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Signatures of muscle disuse in spaceflight and bed rest revealed by single muscle fiber proteomics
Astronauts experience dramatic loss of muscle mass, decreased strength, and insulin resistance, despite performing daily intense physical exercise that would lead to muscle growth on Earth. Partially mimicking spaceflight, prolonged bed rest causes muscle atrophy, loss of force, and glucose intolera...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9896895/ https://www.ncbi.nlm.nih.gov/pubmed/36741463 http://dx.doi.org/10.1093/pnasnexus/pgac086 |
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author | Murgia, Marta Ciciliot, Stefano Nagaraj, Nagarjuna Reggiani, Carlo Schiaffino, Stefano Franchi, Martino V Pišot, Rado Šimunič, Boštjan Toniolo, Luana Blaauw, Bert Sandri, Marco Biolo, Gianni Flück, Martin Narici, Marco V Mann, Matthias |
author_facet | Murgia, Marta Ciciliot, Stefano Nagaraj, Nagarjuna Reggiani, Carlo Schiaffino, Stefano Franchi, Martino V Pišot, Rado Šimunič, Boštjan Toniolo, Luana Blaauw, Bert Sandri, Marco Biolo, Gianni Flück, Martin Narici, Marco V Mann, Matthias |
author_sort | Murgia, Marta |
collection | PubMed |
description | Astronauts experience dramatic loss of muscle mass, decreased strength, and insulin resistance, despite performing daily intense physical exercise that would lead to muscle growth on Earth. Partially mimicking spaceflight, prolonged bed rest causes muscle atrophy, loss of force, and glucose intolerance. To unravel the underlying mechanisms, we employed highly sensitive single fiber proteomics to detail the molecular remodeling caused by unloading and inactivity during bed rest and changes of the muscle proteome of astronauts before and after a mission on the International Space Station. Muscle focal adhesions, involved in fiber–matrix interaction and insulin receptor stabilization, are prominently downregulated in both bed rest and spaceflight and restored upon reloading. Pathways of antioxidant response increased strongly in slow but not in fast muscle fibers. Unloading alone upregulated markers of neuromuscular damage and the pathway controlling EIF5A hypusination. These proteomic signatures of mechanical unloading in muscle fiber subtypes contribute to disentangle the effect of microgravity from the pleiotropic challenges of spaceflight. |
format | Online Article Text |
id | pubmed-9896895 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-98968952023-02-04 Signatures of muscle disuse in spaceflight and bed rest revealed by single muscle fiber proteomics Murgia, Marta Ciciliot, Stefano Nagaraj, Nagarjuna Reggiani, Carlo Schiaffino, Stefano Franchi, Martino V Pišot, Rado Šimunič, Boštjan Toniolo, Luana Blaauw, Bert Sandri, Marco Biolo, Gianni Flück, Martin Narici, Marco V Mann, Matthias PNAS Nexus Biological, Health, and Medical Sciences Astronauts experience dramatic loss of muscle mass, decreased strength, and insulin resistance, despite performing daily intense physical exercise that would lead to muscle growth on Earth. Partially mimicking spaceflight, prolonged bed rest causes muscle atrophy, loss of force, and glucose intolerance. To unravel the underlying mechanisms, we employed highly sensitive single fiber proteomics to detail the molecular remodeling caused by unloading and inactivity during bed rest and changes of the muscle proteome of astronauts before and after a mission on the International Space Station. Muscle focal adhesions, involved in fiber–matrix interaction and insulin receptor stabilization, are prominently downregulated in both bed rest and spaceflight and restored upon reloading. Pathways of antioxidant response increased strongly in slow but not in fast muscle fibers. Unloading alone upregulated markers of neuromuscular damage and the pathway controlling EIF5A hypusination. These proteomic signatures of mechanical unloading in muscle fiber subtypes contribute to disentangle the effect of microgravity from the pleiotropic challenges of spaceflight. Oxford University Press 2022-06-11 /pmc/articles/PMC9896895/ /pubmed/36741463 http://dx.doi.org/10.1093/pnasnexus/pgac086 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the National Academy of Sciences. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Biological, Health, and Medical Sciences Murgia, Marta Ciciliot, Stefano Nagaraj, Nagarjuna Reggiani, Carlo Schiaffino, Stefano Franchi, Martino V Pišot, Rado Šimunič, Boštjan Toniolo, Luana Blaauw, Bert Sandri, Marco Biolo, Gianni Flück, Martin Narici, Marco V Mann, Matthias Signatures of muscle disuse in spaceflight and bed rest revealed by single muscle fiber proteomics |
title | Signatures of muscle disuse in spaceflight and bed rest revealed by single muscle fiber proteomics |
title_full | Signatures of muscle disuse in spaceflight and bed rest revealed by single muscle fiber proteomics |
title_fullStr | Signatures of muscle disuse in spaceflight and bed rest revealed by single muscle fiber proteomics |
title_full_unstemmed | Signatures of muscle disuse in spaceflight and bed rest revealed by single muscle fiber proteomics |
title_short | Signatures of muscle disuse in spaceflight and bed rest revealed by single muscle fiber proteomics |
title_sort | signatures of muscle disuse in spaceflight and bed rest revealed by single muscle fiber proteomics |
topic | Biological, Health, and Medical Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9896895/ https://www.ncbi.nlm.nih.gov/pubmed/36741463 http://dx.doi.org/10.1093/pnasnexus/pgac086 |
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