Label-Free Study of the Global Cell Behavior during Exposure to Environmental Radiofrequency Fields in the Presence or Absence of Pro-Apoptotic or Pro-Autophagic Treatments

It remains controversial whether exposure to environmental radiofrequency signals (RF) impacts cell status or response to cellular stress such as apoptosis or autophagy. We used two label-free techniques, cellular impedancemetry and Digital Holographic Microscopy (DHM), to assess the overall cellula...

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Published inInternational journal of molecular sciences Vol. 23; no. 2; p. 658
Main Authors Joushomme, Alexandre, Garenne, André, Dufossée, Mélody, Renom, Rémy, Ruigrok, Hermanus Johannes, Chappe, Yann Loick, Canovi, Anne, Patrignoni, Lorenza, Hurtier, Annabelle, Poulletier de Gannes, Florence, Lagroye, Isabelle, Lévêque, Philippe, Lewis, Noëlle, Priault, Muriel, Arnaud-Cormos, Delia, Percherancier, Yann
Format Journal Article
LanguageEnglish
Published Switzerland MDPI AG 08.01.2022
MDPI
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ISSN1422-0067
1661-6596
1422-0067
DOI10.3390/ijms23020658

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Abstract It remains controversial whether exposure to environmental radiofrequency signals (RF) impacts cell status or response to cellular stress such as apoptosis or autophagy. We used two label-free techniques, cellular impedancemetry and Digital Holographic Microscopy (DHM), to assess the overall cellular response during RF exposure alone, or during co-exposure to RF and chemical treatments known to induce either apoptosis or autophagy. Two human cell lines (SH-SY5Y and HCT116) and two cultures of primary rat cortex cells (astrocytes and co-culture of neurons and glial cells) were exposed to RF using an 1800 MHz carrier wave modulated with various environmental signals (GSM: Global System for Mobile Communications, 2G signal), UMTS (Universal Mobile Telecommunications System, 3G signal), LTE (Long-Term Evolution, 4G signal, and Wi-Fi) or unmodulated RF (continuous wave, CW). The specific absorption rates (S.A.R.) used were 1.5 and 6 W/kg during DHM experiments and ranged from 5 to 24 W/kg during the recording of cellular impedance. Cells were continuously exposed for three to five consecutive days while the temporal phenotypic signature of cells behavior was recorded at constant temperature. Statistical analysis of the results does not indicate that RF-EMF exposure impacted the global behavior of healthy, apoptotic, or autophagic cells, even at S.A.R. levels higher than the guidelines, provided that the temperature was kept constant.
AbstractList It remains controversial whether exposure to environmental radiofrequency signals (RF) impacts cell status or response to cellular stress such as apoptosis or autophagy. We used two label-free techniques, cellular impedancemetry and Digital Holographic Microscopy (DHM), to assess the overall cellular response during RF exposure alone, or during co-exposure to RF and chemical treatments known to induce either apoptosis or autophagy. Two human cell lines (SH-SY5Y and HCT116) and two cultures of primary rat cortex cells (astrocytes and co-culture of neurons and glial cells) were exposed to RF using an 1800 MHz carrier wave modulated with various environmental signals (GSM: Global System for Mobile Communications, 2G signal), UMTS (Universal Mobile Telecommunications System, 3G signal), LTE (Long-Term Evolution, 4G signal, and Wi-Fi) or unmodulated RF (continuous wave, CW). The specific absorption rates (S.A.R.) used were 1.5 and 6 W/kg during DHM experiments and ranged from 5 to 24 W/kg during the recording of cellular impedance. Cells were continuously exposed for three to five consecutive days while the temporal phenotypic signature of cells behavior was recorded at constant temperature. Statistical analysis of the results does not indicate that RF-EMF exposure impacted the global behavior of healthy, apoptotic, or autophagic cells, even at S.A.R. levels higher than the guidelines, provided that the temperature was kept constant.
