Tissue homeostasis in the wing disc of Drosophila melanogaster: immediate response to massive damage during development
All organisms have developed mechanisms to respond to organ or tissue damage that may appear during development or during the adult life. This process of regeneration is a major long-standing problem in Developmental Biology. We are using the Drosophila melanogaster wing imaginal disc to study the r...
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description | All organisms have developed mechanisms to respond to organ or tissue damage that may appear during development or during the adult life. This process of regeneration is a major long-standing problem in Developmental Biology. We are using the Drosophila melanogaster wing imaginal disc to study the response to major damage inflicted during development. Using the Gal4/UAS/Gal80(TS) conditional system, we have induced massive cell killing by forcing activity of the pro-apoptotic gene hid in two major regions of the disc as defined by Gal4 inserts in the genes rotund (rn) and spalt (sal). The procedure ensures that at the end of a 40-48 hrs of ablation period the great majority of the cells of the original Rn or Sal domains have been eliminated. The results indicate that the damage provokes an immediate response aimed to keep the integrity of the epithelium and to repair the region under ablation. This includes an increase in cell proliferation to compensate for the cell loss and the replacement of the dead cells by others from outside of the damaged area. The response is almost contemporaneous with the damage, so that at the end of the ablation period the targeted region is already reconstructed. We find that the proliferative response is largely systemic, as the number of cells in division increases all over the disc. Furthermore, our results indicate that the Dpp and Wg pathways are not specifically involved in the regenerative response, but that activity of the JNK pathway is necessary both inside and outside the ablated domain for its reconstruction. |
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This process of regeneration is a major long-standing problem in Developmental Biology. We are using the Drosophila melanogaster wing imaginal disc to study the response to major damage inflicted during development. Using the Gal4/UAS/Gal80(TS) conditional system, we have induced massive cell killing by forcing activity of the pro-apoptotic gene hid in two major regions of the disc as defined by Gal4 inserts in the genes rotund (rn) and spalt (sal). The procedure ensures that at the end of a 40-48 hrs of ablation period the great majority of the cells of the original Rn or Sal domains have been eliminated. The results indicate that the damage provokes an immediate response aimed to keep the integrity of the epithelium and to repair the region under ablation. This includes an increase in cell proliferation to compensate for the cell loss and the replacement of the dead cells by others from outside of the damaged area. The response is almost contemporaneous with the damage, so that at the end of the ablation period the targeted region is already reconstructed. We find that the proliferative response is largely systemic, as the number of cells in division increases all over the disc. Furthermore, our results indicate that the Dpp and Wg pathways are not specifically involved in the regenerative response, but that activity of the JNK pathway is necessary both inside and outside the ablated domain for its reconstruction.</description><identifier>ISSN: 1553-7404</identifier><identifier>ISSN: 1553-7390</identifier><identifier>EISSN: 1553-7404</identifier><identifier>DOI: 10.1371/journal.pgen.1003446</identifier><identifier>PMID: 23633961</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Animal development ; Animals ; Biology ; Cell division ; Cell growth ; Cell Proliferation ; Cellular control mechanisms ; Developmental biology ; Drosophila ; Drosophila melanogaster - genetics ; Drosophila melanogaster - growth & development ; Drosophila melanogaster - metabolism ; Drosophila Proteins - genetics ; Drosophila Proteins - metabolism ; Experiments ; Gene Expression Regulation, Developmental ; Genetic aspects ; Homeodomain Proteins - genetics ; Homeodomain Proteins - metabolism ; Homeostasis ; Imaginal Discs - growth & development ; Imaginal Discs - metabolism ; Insects ; MAP Kinase Signaling System - genetics ; Observations ; Regeneration (Biology) ; Signal Transduction ; Transcription Factors - genetics ; Transcription Factors - metabolism ; Wings, Animal - growth & development ; Wings, Animal - metabolism ; Wnt1 Protein - metabolism</subject><ispartof>PLoS genetics, 2013-04, Vol.9 (4), p.e1003446-e1003446</ispartof><rights>COPYRIGHT 2013 Public Library of Science</rights><rights>2013 Herrera et al 2013 Herrera et al</rights><rights>2013 Herrera et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Herrera SC, Martín R, Morata G (2013) Tissue Homeostasis in the Wing Disc of Drosophila melanogaster: Immediate Response to Massive Damage during Development. 