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Intercellular Calcium Signaling Induced by ATP Potentiates Macrophage Phagocytosis
Extracellular ATP is a signaling molecule exploited by the immune cells for both autocrine regulation and paracrine communication. By performing live calcium imaging experiments, we show that triggered mouse macrophages are able to propagate calcium signals to resting bystander cells by releasing AT...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6449513/ https://www.ncbi.nlm.nih.gov/pubmed/30943393 http://dx.doi.org/10.1016/j.celrep.2019.03.011 |
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author | Zumerle, Sara Calì, Bianca Munari, Fabio Angioni, Roberta Di Virgilio, Francesco Molon, Barbara Viola, Antonella |
author_facet | Zumerle, Sara Calì, Bianca Munari, Fabio Angioni, Roberta Di Virgilio, Francesco Molon, Barbara Viola, Antonella |
author_sort | Zumerle, Sara |
collection | PubMed |
description | Extracellular ATP is a signaling molecule exploited by the immune cells for both autocrine regulation and paracrine communication. By performing live calcium imaging experiments, we show that triggered mouse macrophages are able to propagate calcium signals to resting bystander cells by releasing ATP. ATP-based intercellular communication is mediated by P2X4 and P2X7 receptors and is a feature of pro-inflammatory macrophages. In terms of functional significance, ATP signaling is required for efficient phagocytosis of pathogen-derived molecules and apoptotic cells and may represent a target for macrophage regulation by CD39-expressing cells. These results highlight a cell-to-cell communication mechanism tuning innate immunity. |
format | Online Article Text |
id | pubmed-6449513 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-64495132019-04-15 Intercellular Calcium Signaling Induced by ATP Potentiates Macrophage Phagocytosis Zumerle, Sara Calì, Bianca Munari, Fabio Angioni, Roberta Di Virgilio, Francesco Molon, Barbara Viola, Antonella Cell Rep Article Extracellular ATP is a signaling molecule exploited by the immune cells for both autocrine regulation and paracrine communication. By performing live calcium imaging experiments, we show that triggered mouse macrophages are able to propagate calcium signals to resting bystander cells by releasing ATP. ATP-based intercellular communication is mediated by P2X4 and P2X7 receptors and is a feature of pro-inflammatory macrophages. In terms of functional significance, ATP signaling is required for efficient phagocytosis of pathogen-derived molecules and apoptotic cells and may represent a target for macrophage regulation by CD39-expressing cells. These results highlight a cell-to-cell communication mechanism tuning innate immunity. Cell Press 2019-04-02 /pmc/articles/PMC6449513/ /pubmed/30943393 http://dx.doi.org/10.1016/j.celrep.2019.03.011 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Zumerle, Sara Calì, Bianca Munari, Fabio Angioni, Roberta Di Virgilio, Francesco Molon, Barbara Viola, Antonella Intercellular Calcium Signaling Induced by ATP Potentiates Macrophage Phagocytosis |
title | Intercellular Calcium Signaling Induced by ATP Potentiates Macrophage Phagocytosis |
title_full | Intercellular Calcium Signaling Induced by ATP Potentiates Macrophage Phagocytosis |
title_fullStr | Intercellular Calcium Signaling Induced by ATP Potentiates Macrophage Phagocytosis |
title_full_unstemmed | Intercellular Calcium Signaling Induced by ATP Potentiates Macrophage Phagocytosis |
title_short | Intercellular Calcium Signaling Induced by ATP Potentiates Macrophage Phagocytosis |
title_sort | intercellular calcium signaling induced by atp potentiates macrophage phagocytosis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6449513/ https://www.ncbi.nlm.nih.gov/pubmed/30943393 http://dx.doi.org/10.1016/j.celrep.2019.03.011 |
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