It remains controversial whether exposure to environmental radiofrequency signals (RF) impacts cell status or response to cellular stress such as apoptosis or autophagy. We used two label-free techniques, cellular impedancemetry and Digital Holographic Microscopy (DHM), to assess the overall cellular response during RF exposure alone, or during co-exposure to RF and chemical treatments known to induce either apoptosis or autophagy. Two human cell lines (SH-SY5Y and HCT116) and two cultures of primary rat cortex cells (astrocytes and co-culture of neurons and glial cells) were exposed to RF using an 1800 MHz carrier wave modulated with various environmental signals (GSM: Global System for Mobile Communications, 2G signal), UMTS (Universal Mobile Telecommunications System, 3G signal), LTE (Long-Term Evolution, 4G signal, and Wi-Fi) or unmodulated RF (continuous wave, CW). The specific absorption rates (S.A.R.) used were 1.5 and 6 W/kg during DHM experiments and ranged from 5 to 24 W/kg during the recording of cellular impedance. Cells were continuously exposed for three to five consecutive days while the temporal phenotypic signature of cells behavior was recorded at constant temperature. Statistical analysis of the results does not indicate that RF-EMF exposure impacted the global behavior of healthy, apoptotic, or autophagic cells, even at S.A.R. levels higher than the guidelines, provided that the temperature was kept constant.It remains controversial whether exposure to environmental radiofrequency signals (RF) impacts cell status or response to cellular stress such as apoptosis or autophagy. We used two label-free techniques, cellular impedancemetry and Digital Holographic Microscopy (DHM), to assess the overall cellular response during RF exposure alone, or during co-exposure to RF and chemical treatments known to induce either apoptosis or autophagy. Two human cell lines (SH-SY5Y and HCT116) and two cultures of primary rat cortex cells (astrocytes and co-culture of neurons and glial cells) were exposed to RF using an 1800 MHz carrier wave modulated with various environmental signals (GSM: Global System for Mobile Communications, 2G signal), UMTS (Universal Mobile Telecommunications System, 3G signal), LTE (Long-Term Evolution, 4G signal, and Wi-Fi) or unmodulated RF (continuous wave, CW). The specific absorption rates (S.A.R.) used were 1.5 and 6 W/kg during DHM experiments and ranged from 5 to 24 W/kg during the recording of cellular impedance. Cells were continuously exposed for three to five consecutive days while the temporal phenotypic signature of cells behavior was recorded at constant temperature. Statistical analysis of the results does not indicate that RF-EMF exposure impacted the global behavior of healthy, apoptotic, or autophagic cells, even at S.A.R. levels higher than the guidelines, provided that the temperature was kept constant.
Author Garenne, André
Dufossée, Mélody
Joushomme, Alexandre
Patrignoni, Lorenza
Ruigrok, Hermanus Johannes
Lévêque, Philippe
Percherancier, Yann
Lagroye, Isabelle
Hurtier, Annabelle
Lewis, Noëlle
Priault, Muriel
Poulletier de Gannes, Florence
Arnaud-Cormos, Delia
Canovi, Anne
Chappe, Yann Loick
Renom, Rémy
AuthorAffiliation 3 Paris Sciences et Lettres Research University, F-75006 Paris, France
5 Institut Universitaire de France (IUF), F-75005 Paris, France
4 Univ. Limoges, CNRS, XLIM/UMR 7252, F-87000 Limoges, France; philippe.leveque@unilim.fr (P.L.); delia.arnaud-cormos@unilim.fr (D.A.-C.)
2 Univ. Bordeaux, CNRS, IBGC/UMR 5095, F-33000 Bordeaux, France; melody.dufossee@ibgc.cnrs.fr (M.D.); muriel.priault@ibgc.cnrs.fr (M.P.)
1 Univ. Bordeaux, CNRS, IMS/UMR 5218, F-33400 Talence, France; alexandre.joushomme@u-bordeaux.fr (A.J.); andre.garenne@u-bordeaux.fr (A.G.); remy330@msn.com (R.R.); hruigrok@sebia.com (H.J.R.); yann.chappe@u-bordeaux.fr (Y.L.C.); anne.canovi@u-bordeaux.fr (A.C.); lorenza.patrignoni@u-bordeaux.fr (L.P.); annabelle.hurtier@ims-bordeaux.fr (A.H.); florence.poulletier@ims-bordeaux.fr (F.P.d.G.); isabelle.lagroye@ephe.psl.eu (I.L.); noelle.lewis@u-bordeaux.fr (N.L.)
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Issue 2
Keywords rat cortex primary cells
autophagy
digital holographic microscopy
apoptosis
human cell lines
bioelectromagnetics
radiofrequency electromagnetic fields
impedancemetry
label-free techniques
Language English
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Snippet It remains controversial whether exposure to environmental radiofrequency signals (RF) impacts cell status or response to cellular stress such as apoptosis or...
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StartPage 658
SubjectTerms Apoptosis
Arsenic Trioxide - pharmacology
Astrocytes - drug effects
Astrocytes - pathology
Autophagy - drug effects
Cell Line, Tumor
Culture Media, Serum-Free
Electric Impedance
Experiments
Holography
Humans
Life Sciences
Neuroblastoma
Neurons - drug effects
Neurons - pathology
Radio Waves
Staining and Labeling
Telecommunications systems
Time Factors
Toxicity
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Title Label-Free Study of the Global Cell Behavior during Exposure to Environmental Radiofrequency Fields in the Presence or Absence of Pro-Apoptotic or Pro-Autophagic Treatments
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