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Cold atmospheric plasma causes a calcium influx in melanoma cells triggering CAP-induced senescence

Cold atmospheric plasma (CAP) is a promising approach in anti-cancer therapy, eliminating cancer cells with high selectivity. However, the molecular mechanisms of CAP action are poorly understood. In this study, we investigated CAP effects on calcium homeostasis in melanoma cells. We observed increa...

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Autores principales: Schneider, Christin, Gebhardt, Lisa, Arndt, Stephanie, Karrer, Sigrid, Zimmermann, Julia L., Fischer, Michael J. M., Bosserhoff, Anja-Katrin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6030087/
https://www.ncbi.nlm.nih.gov/pubmed/29968804
http://dx.doi.org/10.1038/s41598-018-28443-5
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author Schneider, Christin
Gebhardt, Lisa
Arndt, Stephanie
Karrer, Sigrid
Zimmermann, Julia L.
Fischer, Michael J. M.
Bosserhoff, Anja-Katrin
author_facet Schneider, Christin
Gebhardt, Lisa
Arndt, Stephanie
Karrer, Sigrid
Zimmermann, Julia L.
Fischer, Michael J. M.
Bosserhoff, Anja-Katrin
author_sort Schneider, Christin
collection PubMed
description Cold atmospheric plasma (CAP) is a promising approach in anti-cancer therapy, eliminating cancer cells with high selectivity. However, the molecular mechanisms of CAP action are poorly understood. In this study, we investigated CAP effects on calcium homeostasis in melanoma cells. We observed increased cytoplasmic calcium after CAP treatment, which also occurred in the absence of extracellular calcium, indicating the majority of the calcium increase originates from intracellular stores. Application of previously CAP-exposed extracellular solutions also induced cytoplasmic calcium elevations. A substantial fraction of this effect remained when the application was delayed for one hour, indicating the chemical stability of the activating agent(s). Addition of ryanodine and cyclosporin A indicate the involvement of the endoplasmatic reticulum and the mitochondria. Inhibition of the cytoplasmic calcium elevation by the intracellular chelator BAPTA blocked CAP-induced senescence. This finding helps to understand the molecular influence and the mode of action of CAP on tumor cells.
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spelling pubmed-60300872018-07-11 Cold atmospheric plasma causes a calcium influx in melanoma cells triggering CAP-induced senescence Schneider, Christin Gebhardt, Lisa Arndt, Stephanie Karrer, Sigrid Zimmermann, Julia L. Fischer, Michael J. M. Bosserhoff, Anja-Katrin Sci Rep Article Cold atmospheric plasma (CAP) is a promising approach in anti-cancer therapy, eliminating cancer cells with high selectivity. However, the molecular mechanisms of CAP action are poorly understood. In this study, we investigated CAP effects on calcium homeostasis in melanoma cells. We observed increased cytoplasmic calcium after CAP treatment, which also occurred in the absence of extracellular calcium, indicating the majority of the calcium increase originates from intracellular stores. Application of previously CAP-exposed extracellular solutions also induced cytoplasmic calcium elevations. A substantial fraction of this effect remained when the application was delayed for one hour, indicating the chemical stability of the activating agent(s). Addition of ryanodine and cyclosporin A indicate the involvement of the endoplasmatic reticulum and the mitochondria. Inhibition of the cytoplasmic calcium elevation by the intracellular chelator BAPTA blocked CAP-induced senescence. This finding helps to understand the molecular influence and the mode of action of CAP on tumor cells. Nature Publishing Group UK 2018-07-03 /pmc/articles/PMC6030087/ /pubmed/29968804 http://dx.doi.org/10.1038/s41598-018-28443-5 Text en © The Author(s) 2018 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
Schneider, Christin
Gebhardt, Lisa
Arndt, Stephanie
Karrer, Sigrid
Zimmermann, Julia L.
Fischer, Michael J. M.
Bosserhoff, Anja-Katrin
Cold atmospheric plasma causes a calcium influx in melanoma cells triggering CAP-induced senescence
title Cold atmospheric plasma causes a calcium influx in melanoma cells triggering CAP-induced senescence
title_full Cold atmospheric plasma causes a calcium influx in melanoma cells triggering CAP-induced senescence
title_fullStr Cold atmospheric plasma causes a calcium influx in melanoma cells triggering CAP-induced senescence
title_full_unstemmed Cold atmospheric plasma causes a calcium influx in melanoma cells triggering CAP-induced senescence
title_short Cold atmospheric plasma causes a calcium influx in melanoma cells triggering CAP-induced senescence
title_sort cold atmospheric plasma causes a calcium influx in melanoma cells triggering cap-induced senescence
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6030087/
https://www.ncbi.nlm.nih.gov/pubmed/29968804
http://dx.doi.org/10.1038/s41598-018-28443-5
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