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Effects of 5G-modulated 3.5 GHz radiofrequency field exposures on HSF1, RAS, ERK, and PML activation in live fibroblasts and keratinocytes cells

The potential health risks of exposure to radiofrequency electromagnetic fields from mobile communications technologies have raised societal concerns. Guidelines have been set to protect the population (e.g. non-specific heating above 1 °C under exposure to radiofrequency fields), but questions rema...

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Autores principales: Joushomme, Alexandre, Orlacchio, Rosa, Patrignoni, Lorenza, Canovi, Anne, Chappe, Yann Loïck, Poulletier De Gannes, Florence, Hurtier, Annabelle, Garenne, André, Lagroye, Isabelle, Moisan, François, Cario, Muriel, Lévêque, Philippe, Arnaud-Cormos, Delia, Percherancier, Yann
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10203668/
https://www.ncbi.nlm.nih.gov/pubmed/37221363
http://dx.doi.org/10.1038/s41598-023-35397-w
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author Joushomme, Alexandre
Orlacchio, Rosa
Patrignoni, Lorenza
Canovi, Anne
Chappe, Yann Loïck
Poulletier De Gannes, Florence
Hurtier, Annabelle
Garenne, André
Lagroye, Isabelle
Moisan, François
Cario, Muriel
Lévêque, Philippe
Arnaud-Cormos, Delia
Percherancier, Yann
author_facet Joushomme, Alexandre
Orlacchio, Rosa
Patrignoni, Lorenza
Canovi, Anne
Chappe, Yann Loïck
Poulletier De Gannes, Florence
Hurtier, Annabelle
Garenne, André
Lagroye, Isabelle
Moisan, François
Cario, Muriel
Lévêque, Philippe
Arnaud-Cormos, Delia
Percherancier, Yann
author_sort Joushomme, Alexandre
collection PubMed
description The potential health risks of exposure to radiofrequency electromagnetic fields from mobile communications technologies have raised societal concerns. Guidelines have been set to protect the population (e.g. non-specific heating above 1 °C under exposure to radiofrequency fields), but questions remain regarding the potential biological effects of non-thermal exposures. With the advent of the fifth generation (5G) of mobile communication, assessing whether exposure to this new signal induces a cellular stress response is one of the mandatory steps on the roadmap for a safe deployment and health risk evaluation. Using the BRET (Bioluminescence Resonance Energy-Transfer) technique, we assessed whether continuous or intermittent (5 min ON/ 10 min OFF) exposure of live human keratinocytes and fibroblasts cells to 5G 3.5 GHz signals at specific absorption rate (SAR) up to 4 W/kg for 24 h impact basal or chemically-induced activity of Heat Shock Factor (HSF), RAt Sarcoma virus (RAS) and Extracellular signal-Regulated Kinases (ERK) kinases, and Promyelocytic Leukemia Protein (PML), that are all molecular pathways involved in environmental cell-stress responses. The main results are (i), a decrease of the HSF1 basal BRET signal when fibroblasts cells were exposed at the lower SARs tested (0.25 and 1 W/kg), but not at the highest one (4 W/kg), and (ii) a slight decrease of As(2)O(3) maximal efficacy to trigger PML SUMOylation when fibroblasts cells, but not keratinocytes, were continuously exposed to the 5G RF-EMF signal. Nevertheless, given the inconsistency of these effects in terms of impacted cell type, effective SAR, exposure mode, and molecular cell stress response, we concluded that our study show no conclusive evidence that molecular effects can arise when skin cells are exposed to the 5G RF-EMF alone or with a chemical stressor.
