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Transient Cell Membrane Disruptions induce Calcium Waves in Corneal Keratocytes
The purpose of this study was to determine if transient cell membrane disruptions (TPMDs) in single keratocytes can trigger signaling events in neighboring keratocytes. Stromal cells were cultured from human corneas (HCSC) and mouse corneas (MCSC). TPMDs were produced using a multiphoton microscope...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7029045/ https://www.ncbi.nlm.nih.gov/pubmed/32071321 http://dx.doi.org/10.1038/s41598-020-59570-7 |
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author | Chen, Zhong Lu, Xiaowen McGee-Lawrence, Meghan E. Watsky, Mitchell A. |
author_facet | Chen, Zhong Lu, Xiaowen McGee-Lawrence, Meghan E. Watsky, Mitchell A. |
author_sort | Chen, Zhong |
collection | PubMed |
description | The purpose of this study was to determine if transient cell membrane disruptions (TPMDs) in single keratocytes can trigger signaling events in neighboring keratocytes. Stromal cells were cultured from human corneas (HCSC) and mouse corneas (MCSC). TPMDs were produced using a multiphoton microscope in Cal-520-AM loaded cells. TPMD-induced calcium increases (Ca(++)(i)) were measured in Ca(++)-containing and Ca(++)-free solutions containing thapsigargin, ryanodine, BAPTA-AM, 18-α-glycyrrhetinic acid (18α-GA), apyrase, BCTC, AMG 9810, or AMTB. Fluorescence intensity was recorded as the number of cells responding and the area under the fluorescence versus time curve. The maximum distance of responding neighboring cells in ex vivo human corneas was measured. Connexin 43 protein in HCSC and MCSC was examined using immunofluorescence staining, and corneal rubbing was applied to confirm whether TPMDs occur following mechanical manipulation. Our results demonstrate that single cell TPMDs result in Ca(++) waves in neighboring keratocytes both in culture and within ex vivo corneas. The source of Ca(++) is both intra-and extra-cellular, and the signal can be mediated by ATP and/or gap junctions, and is species dependent. Stromal rubbing confirmed that TPMDs do occur following mechanical manipulation. Keratocyte TPMDs and their associated signaling events are likely common occurrences following minor or major corneal trauma. |
format | Online Article Text |
id | pubmed-7029045 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70290452020-02-26 Transient Cell Membrane Disruptions induce Calcium Waves in Corneal Keratocytes Chen, Zhong Lu, Xiaowen McGee-Lawrence, Meghan E. Watsky, Mitchell A. Sci Rep Article The purpose of this study was to determine if transient cell membrane disruptions (TPMDs) in single keratocytes can trigger signaling events in neighboring keratocytes. Stromal cells were cultured from human corneas (HCSC) and mouse corneas (MCSC). TPMDs were produced using a multiphoton microscope in Cal-520-AM loaded cells. TPMD-induced calcium increases (Ca(++)(i)) were measured in Ca(++)-containing and Ca(++)-free solutions containing thapsigargin, ryanodine, BAPTA-AM, 18-α-glycyrrhetinic acid (18α-GA), apyrase, BCTC, AMG 9810, or AMTB. Fluorescence intensity was recorded as the number of cells responding and the area under the fluorescence versus time curve. The maximum distance of responding neighboring cells in ex vivo human corneas was measured. Connexin 43 protein in HCSC and MCSC was examined using immunofluorescence staining, and corneal rubbing was applied to confirm whether TPMDs occur following mechanical manipulation. Our results demonstrate that single cell TPMDs result in Ca(++) waves in neighboring keratocytes both in culture and within ex vivo corneas. The source of Ca(++) is both intra-and extra-cellular, and the signal can be mediated by ATP and/or gap junctions, and is species dependent. Stromal rubbing confirmed that TPMDs do occur following mechanical manipulation. Keratocyte TPMDs and their associated signaling events are likely common occurrences following minor or major corneal trauma. Nature Publishing Group UK 2020-02-18 /pmc/articles/PMC7029045/ /pubmed/32071321 http://dx.doi.org/10.1038/s41598-020-59570-7 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Chen, Zhong Lu, Xiaowen McGee-Lawrence, Meghan E. Watsky, Mitchell A. Transient Cell Membrane Disruptions induce Calcium Waves in Corneal Keratocytes |
title | Transient Cell Membrane Disruptions induce Calcium Waves in Corneal Keratocytes |
title_full | Transient Cell Membrane Disruptions induce Calcium Waves in Corneal Keratocytes |
title_fullStr | Transient Cell Membrane Disruptions induce Calcium Waves in Corneal Keratocytes |
title_full_unstemmed | Transient Cell Membrane Disruptions induce Calcium Waves in Corneal Keratocytes |
title_short | Transient Cell Membrane Disruptions induce Calcium Waves in Corneal Keratocytes |
title_sort | transient cell membrane disruptions induce calcium waves in corneal keratocytes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7029045/ https://www.ncbi.nlm.nih.gov/pubmed/32071321 http://dx.doi.org/10.1038/s41598-020-59570-7 |
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