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Effects of Cold Atmospheric Plasma (CAP) on ß-Defensins, Inflammatory Cytokines, and Apoptosis-Related Molecules in Keratinocytes In Vitro and In Vivo

Cold atmospheric plasma (CAP) has been gaining increasing interest as a new approach for the treatment of skin diseases or wounds. Although this approach has demonstrated promising antibacterial activity, its exact mechanism of action remains unclear. This study explored in vitro and in vivo whether...

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Autores principales: Arndt, Stephanie, Landthaler, Michael, Zimmermann, Julia L., Unger, Petra, Wacker, Eva, Shimizu, Tetsuji, Li, Yang-Fang, Morfill, Gregor E., Bosserhoff, Anja-Katrin, Karrer, Sigrid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4359157/
https://www.ncbi.nlm.nih.gov/pubmed/25768736
http://dx.doi.org/10.1371/journal.pone.0120041
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author Arndt, Stephanie
Landthaler, Michael
Zimmermann, Julia L.
Unger, Petra
Wacker, Eva
Shimizu, Tetsuji
Li, Yang-Fang
Morfill, Gregor E.
Bosserhoff, Anja-Katrin
Karrer, Sigrid
author_facet Arndt, Stephanie
Landthaler, Michael
Zimmermann, Julia L.
Unger, Petra
Wacker, Eva
Shimizu, Tetsuji
Li, Yang-Fang
Morfill, Gregor E.
Bosserhoff, Anja-Katrin
Karrer, Sigrid
author_sort Arndt, Stephanie
collection PubMed
description Cold atmospheric plasma (CAP) has been gaining increasing interest as a new approach for the treatment of skin diseases or wounds. Although this approach has demonstrated promising antibacterial activity, its exact mechanism of action remains unclear. This study explored in vitro and in vivo whether CAP influences gene expression and molecular mechanisms in keratinocytes. Our results revealed that a 2 min CAP treatment using the MicroPlaSter ß in analogy to the performed clinical studies for wound treatment induces expression of IL-8, TGF-ß1, and TGF-ß2. In vitro and in vivo assays indicated that keratinocyte proliferation, migration, and apoptotic mechanisms were not affected by the CAP treatment under the applied conditions. Further, we observed that antimicrobial peptides of the ß-defensin family are upregulated after CAP treatment. In summary, our results suggest that a 2 min application of CAP induces gene expression of key regulators important for inflammation and wound healing without causing proliferation, migration or cell death in keratinocytes. The induction of ß-defensins in keratinocytes describes an absolutely new plasma strategy. Activation of antimicrobial peptides supports the well-known antibacterial effect of CAP treatment, whereas the mechanism of ß-defensin activation by CAP is not investigated so far.
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spelling pubmed-43591572015-03-23 Effects of Cold Atmospheric Plasma (CAP) on ß-Defensins, Inflammatory Cytokines, and Apoptosis-Related Molecules in Keratinocytes In Vitro and In Vivo Arndt, Stephanie Landthaler, Michael Zimmermann, Julia L. Unger, Petra Wacker, Eva Shimizu, Tetsuji Li, Yang-Fang Morfill, Gregor E. Bosserhoff, Anja-Katrin Karrer, Sigrid PLoS One Research Article Cold atmospheric plasma (CAP) has been gaining increasing interest as a new approach for the treatment of skin diseases or wounds. Although this approach has demonstrated promising antibacterial activity, its exact mechanism of action remains unclear. This study explored in vitro and in vivo whether CAP influences gene expression and molecular mechanisms in keratinocytes. Our results revealed that a 2 min CAP treatment using the MicroPlaSter ß in analogy to the performed clinical studies for wound treatment induces expression of IL-8, TGF-ß1, and TGF-ß2. In vitro and in vivo assays indicated that keratinocyte proliferation, migration, and apoptotic mechanisms were not affected by the CAP treatment under the applied conditions. Further, we observed that antimicrobial peptides of the ß-defensin family are upregulated after CAP treatment. In summary, our results suggest that a 2 min application of CAP induces gene expression of key regulators important for inflammation and wound healing without causing proliferation, migration or cell death in keratinocytes. The induction of ß-defensins in keratinocytes describes an absolutely new plasma strategy. Activation of antimicrobial peptides supports the well-known antibacterial effect of CAP treatment, whereas the mechanism of ß-defensin activation by CAP is not investigated so far. Public Library of Science 2015-03-13 /pmc/articles/PMC4359157/ /pubmed/25768736 http://dx.doi.org/10.1371/journal.pone.0120041 Text en © 2015 Arndt 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Arndt, Stephanie
Landthaler, Michael
Zimmermann, Julia L.
Unger, Petra
Wacker, Eva
Shimizu, Tetsuji
Li, Yang-Fang
Morfill, Gregor E.
Bosserhoff, Anja-Katrin
Karrer, Sigrid
Effects of Cold Atmospheric Plasma (CAP) on ß-Defensins, Inflammatory Cytokines, and Apoptosis-Related Molecules in Keratinocytes In Vitro and In Vivo
title Effects of Cold Atmospheric Plasma (CAP) on ß-Defensins, Inflammatory Cytokines, and Apoptosis-Related Molecules in Keratinocytes In Vitro and In Vivo
title_full Effects of Cold Atmospheric Plasma (CAP) on ß-Defensins, Inflammatory Cytokines, and Apoptosis-Related Molecules in Keratinocytes In Vitro and In Vivo
title_fullStr Effects of Cold Atmospheric Plasma (CAP) on ß-Defensins, Inflammatory Cytokines, and Apoptosis-Related Molecules in Keratinocytes In Vitro and In Vivo
title_full_unstemmed Effects of Cold Atmospheric Plasma (CAP) on ß-Defensins, Inflammatory Cytokines, and Apoptosis-Related Molecules in Keratinocytes In Vitro and In Vivo
title_short Effects of Cold Atmospheric Plasma (CAP) on ß-Defensins, Inflammatory Cytokines, and Apoptosis-Related Molecules in Keratinocytes In Vitro and In Vivo
title_sort effects of cold atmospheric plasma (cap) on ß-defensins, inflammatory cytokines, and apoptosis-related molecules in keratinocytes in vitro and in vivo
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4359157/
https://www.ncbi.nlm.nih.gov/pubmed/25768736
http://dx.doi.org/10.1371/journal.pone.0120041
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