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3D cell culture using a clinostat reproduces microgravity-induced skin changes
Exposure to microgravity affects human physiology in various ways, and astronauts frequently report skin-related problems. Skin rash and irritation are frequent complaints during space missions, and skin thinning has also been reported after returning to Earth. However, spaceflight missions for stud...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8169764/ https://www.ncbi.nlm.nih.gov/pubmed/34075058 http://dx.doi.org/10.1038/s41526-021-00148-6 |
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author | Choi, Dong Hyun Jeon, Byoungjun Lim, Min Hyuk Lee, Dong Hun Ye, Sang-Kyu Jeong, Seung-Yong Kim, Sungwan |
author_facet | Choi, Dong Hyun Jeon, Byoungjun Lim, Min Hyuk Lee, Dong Hun Ye, Sang-Kyu Jeong, Seung-Yong Kim, Sungwan |
author_sort | Choi, Dong Hyun |
collection | PubMed |
description | Exposure to microgravity affects human physiology in various ways, and astronauts frequently report skin-related problems. Skin rash and irritation are frequent complaints during space missions, and skin thinning has also been reported after returning to Earth. However, spaceflight missions for studying the physiological changes in microgravity are impractical. Thus, we used a previously developed 3D clinostat to simulate a microgravity environment and investigate whether physiological changes of the skin can be reproduced in a 3D in vitro setting. Our results showed that under time-averaged simulated microgravity (taSMG), the thickness of the endothelial cell arrangement increased by up to 59.75%, indicating skin irritation due to vasodilation, and that the diameter of keratinocytes and fibroblast co-cultured spheroids decreased by 6.66%, representing skin thinning. The α1 chain of type I collagen was upregulated, while the connective tissue growth factor was downregulated under taSMG. Cytokeratin-10 expression was significantly increased in the taSMG environment. The clinostat-based 3D culture system can reproduce physiological changes in the skin similar to those under microgravity, providing insight for understanding the effects of microgravity on human health before space exploration. |
format | Online Article Text |
id | pubmed-8169764 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81697642021-06-07 3D cell culture using a clinostat reproduces microgravity-induced skin changes Choi, Dong Hyun Jeon, Byoungjun Lim, Min Hyuk Lee, Dong Hun Ye, Sang-Kyu Jeong, Seung-Yong Kim, Sungwan NPJ Microgravity Article Exposure to microgravity affects human physiology in various ways, and astronauts frequently report skin-related problems. Skin rash and irritation are frequent complaints during space missions, and skin thinning has also been reported after returning to Earth. However, spaceflight missions for studying the physiological changes in microgravity are impractical. Thus, we used a previously developed 3D clinostat to simulate a microgravity environment and investigate whether physiological changes of the skin can be reproduced in a 3D in vitro setting. Our results showed that under time-averaged simulated microgravity (taSMG), the thickness of the endothelial cell arrangement increased by up to 59.75%, indicating skin irritation due to vasodilation, and that the diameter of keratinocytes and fibroblast co-cultured spheroids decreased by 6.66%, representing skin thinning. The α1 chain of type I collagen was upregulated, while the connective tissue growth factor was downregulated under taSMG. Cytokeratin-10 expression was significantly increased in the taSMG environment. The clinostat-based 3D culture system can reproduce physiological changes in the skin similar to those under microgravity, providing insight for understanding the effects of microgravity on human health before space exploration. Nature Publishing Group UK 2021-06-01 /pmc/articles/PMC8169764/ /pubmed/34075058 http://dx.doi.org/10.1038/s41526-021-00148-6 Text en © The Author(s) 2021 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Choi, Dong Hyun Jeon, Byoungjun Lim, Min Hyuk Lee, Dong Hun Ye, Sang-Kyu Jeong, Seung-Yong Kim, Sungwan 3D cell culture using a clinostat reproduces microgravity-induced skin changes |
title | 3D cell culture using a clinostat reproduces microgravity-induced skin changes |
title_full | 3D cell culture using a clinostat reproduces microgravity-induced skin changes |
title_fullStr | 3D cell culture using a clinostat reproduces microgravity-induced skin changes |
title_full_unstemmed | 3D cell culture using a clinostat reproduces microgravity-induced skin changes |
title_short | 3D cell culture using a clinostat reproduces microgravity-induced skin changes |
title_sort | 3d cell culture using a clinostat reproduces microgravity-induced skin changes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8169764/ https://www.ncbi.nlm.nih.gov/pubmed/34075058 http://dx.doi.org/10.1038/s41526-021-00148-6 |
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