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Transcriptional Homeostasis of Oxidative Stress-Related Pathways in Altered Gravity
Whereby several types of cultured cells are sensitive to gravity, the immune system belongs to the most affected systems during spaceflight. Since reactive oxygen species/reactive nitrogen species (ROS/RNS) are serving as signals of cellular homeostasis, particularly in the cells of the immune syste...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6164947/ https://www.ncbi.nlm.nih.gov/pubmed/30231541 http://dx.doi.org/10.3390/ijms19092814 |
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author | Tauber, Svantje Christoffel, Swantje Thiel, Cora Sandra Ullrich, Oliver |
author_facet | Tauber, Svantje Christoffel, Swantje Thiel, Cora Sandra Ullrich, Oliver |
author_sort | Tauber, Svantje |
collection | PubMed |
description | Whereby several types of cultured cells are sensitive to gravity, the immune system belongs to the most affected systems during spaceflight. Since reactive oxygen species/reactive nitrogen species (ROS/RNS) are serving as signals of cellular homeostasis, particularly in the cells of the immune system, we investigated the immediate effect of altered gravity on the transcription of 86 genes involved in reactive oxygen species metabolism, antioxidative systems, and cellular response to oxidative stress, using parabolic flight and suborbital ballistic rocket experiments and microarray analysis. In human myelomonocytic U937 cells, we detected a rapid response of 19.8% of all of the investigated oxidative stress-related transcripts to 1.8 g of hypergravity and 1.1% to microgravity as early as after 20 s. Nearly all (97.2%) of the initially altered transcripts adapted after 75 s of hypergravity (max. 13.5 g), and 100% adapted after 5 min of microgravity. After the almost complete adaptation of initially altered transcripts, a significant second pool of differentially expressed transcripts appeared. In contrast, we detected nearly no response of oxidative stress-related transcripts in human Jurkat T cells to altered gravity. In conclusion, we assume a very well-regulated homeostasis and transcriptional stability of oxidative stress-related pathways in altered gravity in cells of the human immune system. |
format | Online Article Text |
id | pubmed-6164947 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-61649472018-10-10 Transcriptional Homeostasis of Oxidative Stress-Related Pathways in Altered Gravity Tauber, Svantje Christoffel, Swantje Thiel, Cora Sandra Ullrich, Oliver Int J Mol Sci Article Whereby several types of cultured cells are sensitive to gravity, the immune system belongs to the most affected systems during spaceflight. Since reactive oxygen species/reactive nitrogen species (ROS/RNS) are serving as signals of cellular homeostasis, particularly in the cells of the immune system, we investigated the immediate effect of altered gravity on the transcription of 86 genes involved in reactive oxygen species metabolism, antioxidative systems, and cellular response to oxidative stress, using parabolic flight and suborbital ballistic rocket experiments and microarray analysis. In human myelomonocytic U937 cells, we detected a rapid response of 19.8% of all of the investigated oxidative stress-related transcripts to 1.8 g of hypergravity and 1.1% to microgravity as early as after 20 s. Nearly all (97.2%) of the initially altered transcripts adapted after 75 s of hypergravity (max. 13.5 g), and 100% adapted after 5 min of microgravity. After the almost complete adaptation of initially altered transcripts, a significant second pool of differentially expressed transcripts appeared. In contrast, we detected nearly no response of oxidative stress-related transcripts in human Jurkat T cells to altered gravity. In conclusion, we assume a very well-regulated homeostasis and transcriptional stability of oxidative stress-related pathways in altered gravity in cells of the human immune system. MDPI 2018-09-18 /pmc/articles/PMC6164947/ /pubmed/30231541 http://dx.doi.org/10.3390/ijms19092814 Text en © 2018 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 Tauber, Svantje Christoffel, Swantje Thiel, Cora Sandra Ullrich, Oliver Transcriptional Homeostasis of Oxidative Stress-Related Pathways in Altered Gravity |
title | Transcriptional Homeostasis of Oxidative Stress-Related Pathways in Altered Gravity |
title_full | Transcriptional Homeostasis of Oxidative Stress-Related Pathways in Altered Gravity |
title_fullStr | Transcriptional Homeostasis of Oxidative Stress-Related Pathways in Altered Gravity |
title_full_unstemmed | Transcriptional Homeostasis of Oxidative Stress-Related Pathways in Altered Gravity |
title_short | Transcriptional Homeostasis of Oxidative Stress-Related Pathways in Altered Gravity |
title_sort | transcriptional homeostasis of oxidative stress-related pathways in altered gravity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6164947/ https://www.ncbi.nlm.nih.gov/pubmed/30231541 http://dx.doi.org/10.3390/ijms19092814 |
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