes in Drosophila.
title_short Serine proteolytic pathway activation reveals an expanded ensemble of wound response genes in Drosophila.
title_sort serine proteolytic pathway activation reveals an expanded ensemble of wound response genes in drosophila
url http://europepmc.org/articles/PMC3634835?pdf=render
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