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Impacts of radiation exposure, hindlimb unloading, and recovery on murine skeletal muscle cell telomere length

Astronauts are exposed to harsh conditions, including cosmic radiation and microgravity. Spaceflight elongates human telomeres in peripheral blood, which shorten upon return to Earth and approach baseline levels during postflight recovery. Astronauts also encounter muscle atrophy, losing up to 20% l...

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Autores principales: Tichy, Elisia D., Lee, Ji-Hyung, Li, Grant, Estep, Katrina N., Brad Johnson, F., Mourkioti, Foteini
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10504369/
https://www.ncbi.nlm.nih.gov/pubmed/37714858
http://dx.doi.org/10.1038/s41526-023-00303-1
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author Tichy, Elisia D.
Lee, Ji-Hyung
Li, Grant
Estep, Katrina N.
Brad Johnson, F.
Mourkioti, Foteini
author_facet Tichy, Elisia D.
Lee, Ji-Hyung
Li, Grant
Estep, Katrina N.
Brad Johnson, F.
Mourkioti, Foteini
author_sort Tichy, Elisia D.
collection PubMed
description Astronauts are exposed to harsh conditions, including cosmic radiation and microgravity. Spaceflight elongates human telomeres in peripheral blood, which shorten upon return to Earth and approach baseline levels during postflight recovery. Astronauts also encounter muscle atrophy, losing up to 20% loss of muscle mass on spaceflights. Telomere length changes in muscle cells of astronauts remain unexplored. This study investigates telomere alterations in grounded mice experiencing radiation exposure and muscle atrophy, via a hindlimb unloading spaceflight mimicking model. We find telomere lengthening is present in muscle stem cells and in myofiber nuclei, but not in muscle-resident endothelial cells. We further assessed telomere length in the model following hindlimb unloading recovery. We find that telomere length failed to return to baseline values. Our results suggest a role for telomeres in muscle acclimatization, which is relevant for the well-being of astronauts in space, and upon their return to Earth.
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spelling pubmed-105043692023-09-17 Impacts of radiation exposure, hindlimb unloading, and recovery on murine skeletal muscle cell telomere length Tichy, Elisia D. Lee, Ji-Hyung Li, Grant Estep, Katrina N. Brad Johnson, F. Mourkioti, Foteini NPJ Microgravity Article Astronauts are exposed to harsh conditions, including cosmic radiation and microgravity. Spaceflight elongates human telomeres in peripheral blood, which shorten upon return to Earth and approach baseline levels during postflight recovery. Astronauts also encounter muscle atrophy, losing up to 20% loss of muscle mass on spaceflights. Telomere length changes in muscle cells of astronauts remain unexplored. This study investigates telomere alterations in grounded mice experiencing radiation exposure and muscle atrophy, via a hindlimb unloading spaceflight mimicking model. We find telomere lengthening is present in muscle stem cells and in myofiber nuclei, but not in muscle-resident endothelial cells. We further assessed telomere length in the model following hindlimb unloading recovery. We find that telomere length failed to return to baseline values. Our results suggest a role for telomeres in muscle acclimatization, which is relevant for the well-being of astronauts in space, and upon their return to Earth. Nature Publishing Group UK 2023-09-15 /pmc/articles/PMC10504369/ /pubmed/37714858 http://dx.doi.org/10.1038/s41526-023-00303-1 Text en © The Author(s) 2023 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
Tichy, Elisia D.
Lee, Ji-Hyung
Li, Grant
Estep, Katrina N.
Brad Johnson, F.
Mourkioti, Foteini
Impacts of radiation exposure, hindlimb unloading, and recovery on murine skeletal muscle cell telomere length
title Impacts of radiation exposure, hindlimb unloading, and recovery on murine skeletal muscle cell telomere length
title_full Impacts of radiation exposure, hindlimb unloading, and recovery on murine skeletal muscle cell telomere length
title_fullStr Impacts of radiation exposure, hindlimb unloading, and recovery on murine skeletal muscle cell telomere length
title_full_unstemmed Impacts of radiation exposure, hindlimb unloading, and recovery on murine skeletal muscle cell telomere length
title_short Impacts of radiation exposure, hindlimb unloading, and recovery on murine skeletal muscle cell telomere length
title_sort impacts of radiation exposure, hindlimb unloading, and recovery on murine skeletal muscle cell telomere length
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10504369/
https://www.ncbi.nlm.nih.gov/pubmed/37714858
http://dx.doi.org/10.1038/s41526-023-00303-1
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