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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...

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Autores principales: Tauber, Svantje, Christoffel, Swantje, Thiel, Cora Sandra, Ullrich, Oliver
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
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.
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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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