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Apoptotic Effect of 1800 MHz Electromagnetic Radiation on NIH/3T3 Cells
To investigate the effect of 1800 MHz electromagnetic radiation (EMR) on apoptosis, we exposed NIH/3T3 cells at 1800 MHz with a specific absorption rate (SAR) of 2 W/kg intermittently for 12, 24, 36, and 48 h. After exposure, Cell Counting Kit-8 (CCK-8) and flow cytometry were used to detect cell vi...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7037840/ https://www.ncbi.nlm.nih.gov/pubmed/32013005 http://dx.doi.org/10.3390/ijerph17030819 |
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author | Li, Dan-Yang Song, Jing-Dong Liang, Zhao-Yuan Oskouei, Kiana Xiao, Xiang-Qian Hou, Wen-Zhe Li, Jin-Tao Yang, Yi-Shu Wang, Ming-Lian Murbach, Manuel |
author_facet | Li, Dan-Yang Song, Jing-Dong Liang, Zhao-Yuan Oskouei, Kiana Xiao, Xiang-Qian Hou, Wen-Zhe Li, Jin-Tao Yang, Yi-Shu Wang, Ming-Lian Murbach, Manuel |
author_sort | Li, Dan-Yang |
collection | PubMed |
description | To investigate the effect of 1800 MHz electromagnetic radiation (EMR) on apoptosis, we exposed NIH/3T3 cells at 1800 MHz with a specific absorption rate (SAR) of 2 W/kg intermittently for 12, 24, 36, and 48 h. After exposure, Cell Counting Kit-8 (CCK-8) and flow cytometry were used to detect cell viability and apoptosis; the expression of p53, a molecule with the key role in apoptosis, was measured by real-time qPCR, western blot, and immunofluorescence; and images of the structure of the mitochondria, directly reflecting apoptosis, were captured by electron microscopy. The results showed that the viability of cells in the 12, 36, and 48 h exposure groups significantly decreased compared with the sham groups; after 48 h of exposure, the percentage of late apoptotic cells in the exposure group was significantly higher. Real-time qPCR results showed that p53 mRNA in the 48 h exposure group was 1.4-fold of that in the sham group; significant differences of p53 protein fluorescence expression were observed between the exposure groups and the sham groups after 24 h and 48 h. The mitochondrial swelling and vesicular morphology were found in the electron microscopy images after 48 h exposure. These findings demonstrated 1800 MHz, SAR 2 W/kg EMR for 48 h may cause apoptosis in NIH/3T3 cells and that this apoptosis might be attributed to mitochondrial damage and upregulation of p53 expression. |
format | Online Article Text |
id | pubmed-7037840 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-70378402020-03-10 Apoptotic Effect of 1800 MHz Electromagnetic Radiation on NIH/3T3 Cells Li, Dan-Yang Song, Jing-Dong Liang, Zhao-Yuan Oskouei, Kiana Xiao, Xiang-Qian Hou, Wen-Zhe Li, Jin-Tao Yang, Yi-Shu Wang, Ming-Lian Murbach, Manuel Int J Environ Res Public Health Article To investigate the effect of 1800 MHz electromagnetic radiation (EMR) on apoptosis, we exposed NIH/3T3 cells at 1800 MHz with a specific absorption rate (SAR) of 2 W/kg intermittently for 12, 24, 36, and 48 h. After exposure, Cell Counting Kit-8 (CCK-8) and flow cytometry were used to detect cell viability and apoptosis; the expression of p53, a molecule with the key role in apoptosis, was measured by real-time qPCR, western blot, and immunofluorescence; and images of the structure of the mitochondria, directly reflecting apoptosis, were captured by electron microscopy. The results showed that the viability of cells in the 12, 36, and 48 h exposure groups significantly decreased compared with the sham groups; after 48 h of exposure, the percentage of late apoptotic cells in the exposure group was significantly higher. Real-time qPCR results showed that p53 mRNA in the 48 h exposure group was 1.4-fold of that in the sham group; significant differences of p53 protein fluorescence expression were observed between the exposure groups and the sham groups after 24 h and 48 h. The mitochondrial swelling and vesicular morphology were found in the electron microscopy images after 48 h exposure. These findings demonstrated 1800 MHz, SAR 2 W/kg EMR for 48 h may cause apoptosis in NIH/3T3 cells and that this apoptosis might be attributed to mitochondrial damage and upregulation of p53 expression. MDPI 2020-01-28 2020-02 /pmc/articles/PMC7037840/ /pubmed/32013005 http://dx.doi.org/10.3390/ijerph17030819 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Li, Dan-Yang Song, Jing-Dong Liang, Zhao-Yuan Oskouei, Kiana Xiao, Xiang-Qian Hou, Wen-Zhe Li, Jin-Tao Yang, Yi-Shu Wang, Ming-Lian Murbach, Manuel Apoptotic Effect of 1800 MHz Electromagnetic Radiation on NIH/3T3 Cells |
title | Apoptotic Effect of 1800 MHz Electromagnetic Radiation on NIH/3T3 Cells |
title_full | Apoptotic Effect of 1800 MHz Electromagnetic Radiation on NIH/3T3 Cells |
title_fullStr | Apoptotic Effect of 1800 MHz Electromagnetic Radiation on NIH/3T3 Cells |
title_full_unstemmed | Apoptotic Effect of 1800 MHz Electromagnetic Radiation on NIH/3T3 Cells |
title_short | Apoptotic Effect of 1800 MHz Electromagnetic Radiation on NIH/3T3 Cells |
title_sort | apoptotic effect of 1800 mhz electromagnetic radiation on nih/3t3 cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7037840/ https://www.ncbi.nlm.nih.gov/pubmed/32013005 http://dx.doi.org/10.3390/ijerph17030819 |
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