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Beyond Low-Earth Orbit: Characterizing Immune and microRNA Differentials following Simulated Deep Spaceflight Conditions in Mice

Spaceflight missions can cause immune system dysfunction in astronauts with little understanding of immune outcomes in deep space. This study assessed immune responses in mice following ground-based, simulated deep spaceflight conditions, compared with data from astronauts on International Space Sta...

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Autores principales: Paul, Amber M., Cheng-Campbell, Margareth, Blaber, Elizabeth A., Anand, Sulekha, Bhattacharya, Sharmila, Zwart, Sara R., Crucian, Brian E., Smith, Scott M., Meller, Robert, Grabham, Peter, Beheshti, Afshin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7756144/
https://www.ncbi.nlm.nih.gov/pubmed/33376970
http://dx.doi.org/10.1016/j.isci.2020.101747
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author Paul, Amber M.
Cheng-Campbell, Margareth
Blaber, Elizabeth A.
Anand, Sulekha
Bhattacharya, Sharmila
Zwart, Sara R.
Crucian, Brian E.
Smith, Scott M.
Meller, Robert
Grabham, Peter
Beheshti, Afshin
author_facet Paul, Amber M.
Cheng-Campbell, Margareth
Blaber, Elizabeth A.
Anand, Sulekha
Bhattacharya, Sharmila
Zwart, Sara R.
Crucian, Brian E.
Smith, Scott M.
Meller, Robert
Grabham, Peter
Beheshti, Afshin
author_sort Paul, Amber M.
collection PubMed
description Spaceflight missions can cause immune system dysfunction in astronauts with little understanding of immune outcomes in deep space. This study assessed immune responses in mice following ground-based, simulated deep spaceflight conditions, compared with data from astronauts on International Space Station missions. For ground studies, we simulated microgravity using the hindlimb unloaded mouse model alone or in combination with acute simulated galactic cosmic rays or solar particle events irradiation. Immune profiling results revealed unique immune diversity following each experimental condition, suggesting each stressor results in distinct circulating immune responses, with clear consequences for deep spaceflight. Circulating plasma microRNA sequence analysis revealed involvement in immune system dysregulation. Furthermore, a large astronaut cohort showed elevated inflammation during low-Earth orbit missions, thereby supporting our simulated ground experiments in mice. Herein, circulating immune biomarkers are defined by distinct deep space irradiation types coupled to simulated microgravity and could be targets for future space health initiatives.
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spelling pubmed-77561442020-12-28 Beyond Low-Earth Orbit: Characterizing Immune and microRNA Differentials following Simulated Deep Spaceflight Conditions in Mice Paul, Amber M. Cheng-Campbell, Margareth Blaber, Elizabeth A. Anand, Sulekha Bhattacharya, Sharmila Zwart, Sara R. Crucian, Brian E. Smith, Scott M. Meller, Robert Grabham, Peter Beheshti, Afshin iScience Article Spaceflight missions can cause immune system dysfunction in astronauts with little understanding of immune outcomes in deep space. This study assessed immune responses in mice following ground-based, simulated deep spaceflight conditions, compared with data from astronauts on International Space Station missions. For ground studies, we simulated microgravity using the hindlimb unloaded mouse model alone or in combination with acute simulated galactic cosmic rays or solar particle events irradiation. Immune profiling results revealed unique immune diversity following each experimental condition, suggesting each stressor results in distinct circulating immune responses, with clear consequences for deep spaceflight. Circulating plasma microRNA sequence analysis revealed involvement in immune system dysregulation. Furthermore, a large astronaut cohort showed elevated inflammation during low-Earth orbit missions, thereby supporting our simulated ground experiments in mice. Herein, circulating immune biomarkers are defined by distinct deep space irradiation types coupled to simulated microgravity and could be targets for future space health initiatives. Elsevier 2020-11-25 /pmc/articles/PMC7756144/ /pubmed/33376970 http://dx.doi.org/10.1016/j.isci.2020.101747 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Paul, Amber M.
Cheng-Campbell, Margareth
Blaber, Elizabeth A.
Anand, Sulekha
Bhattacharya, Sharmila
Zwart, Sara R.
Crucian, Brian E.
Smith, Scott M.
Meller, Robert
Grabham, Peter
Beheshti, Afshin
Beyond Low-Earth Orbit: Characterizing Immune and microRNA Differentials following Simulated Deep Spaceflight Conditions in Mice
title Beyond Low-Earth Orbit: Characterizing Immune and microRNA Differentials following Simulated Deep Spaceflight Conditions in Mice
title_full Beyond Low-Earth Orbit: Characterizing Immune and microRNA Differentials following Simulated Deep Spaceflight Conditions in Mice
title_fullStr Beyond Low-Earth Orbit: Characterizing Immune and microRNA Differentials following Simulated Deep Spaceflight Conditions in Mice
title_full_unstemmed Beyond Low-Earth Orbit: Characterizing Immune and microRNA Differentials following Simulated Deep Spaceflight Conditions in Mice
title_short Beyond Low-Earth Orbit: Characterizing Immune and microRNA Differentials following Simulated Deep Spaceflight Conditions in Mice
title_sort beyond low-earth orbit: characterizing immune and microrna differentials following simulated deep spaceflight conditions in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7756144/
https://www.ncbi.nlm.nih.gov/pubmed/33376970
http://dx.doi.org/10.1016/j.isci.2020.101747
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