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Effects of Electromagnetic Waves with LTE and 5G Bandwidth on the Skin Pigmentation In Vitro
With the rapid growth of wireless communication devices, the influences of electromagnetic fields (EMF) on human health are gathering increasing attention. Since the skin is the largest organ of the body and is located at the outermost layer, it is considered a major target for the health effects of...
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/PMC7794711/ https://www.ncbi.nlm.nih.gov/pubmed/33375304 http://dx.doi.org/10.3390/ijms22010170 |
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author | Kim, Kyuri Lee, Young Seung Kim, Nam Choi, Hyung-Do Kang, Dong-Jun Kim, Hak Rim Lim, Kyung-Min |
author_facet | Kim, Kyuri Lee, Young Seung Kim, Nam Choi, Hyung-Do Kang, Dong-Jun Kim, Hak Rim Lim, Kyung-Min |
author_sort | Kim, Kyuri |
collection | PubMed |
description | With the rapid growth of wireless communication devices, the influences of electromagnetic fields (EMF) on human health are gathering increasing attention. Since the skin is the largest organ of the body and is located at the outermost layer, it is considered a major target for the health effects of EMF. Skin pigmentation represents one of the most frequent symptoms caused by various non-ionizing radiations, including ultraviolet radiation, blue light, infrared, and extremely low frequency (ELF). Here, we investigated the effects of EMFs with long-term evolution (LTE, 1.762 GHz) and 5G (28 GHz) bandwidth on skin pigmentation in vitro. Murine and Human melanoma cells (B16F10 and MNT-1) were exposed to either LTE or 5G for 4 h per day, which is considered the upper bound of average smartphone use time. It was shown that neither LTE nor 5G exposure induced significant effects on cell viability or pigmentation. The dendrites of MNT-1 were neither lengthened nor regressed after EMF exposure. Skin pigmentation effects of EMFs were further examined in the human keratinocyte cell line (MNT-1-HaCaT) co-culture system, which confirmed the absence of significant hyper-pigmentation effects of LTE and 5G EMFs. Lastly, MelanoDerm™, a 3D pigmented human epidermis model, was irradiated with LTE (1.762 GHz) or 5G (28 GHz), and image analysis and special staining were performed. No changes in the brightness of MelanoDerm™ tissues were observed in LTE- or 5G-exposed tissues, except for only minimal changes in the size of melanocytes. Collectively, these results imply that exposure to LTE and 5G EMFs may not affect melanin synthesis or skin pigmentation under normal smartphone use condition. |
format | Online Article Text |
id | pubmed-7794711 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-77947112021-01-10 Effects of Electromagnetic Waves with LTE and 5G Bandwidth on the Skin Pigmentation In Vitro Kim, Kyuri Lee, Young Seung Kim, Nam Choi, Hyung-Do Kang, Dong-Jun Kim, Hak Rim Lim, Kyung-Min Int J Mol Sci Article With the rapid growth of wireless communication devices, the influences of electromagnetic fields (EMF) on human health are gathering increasing attention. Since the skin is the largest organ of the body and is located at the outermost layer, it is considered a major target for the health effects of EMF. Skin pigmentation represents one of the most frequent symptoms caused by various non-ionizing radiations, including ultraviolet radiation, blue light, infrared, and extremely low frequency (ELF). Here, we investigated the effects of EMFs with long-term evolution (LTE, 1.762 GHz) and 5G (28 GHz) bandwidth on skin pigmentation in vitro. Murine and Human melanoma cells (B16F10 and MNT-1) were exposed to either LTE or 5G for 4 h per day, which is considered the upper bound of average smartphone use time. It was shown that neither LTE nor 5G exposure induced significant effects on cell viability or pigmentation. The dendrites of MNT-1 were neither lengthened nor regressed after EMF exposure. Skin pigmentation effects of EMFs were further examined in the human keratinocyte cell line (MNT-1-HaCaT) co-culture system, which confirmed the absence of significant hyper-pigmentation effects of LTE and 5G EMFs. Lastly, MelanoDerm™, a 3D pigmented human epidermis model, was irradiated with LTE (1.762 GHz) or 5G (28 GHz), and image analysis and special staining were performed. No changes in the brightness of MelanoDerm™ tissues were observed in LTE- or 5G-exposed tissues, except for only minimal changes in the size of melanocytes. Collectively, these results imply that exposure to LTE and 5G EMFs may not affect melanin synthesis or skin pigmentation under normal smartphone use condition. MDPI 2020-12-26 /pmc/articles/PMC7794711/ /pubmed/33375304 http://dx.doi.org/10.3390/ijms22010170 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 Kim, Kyuri Lee, Young Seung Kim, Nam Choi, Hyung-Do Kang, Dong-Jun Kim, Hak Rim Lim, Kyung-Min Effects of Electromagnetic Waves with LTE and 5G Bandwidth on the Skin Pigmentation In Vitro |
title | Effects of Electromagnetic Waves with LTE and 5G Bandwidth on the Skin Pigmentation In Vitro |
title_full | Effects of Electromagnetic Waves with LTE and 5G Bandwidth on the Skin Pigmentation In Vitro |
title_fullStr | Effects of Electromagnetic Waves with LTE and 5G Bandwidth on the Skin Pigmentation In Vitro |
title_full_unstemmed | Effects of Electromagnetic Waves with LTE and 5G Bandwidth on the Skin Pigmentation In Vitro |
title_short | Effects of Electromagnetic Waves with LTE and 5G Bandwidth on the Skin Pigmentation In Vitro |
title_sort | effects of electromagnetic waves with lte and 5g bandwidth on the skin pigmentation in vitro |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7794711/ https://www.ncbi.nlm.nih.gov/pubmed/33375304 http://dx.doi.org/10.3390/ijms22010170 |
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