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Elamipretide effects on the skeletal muscle phosphoproteome in aged female mice
The age-related decline in skeletal muscle mass and function is known as sarcopenia. Sarcopenia progresses based on complex processes involving protein dynamics, cell signaling, oxidative stress, and repair. We have previously found that 8-week treatment with elamipretide improves skeletal muscle fu...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9768078/ https://www.ncbi.nlm.nih.gov/pubmed/36322234 http://dx.doi.org/10.1007/s11357-022-00679-0 |
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author | Campbell, Matthew D. Martín-Pérez, Miguel Egertson, Jarrett D. Gaffrey, Matthew J. Wang, Lu Bammler, Theo Rabinovitch, Peter S. MacCoss, Michael Qian, Wei-Jun Villen, Judit Marcinek, David |
author_facet | Campbell, Matthew D. Martín-Pérez, Miguel Egertson, Jarrett D. Gaffrey, Matthew J. Wang, Lu Bammler, Theo Rabinovitch, Peter S. MacCoss, Michael Qian, Wei-Jun Villen, Judit Marcinek, David |
author_sort | Campbell, Matthew D. |
collection | PubMed |
description | The age-related decline in skeletal muscle mass and function is known as sarcopenia. Sarcopenia progresses based on complex processes involving protein dynamics, cell signaling, oxidative stress, and repair. We have previously found that 8-week treatment with elamipretide improves skeletal muscle function, reverses redox stress, and restores protein S-glutathionylation changes in aged female mice. This study tested whether 8-week treatment with elamipretide also affects global phosphorylation in skeletal muscle consistent with functional improvements and S-glutathionylation. Using female 6–7-month-old mice and 28–29-month-old mice, we found that phosphorylation changes did not relate to S-glutathionylation modifications, but that treatment with elamipretide did partially reverse age-related changes in protein phosphorylation in mouse skeletal muscle. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11357-022-00679-0. |
format | Online Article Text |
id | pubmed-9768078 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-97680782022-12-22 Elamipretide effects on the skeletal muscle phosphoproteome in aged female mice Campbell, Matthew D. Martín-Pérez, Miguel Egertson, Jarrett D. Gaffrey, Matthew J. Wang, Lu Bammler, Theo Rabinovitch, Peter S. MacCoss, Michael Qian, Wei-Jun Villen, Judit Marcinek, David GeroScience Original Article The age-related decline in skeletal muscle mass and function is known as sarcopenia. Sarcopenia progresses based on complex processes involving protein dynamics, cell signaling, oxidative stress, and repair. We have previously found that 8-week treatment with elamipretide improves skeletal muscle function, reverses redox stress, and restores protein S-glutathionylation changes in aged female mice. This study tested whether 8-week treatment with elamipretide also affects global phosphorylation in skeletal muscle consistent with functional improvements and S-glutathionylation. Using female 6–7-month-old mice and 28–29-month-old mice, we found that phosphorylation changes did not relate to S-glutathionylation modifications, but that treatment with elamipretide did partially reverse age-related changes in protein phosphorylation in mouse skeletal muscle. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11357-022-00679-0. Springer International Publishing 2022-11-02 /pmc/articles/PMC9768078/ /pubmed/36322234 http://dx.doi.org/10.1007/s11357-022-00679-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Campbell, Matthew D. Martín-Pérez, Miguel Egertson, Jarrett D. Gaffrey, Matthew J. Wang, Lu Bammler, Theo Rabinovitch, Peter S. MacCoss, Michael Qian, Wei-Jun Villen, Judit Marcinek, David Elamipretide effects on the skeletal muscle phosphoproteome in aged female mice |
title | Elamipretide effects on the skeletal muscle phosphoproteome in aged female mice |
title_full | Elamipretide effects on the skeletal muscle phosphoproteome in aged female mice |
title_fullStr | Elamipretide effects on the skeletal muscle phosphoproteome in aged female mice |
title_full_unstemmed | Elamipretide effects on the skeletal muscle phosphoproteome in aged female mice |
title_short | Elamipretide effects on the skeletal muscle phosphoproteome in aged female mice |
title_sort | elamipretide effects on the skeletal muscle phosphoproteome in aged female mice |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9768078/ https://www.ncbi.nlm.nih.gov/pubmed/36322234 http://dx.doi.org/10.1007/s11357-022-00679-0 |
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