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 in | International journal of molecular sciences Vol. 23; no. 2; p. 658 |
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Main Authors | , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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08.01.2022
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ISSN | 1422-0067 1661-6596 1422-0067 |
DOI | 10.3390/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. |
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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.) |
AuthorAffiliation_xml | – name: 3 Paris Sciences et Lettres Research University, F-75006 Paris, France – name: 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.) – name: 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.) – name: 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.) – name: 5 Institut Universitaire de France (IUF), F-75005 Paris, France |
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CitedBy_id | crossref_primary_10_3390_bios13080763 crossref_primary_10_1002_bem_22543 crossref_primary_10_1016_j_scitotenv_2024_176023 crossref_primary_10_1038_s41598_023_35397_w |
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Keywords | rat cortex primary cells autophagy digital holographic microscopy apoptosis human cell lines bioelectromagnetics radiofrequency electromagnetic fields impedancemetry label-free techniques |
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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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