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spelling pubmed-102036682023-05-25 Effects of 5G-modulated 3.5 GHz radiofrequency field exposures on HSF1, RAS, ERK, and PML activation in live fibroblasts and keratinocytes cells Joushomme, Alexandre Orlacchio, Rosa Patrignoni, Lorenza Canovi, Anne Chappe, Yann Loïck Poulletier De Gannes, Florence Hurtier, Annabelle Garenne, André Lagroye, Isabelle Moisan, François Cario, Muriel Lévêque, Philippe Arnaud-Cormos, Delia Percherancier, Yann Sci Rep Article The potential health risks of exposure to radiofrequency electromagnetic fields from mobile communications technologies have raised societal concerns. Guidelines have been set to protect the population (e.g. non-specific heating above 1 °C under exposure to radiofrequency fields), but questions remain regarding the potential biological effects of non-thermal exposures. With the advent of the fifth generation (5G) of mobile communication, assessing whether exposure to this new signal induces a cellular stress response is one of the mandatory steps on the roadmap for a safe deployment and health risk evaluation. Using the BRET (Bioluminescence Resonance Energy-Transfer) technique, we assessed whether continuous or intermittent (5 min ON/ 10 min OFF) exposure of live human keratinocytes and fibroblasts cells to 5G 3.5 GHz signals at specific absorption rate (SAR) up to 4 W/kg for 24 h impact basal or chemically-induced activity of Heat Shock Factor (HSF), RAt Sarcoma virus (RAS) and Extracellular signal-Regulated Kinases (ERK) kinases, and Promyelocytic Leukemia Protein (PML), that are all molecular pathways involved in environmental cell-stress responses. The main results are (i), a decrease of the HSF1 basal BRET signal when fibroblasts cells were exposed at the lower SARs tested (0.25 and 1 W/kg), but not at the highest one (4 W/kg), and (ii) a slight decrease of As(2)O(3) maximal efficacy to trigger PML SUMOylation when fibroblasts cells, but not keratinocytes, were continuously exposed to the 5G RF-EMF signal. Nevertheless, given the inconsistency of these effects in terms of impacted cell type, effective SAR, exposure mode, and molecular cell stress response, we concluded that our study show no conclusive evidence that molecular effects can arise when skin cells are exposed to the 5G RF-EMF alone or with a chemical stressor. Nature Publishing Group UK 2023-05-23 /pmc/articles/PMC10203668/ /pubmed/37221363 http://dx.doi.org/10.1038/s41598-023-35397-w Text en © The Author(s) 2023 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
Joushomme, Alexandre
Orlacchio, Rosa
Patrignoni, Lorenza
Canovi, Anne
Chappe, Yann Loïck
Poulletier De Gannes, Florence
Hurtier, Annabelle
Garenne, André
Lagroye, Isabelle
Moisan, François
Cario, Muriel
Lévêque, Philippe
Arnaud-Cormos, Delia
Percherancier, Yann
Effects of 5G-modulated 3.5 GHz radiofrequency field exposures on HSF1, RAS, ERK, and PML activation in live fibroblasts and keratinocytes cells
title Effects of 5G-modulated 3.5 GHz radiofrequency field exposures on HSF1, RAS, ERK, and PML activation in live fibroblasts and keratinocytes cells
title_full Effects of 5G-modulated 3.5 GHz radiofrequency field exposures on HSF1, RAS, ERK, and PML activation in live fibroblasts and keratinocytes cells
title_fullStr Effects of 5G-modulated 3.5 GHz radiofrequency field exposures on HSF1, RAS, ERK, and PML activation in live fibroblasts and keratinocytes cells
title_full_unstemmed Effects of 5G-modulated 3.5 GHz radiofrequency field exposures on HSF1, RAS, ERK, and PML activation in live fibroblasts and keratinocytes cells
title_short Effects of 5G-modulated 3.5 GHz radiofrequency field exposures on HSF1, RAS, ERK, and PML activation in live fibroblasts and keratinocytes cells
title_sort effects of 5g-modulated 3.5 ghz radiofrequency field exposures on hsf1, ras, erk, and pml activation in live fibroblasts and keratinocytes cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10203668/
https://www.ncbi.nlm.nih.gov/pubmed/37221363
http://dx.doi.org/10.1038/s41598-023-35397-w
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