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This process of regeneration is a major long-standing problem in Developmental Biology. We are using the Drosophila melanogaster wing imaginal disc to study the response to major damage inflicted during development. Using the Gal4/UAS/Gal80(TS) conditional system, we have induced massive cell killing by forcing activity of the pro-apoptotic gene hid in two major regions of the disc as defined by Gal4 inserts in the genes rotund (rn) and spalt (sal). The procedure ensures that at the end of a 40-48 hrs of ablation period the great majority of the cells of the original Rn or Sal domains have been eliminated. The results indicate that the damage provokes an immediate response aimed to keep the integrity of the epithelium and to repair the region under ablation. This includes an increase in cell proliferation to compensate for the cell loss and the replacement of the dead cells by others from outside of the damaged area. The response is almost contemporaneous with the damage, so that at the end of the ablation period the targeted region is already reconstructed. We find that the proliferative response is largely systemic, as the number of cells in division increases all over the disc. Furthermore, our results indicate that the Dpp and Wg pathways are not specifically involved in the regenerative response, but that activity of the JNK pathway is necessary both inside and outside the ablated domain for its reconstruction.</description><subject>Animal development</subject><subject>Animals</subject><subject>Biology</subject><subject>Cell division</subject><subject>Cell growth</subject><subject>Cell Proliferation</subject><subject>Cellular control mechanisms</subject><subject>Developmental biology</subject><subject>Drosophila</subject><subject>Drosophila melanogaster - genetics</subject><subject>Drosophila melanogaster - growth & development</subject><subject>Drosophila melanogaster - metabolism</subject><subject>Drosophila Proteins - genetics</subject><subject>Drosophila Proteins - metabolism</subject><subject>Experiments</subject><subject>Gene Expression Regulation, Developmental</subject><subject>Genetic aspects</subject><subject>Homeodomain Proteins - genetics</subject><subject>Homeodomain Proteins - metabolism</subject><subject>Homeostasis</subject><subject>Imaginal Discs - growth & development</subject><subject>Imaginal Discs - metabolism</subject><subject>Insects</subject><subject>MAP Kinase Signaling System - genetics</subject><subject>Observations</subject><subject>Regeneration (Biology)</subject><subject>Signal Transduction</subject><subject>Transcription Factors - genetics</subject><subject>Transcription Factors - metabolism</subject><subject>Wings, Animal - growth & development</subject><subject>Wings, Animal - metabolism</subject><subject>Wnt1 Protein - metabolism</subject><issn>1553-7404</issn><issn>1553-7390</issn><issn>1553-7404</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>DOA</sourceid><recordid>eNqVk12L1DAUhoso7rr6D0QDgujFjEmTJo0XwrJ-DSwu6OptyKSnbZa2qUk6q__ezM7sMgUvlFyckDznzcn5yLKnBC8JFeTNlZv8oLvl2MCwJBhTxvi97JgUBV0Ihtn9g_1R9iiEq8QUpRQPs6OcckolJ8fZ9aUNYQLUuh5ciDrYgOyAYgvo2g4NqmwwyNXovXfBja3tNOqh04NrdIjg3yLb91BZHQF5CKMbAqDoUK9DsBtAle51k8zkb8RgA50bexji4-xBrbsAT_b2JPv-8cPl2efF-cWn1dnp-cJwWcaFrDGnTOa5Ibw0DOPSSFLSitfcyEIXFZHEEBACV4yuWVFyYSgXTNeYMUKBnmTPd7pj54La5ywoQgsiMRE8T8RqR1ROX6nR217738ppq24OnG-U9tGaDpSs67XAVOTpeSYJlhUjVWFqWWpDMOCk9W7_2rROaTHpo153M9H5zWBb1biNSvXgmNIk8Gov4N3PCUJUfSoAdCnj4KZt3EyIssQFSeiLHdroFJodapcUzRZXp5TivCAF3Ua0_AuVVgW9NW6A2qbzmcPrmUNiIvyKjZ5CUKtvX_-D_fLv7MWPOfvygG1Bd7ENrpuiTf01B9kONKk9g4f6LtUEq-2U3FZcbadE7ackuT07LNOd0-1Y0D9GGQxg</recordid><startdate>20130401</startdate><enddate>20130401</enddate><creator>Herrera, Salvador C</creator><creator>Martín, Raquel</creator><creator>Morata, Ginés</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IOV</scope><scope>ISN</scope><scope>ISR</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20130401</creationdate><title>Tissue homeostasis in the wing disc of Drosophila melanogaster: immediate response to massive damage during development</title><author>Herrera, Salvador C ; Martín, Raquel ; Morata, Ginés</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c698t-9f0634922c168c4008c9183d6f6c95a5d191c1e770d43b45867c3674af04413e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Animal development</topic><topic>Animals</topic><topic>Biology</topic><topic>Cell division</topic><topic>Cell growth</topic><topic>Cell