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Effect of 1-MHz ultrasound on the proinflammatory interleukin-6 secretion in human keratinocytes

Keratinocytes, the main cell type of the skin, are one of the most exposed cells to environmental factors, providing a first defence barrier for the host and actively participating in immune response. In fact, keratinocytes express pattern recognition receptors that interact with pathogen associated...

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Autores principales: Giantulli, Sabrina, Tortorella, Elisabetta, Brasili, Francesco, Scarpa, Susanna, Cerroni, Barbara, Paradossi, Gaio, Bedini, Angelico, Morrone, Stefania, Silvestri, Ida, Domenici, Fabio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8463532/
https://www.ncbi.nlm.nih.gov/pubmed/34561481
http://dx.doi.org/10.1038/s41598-021-98141-2
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author Giantulli, Sabrina
Tortorella, Elisabetta
Brasili, Francesco
Scarpa, Susanna
Cerroni, Barbara
Paradossi, Gaio
Bedini, Angelico
Morrone, Stefania
Silvestri, Ida
Domenici, Fabio
author_facet Giantulli, Sabrina
Tortorella, Elisabetta
Brasili, Francesco
Scarpa, Susanna
Cerroni, Barbara
Paradossi, Gaio
Bedini, Angelico
Morrone, Stefania
Silvestri, Ida
Domenici, Fabio
author_sort Giantulli, Sabrina
collection PubMed
description Keratinocytes, the main cell type of the skin, are one of the most exposed cells to environmental factors, providing a first defence barrier for the host and actively participating in immune response. In fact, keratinocytes express pattern recognition receptors that interact with pathogen associated molecular patterns and damage associated molecular patterns, leading to the production of cytokines and chemokines, including interleukin (IL)-6. Herein, we investigated whether mechanical energy transported by low intensity ultrasound (US) could generate a mechanical stress able to induce the release of inflammatory cytokine such IL-6 in the human keratinocyte cell line, HaCaT. The extensive clinical application of US in both diagnosis and therapy suggests the need to better understand the related biological effects. Our results point out that US promotes the overexpression and secretion of IL-6, associated with the activation of nuclear factor-κB (NF-κB). Furthermore, we observed a reduced cell viability dependent on exposure parameters together with alterations in membrane permeability, paving the way for further investigating the molecular mechanisms related to US exposure.
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spelling pubmed-84635322021-09-27 Effect of 1-MHz ultrasound on the proinflammatory interleukin-6 secretion in human keratinocytes Giantulli, Sabrina Tortorella, Elisabetta Brasili, Francesco Scarpa, Susanna Cerroni, Barbara Paradossi, Gaio Bedini, Angelico Morrone, Stefania Silvestri, Ida Domenici, Fabio Sci Rep Article Keratinocytes, the main cell type of the skin, are one of the most exposed cells to environmental factors, providing a first defence barrier for the host and actively participating in immune response. In fact, keratinocytes express pattern recognition receptors that interact with pathogen associated molecular patterns and damage associated molecular patterns, leading to the production of cytokines and chemokines, including interleukin (IL)-6. Herein, we investigated whether mechanical energy transported by low intensity ultrasound (US) could generate a mechanical stress able to induce the release of inflammatory cytokine such IL-6 in the human keratinocyte cell line, HaCaT. The extensive clinical application of US in both diagnosis and therapy suggests the need to better understand the related biological effects. Our results point out that US promotes the overexpression and secretion of IL-6, associated with the activation of nuclear factor-κB (NF-κB). Furthermore, we observed a reduced cell viability dependent on exposure parameters together with alterations in membrane permeability, paving the way for further investigating the molecular mechanisms related to US exposure. Nature Publishing Group UK 2021-09-24 /pmc/articles/PMC8463532/ /pubmed/34561481 http://dx.doi.org/10.1038/s41598-021-98141-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Giantulli, Sabrina
Tortorella, Elisabetta
Brasili, Francesco
Scarpa, Susanna
Cerroni, Barbara
Paradossi, Gaio
Bedini, Angelico
Morrone, Stefania
Silvestri, Ida
Domenici, Fabio
Effect of 1-MHz ultrasound on the proinflammatory interleukin-6 secretion in human keratinocytes
title Effect of 1-MHz ultrasound on the proinflammatory interleukin-6 secretion in human keratinocytes
title_full Effect of 1-MHz ultrasound on the proinflammatory interleukin-6 secretion in human keratinocytes
title_fullStr Effect of 1-MHz ultrasound on the proinflammatory interleukin-6 secretion in human keratinocytes
title_full_unstemmed Effect of 1-MHz ultrasound on the proinflammatory interleukin-6 secretion in human keratinocytes
title_short Effect of 1-MHz ultrasound on the proinflammatory interleukin-6 secretion in human keratinocytes
title_sort effect of 1-mhz ultrasound on the proinflammatory interleukin-6 secretion in human keratinocytes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8463532/
https://www.ncbi.nlm.nih.gov/pubmed/34561481
http://dx.doi.org/10.1038/s41598-021-98141-2
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