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Sustained Ca(2+) mobilizations: A quantitative approach to predict their importance in cell-cell communication and wound healing
Epithelial wound healing requires the coordination of cells to migrate as a unit over the basement membrane after injury. To understand the process of this coordinated movement, it is critical to study the dynamics of cell-cell communication. We developed a method to characterize the injury-induced...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6481807/ https://www.ncbi.nlm.nih.gov/pubmed/31017899 http://dx.doi.org/10.1371/journal.pone.0213422 |
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author | Lee, Yoonjoo Kim, Min Tae Rhodes, Garrett Sack, Kelsey Son, Sung Jun Rich, Celeste B. Kolachalama, Vijaya B. Gabel, Christopher V. Trinkaus-Randall, Vickery |
author_facet | Lee, Yoonjoo Kim, Min Tae Rhodes, Garrett Sack, Kelsey Son, Sung Jun Rich, Celeste B. Kolachalama, Vijaya B. Gabel, Christopher V. Trinkaus-Randall, Vickery |
author_sort | Lee, Yoonjoo |
collection | PubMed |
description | Epithelial wound healing requires the coordination of cells to migrate as a unit over the basement membrane after injury. To understand the process of this coordinated movement, it is critical to study the dynamics of cell-cell communication. We developed a method to characterize the injury-induced sustained Ca(2+) mobilizations that travel between cells for periods of time up to several hours. These events of communication are concentrated along the wound edge and are reduced in cells further away from the wound. Our goal was to delineate the role and contribution of these sustained mobilizations and using MATLAB analyses, we determined the probability of cell-cell communication events in both in vitro models and ex vivo organ culture models. We demonstrated that the injury response was complex and represented the activation of a number of receptors. In addition, we found that pannexin channels mediated the cell-cell communication and motility. Furthermore, the sustained Ca(2+) mobilizations are associated with changes in cell morphology and motility during wound healing. The results demonstrate that both purinoreceptors and pannexins regulate the sustained Ca(2+) mobilization necessary for cell-cell communication in wound healing. |
format | Online Article Text |
id | pubmed-6481807 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-64818072019-05-07 Sustained Ca(2+) mobilizations: A quantitative approach to predict their importance in cell-cell communication and wound healing Lee, Yoonjoo Kim, Min Tae Rhodes, Garrett Sack, Kelsey Son, Sung Jun Rich, Celeste B. Kolachalama, Vijaya B. Gabel, Christopher V. Trinkaus-Randall, Vickery PLoS One Research Article Epithelial wound healing requires the coordination of cells to migrate as a unit over the basement membrane after injury. To understand the process of this coordinated movement, it is critical to study the dynamics of cell-cell communication. We developed a method to characterize the injury-induced sustained Ca(2+) mobilizations that travel between cells for periods of time up to several hours. These events of communication are concentrated along the wound edge and are reduced in cells further away from the wound. Our goal was to delineate the role and contribution of these sustained mobilizations and using MATLAB analyses, we determined the probability of cell-cell communication events in both in vitro models and ex vivo organ culture models. We demonstrated that the injury response was complex and represented the activation of a number of receptors. In addition, we found that pannexin channels mediated the cell-cell communication and motility. Furthermore, the sustained Ca(2+) mobilizations are associated with changes in cell morphology and motility during wound healing. The results demonstrate that both purinoreceptors and pannexins regulate the sustained Ca(2+) mobilization necessary for cell-cell communication in wound healing. Public Library of Science 2019-04-24 /pmc/articles/PMC6481807/ /pubmed/31017899 http://dx.doi.org/10.1371/journal.pone.0213422 Text en © 2019 Lee et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Lee, Yoonjoo Kim, Min Tae Rhodes, Garrett Sack, Kelsey Son, Sung Jun Rich, Celeste B. Kolachalama, Vijaya B. Gabel, Christopher V. Trinkaus-Randall, Vickery Sustained Ca(2+) mobilizations: A quantitative approach to predict their importance in cell-cell communication and wound healing |
title | Sustained Ca(2+) mobilizations: A quantitative approach to predict their importance in cell-cell communication and wound healing |
title_full | Sustained Ca(2+) mobilizations: A quantitative approach to predict their importance in cell-cell communication and wound healing |
title_fullStr | Sustained Ca(2+) mobilizations: A quantitative approach to predict their importance in cell-cell communication and wound healing |
title_full_unstemmed | Sustained Ca(2+) mobilizations: A quantitative approach to predict their importance in cell-cell communication and wound healing |
title_short | Sustained Ca(2+) mobilizations: A quantitative approach to predict their importance in cell-cell communication and wound healing |
title_sort | sustained ca(2+) mobilizations: a quantitative approach to predict their importance in cell-cell communication and wound healing |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6481807/ https://www.ncbi.nlm.nih.gov/pubmed/31017899 http://dx.doi.org/10.1371/journal.pone.0213422 |
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