Proliferation</topic><topic>Cellular control mechanisms</topic><topic>Developmental biology</topic><topic>Drosophila</topic><topic>Drosophila melanogaster - genetics</topic><topic>Drosophila melanogaster - growth & development</topic><topic>Drosophila melanogaster - metabolism</topic><topic>Drosophila Proteins - genetics</topic><topic>Drosophila Proteins - metabolism</topic><topic>Experiments</topic><topic>Gene Expression Regulation, Developmental</topic><topic>Genetic aspects</topic><topic>Homeodomain Proteins - genetics</topic><topic>Homeodomain Proteins - metabolism</topic><topic>Homeostasis</topic><topic>Imaginal Discs - growth & development</topic><topic>Imaginal Discs - metabolism</topic><topic>Insects</topic><topic>MAP Kinase Signaling System - genetics</topic><topic>Observations</topic><topic>Regeneration (Biology)</topic><topic>Signal Transduction</topic><topic>Transcription Factors - genetics</topic><topic>Transcription Factors - metabolism</topic><topic>Wings, Animal - growth & development</topic><topic>Wings, Animal - metabolism</topic><topic>Wnt1 Protein - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Herrera, Salvador C</creatorcontrib><creatorcontrib>Martín, Raquel</creatorcontrib><creatorcontrib>Morata, Ginés</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Canada</collection><collection>Gale In Context: Science</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PLoS genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Herrera, Salvador C</au><au>Martín, Raquel</au><au>Morata, Ginés</au><au>Perrimon, Norbert</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tissue homeostasis in the wing disc of Drosophila melanogaster: immediate response to massive damage during development</atitle><jtitle>PLoS genetics</jtitle><addtitle>PLoS Genet</addtitle><date>2013-04-01</date><risdate>2013</risdate><volume>9</volume><issue>4</issue><spage>e1003446</spage><epage>e1003446</epage><pages>e1003446-e1003446</pages><issn>1553-7404</issn><issn>1553-7390</issn><eissn>1553-7404</eissn><abstract>All organisms have developed mechanisms to respond to organ or tissue damage that may appear during development or during the adult life. This process of regeneration is a major long-standing problem in Developmental Biology. We are using the Drosophila melanogaster wing imaginal disc to study the response to major damage inflicted during development. Using the Gal4/UAS/Gal80(TS) conditional system, we have induced massive cell killing by forcing activity of the pro-apoptotic gene hid in two major regions of the disc as defined by Gal4 inserts in the genes rotund (rn) and spalt (sal). The procedure ensures that at the end of a 40-48 hrs of ablation period the great majority of the cells of the original Rn or Sal domains have been eliminated. The results indicate that the damage provokes an immediate response aimed to keep the integrity of the epithelium and to repair the region under ablation. This includes an increase in cell proliferation to compensate for the cell loss and the replacement of the dead cells by others from outside of the damaged area. The response is almost contemporaneous with the damage, so that at the end of the ablation period the targeted region is already reconstructed. We find that the proliferative response is largely systemic, as the number of cells in division increases all over the disc. Furthermore, our results indicate that the Dpp and Wg pathways are not specifically involved in the regenerative response, but that activity of the JNK pathway is necessary both inside and outside the ablated domain for its reconstruction.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>23633961</pmid><doi>10.1371/journal.pgen.1003446</doi><oa>free_for_read</oa></addata></record> |
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subjects | Animal development Animals Biology Cell division Cell growth Cell Proliferation Cellular control mechanisms Developmental biology Drosophila Drosophila melanogaster - genetics Drosophila melanogaster - growth & development Drosophila melanogaster - metabolism Drosophila Proteins - genetics Drosophila Proteins - metabolism Experiments Gene Expression Regulation, Developmental Genetic aspects Homeodomain Proteins - genetics Homeodomain Proteins - metabolism Homeostasis Imaginal Discs - growth & development Imaginal Discs - metabolism Insects MAP Kinase Signaling System - genetics Observations Regeneration (Biology) Signal Transduction Transcription Factors - genetics Transcription Factors - metabolism Wings, Animal - growth & development Wings, Animal - metabolism Wnt1 Protein - metabolism |
title | Tissue homeostasis in the wing disc of Drosophila melanogaster: immediate response to massive damage during development |
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