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Calcium spikes, waves and oscillations in a large, patterned epithelial tissue
While calcium signaling in excitable cells, such as muscle or neurons, is extensively characterized, calcium signaling in epithelial tissues is little understood. Specifically, the range of intercellular calcium signaling patterns elicited by tightly coupled epithelial cells and their function in th...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5317010/ https://www.ncbi.nlm.nih.gov/pubmed/28218282 http://dx.doi.org/10.1038/srep42786 |
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author | Balaji, Ramya Bielmeier, Christina Harz, Hartmann Bates, Jack Stadler, Cornelia Hildebrand, Alexander Classen, Anne-Kathrin |
author_facet | Balaji, Ramya Bielmeier, Christina Harz, Hartmann Bates, Jack Stadler, Cornelia Hildebrand, Alexander Classen, Anne-Kathrin |
author_sort | Balaji, Ramya |
collection | PubMed |
description | While calcium signaling in excitable cells, such as muscle or neurons, is extensively characterized, calcium signaling in epithelial tissues is little understood. Specifically, the range of intercellular calcium signaling patterns elicited by tightly coupled epithelial cells and their function in the regulation of epithelial characteristics are little explored. We found that in Drosophila imaginal discs, a widely studied epithelial model organ, complex spatiotemporal calcium dynamics occur. We describe patterns that include intercellular waves traversing large tissue domains in striking oscillatory patterns as well as spikes confined to local domains of neighboring cells. The spatiotemporal characteristics of intercellular waves and oscillations arise as emergent properties of calcium mobilization within a sheet of gap-junction coupled cells and are influenced by cell size and environmental history. While the in vivo function of spikes, waves and oscillations requires further characterization, our genetic experiments suggest that core calcium signaling components guide actomyosin organization. Our study thus suggests a possible role for calcium signaling in epithelia but importantly, introduces a model epithelium enabling the dissection of cellular mechanisms supporting the initiation, transmission and regeneration of long-range intercellular calcium waves and the emergence of oscillations in a highly coupled multicellular sheet. |
format | Online Article Text |
id | pubmed-5317010 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53170102017-02-24 Calcium spikes, waves and oscillations in a large, patterned epithelial tissue Balaji, Ramya Bielmeier, Christina Harz, Hartmann Bates, Jack Stadler, Cornelia Hildebrand, Alexander Classen, Anne-Kathrin Sci Rep Article While calcium signaling in excitable cells, such as muscle or neurons, is extensively characterized, calcium signaling in epithelial tissues is little understood. Specifically, the range of intercellular calcium signaling patterns elicited by tightly coupled epithelial cells and their function in the regulation of epithelial characteristics are little explored. We found that in Drosophila imaginal discs, a widely studied epithelial model organ, complex spatiotemporal calcium dynamics occur. We describe patterns that include intercellular waves traversing large tissue domains in striking oscillatory patterns as well as spikes confined to local domains of neighboring cells. The spatiotemporal characteristics of intercellular waves and oscillations arise as emergent properties of calcium mobilization within a sheet of gap-junction coupled cells and are influenced by cell size and environmental history. While the in vivo function of spikes, waves and oscillations requires further characterization, our genetic experiments suggest that core calcium signaling components guide actomyosin organization. Our study thus suggests a possible role for calcium signaling in epithelia but importantly, introduces a model epithelium enabling the dissection of cellular mechanisms supporting the initiation, transmission and regeneration of long-range intercellular calcium waves and the emergence of oscillations in a highly coupled multicellular sheet. Nature Publishing Group 2017-02-20 /pmc/articles/PMC5317010/ /pubmed/28218282 http://dx.doi.org/10.1038/srep42786 Text en Copyright © 2017, 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 Balaji, Ramya Bielmeier, Christina Harz, Hartmann Bates, Jack Stadler, Cornelia Hildebrand, Alexander Classen, Anne-Kathrin Calcium spikes, waves and oscillations in a large, patterned epithelial tissue |
title | Calcium spikes, waves and oscillations in a large, patterned epithelial tissue |
title_full | Calcium spikes, waves and oscillations in a large, patterned epithelial tissue |
title_fullStr | Calcium spikes, waves and oscillations in a large, patterned epithelial tissue |
title_full_unstemmed | Calcium spikes, waves and oscillations in a large, patterned epithelial tissue |
title_short | Calcium spikes, waves and oscillations in a large, patterned epithelial tissue |
title_sort | calcium spikes, waves and oscillations in a large, patterned epithelial tissue |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5317010/ https://www.ncbi.nlm.nih.gov/pubmed/28218282 http://dx.doi.org/10.1038/srep42786 |
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