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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...

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Detalles Bibliográficos
Autores principales: Restrepo, Simon, Basler, Konrad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
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.
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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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