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Drosophila wing imaginal discs respond to mechanical injury via slow InsP(3)R-mediated intercellular calcium waves
Calcium signalling is a highly versatile cellular communication system that modulates basic functions such as cell contractility, essential steps of animal development such as fertilization and higher-order processes such as memory. We probed the function of calcium signalling in Drosophila wing ima...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4980486/ https://www.ncbi.nlm.nih.gov/pubmed/27503836 http://dx.doi.org/10.1038/ncomms12450 |
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author | Restrepo, Simon Basler, Konrad |
author_facet | Restrepo, Simon Basler, Konrad |
author_sort | Restrepo, Simon |
collection | PubMed |
description | Calcium signalling is a highly versatile cellular communication system that modulates basic functions such as cell contractility, essential steps of animal development such as fertilization and higher-order processes such as memory. We probed the function of calcium signalling in Drosophila wing imaginal discs through a combination of ex vivo and in vivo imaging and genetic analysis. Here we discover that wing discs display slow, long-range intercellular calcium waves (ICWs) when mechanically stressed in vivo or cultured ex vivo. These slow imaginal disc intercellular calcium waves (SIDICs) are mediated by the inositol-3-phosphate receptor, the endoplasmic reticulum (ER) calcium pump SERCA and the key gap junction component Inx2. The knockdown of genes required for SIDIC formation and propagation negatively affects wing disc recovery after mechanical injury. Our results reveal a role for ICWs in wing disc homoeostasis and highlight the utility of the wing disc as a model for calcium signalling studies. |
format | Online Article Text |
id | pubmed-4980486 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49804862016-08-12 Drosophila wing imaginal discs respond to mechanical injury via slow InsP(3)R-mediated intercellular calcium waves Restrepo, Simon Basler, Konrad Nat Commun Article Calcium signalling is a highly versatile cellular communication system that modulates basic functions such as cell contractility, essential steps of animal development such as fertilization and higher-order processes such as memory. We probed the function of calcium signalling in Drosophila wing imaginal discs through a combination of ex vivo and in vivo imaging and genetic analysis. Here we discover that wing discs display slow, long-range intercellular calcium waves (ICWs) when mechanically stressed in vivo or cultured ex vivo. These slow imaginal disc intercellular calcium waves (SIDICs) are mediated by the inositol-3-phosphate receptor, the endoplasmic reticulum (ER) calcium pump SERCA and the key gap junction component Inx2. The knockdown of genes required for SIDIC formation and propagation negatively affects wing disc recovery after mechanical injury. Our results reveal a role for ICWs in wing disc homoeostasis and highlight the utility of the wing disc as a model for calcium signalling studies. Nature Publishing Group 2016-08-09 /pmc/articles/PMC4980486/ /pubmed/27503836 http://dx.doi.org/10.1038/ncomms12450 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 Restrepo, Simon Basler, Konrad Drosophila wing imaginal discs respond to mechanical injury via slow InsP(3)R-mediated intercellular calcium waves |
title | Drosophila wing imaginal discs respond to mechanical injury via slow InsP(3)R-mediated intercellular calcium waves |
title_full | Drosophila wing imaginal discs respond to mechanical injury via slow InsP(3)R-mediated intercellular calcium waves |
title_fullStr | Drosophila wing imaginal discs respond to mechanical injury via slow InsP(3)R-mediated intercellular calcium waves |
title_full_unstemmed | Drosophila wing imaginal discs respond to mechanical injury via slow InsP(3)R-mediated intercellular calcium waves |
title_short | Drosophila wing imaginal discs respond to mechanical injury via slow InsP(3)R-mediated intercellular calcium waves |
title_sort | drosophila wing imaginal discs respond to mechanical injury via slow insp(3)r-mediated intercellular calcium waves |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4980486/ https://www.ncbi.nlm.nih.gov/pubmed/27503836 http://dx.doi.org/10.1038/ncomms12450 |
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