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Aging disrupts gene expression timing during muscle regeneration
Skeletal muscle function and regenerative capacity decline during aging, yet factors driving these changes are incompletely understood. Muscle regeneration requires temporally coordinated transcriptional programs to drive myogenic stem cells to activate, proliferate, fuse to form myofibers, and to m...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10277839/ https://www.ncbi.nlm.nih.gov/pubmed/37315524 http://dx.doi.org/10.1016/j.stemcr.2023.05.005 |
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author | Kurland, Jesse V. Cutler, Alicia A. Stanley, Jacob T. Betta, Nicole Dalla Van Deusen, Ashleigh Pawlikowski, Brad Hall, Monica Antwine, Tiffany Russell, Alan Allen, Mary Ann Dowell, Robin Olwin, Bradley |
author_facet | Kurland, Jesse V. Cutler, Alicia A. Stanley, Jacob T. Betta, Nicole Dalla Van Deusen, Ashleigh Pawlikowski, Brad Hall, Monica Antwine, Tiffany Russell, Alan Allen, Mary Ann Dowell, Robin Olwin, Bradley |
author_sort | Kurland, Jesse V. |
collection | PubMed |
description | Skeletal muscle function and regenerative capacity decline during aging, yet factors driving these changes are incompletely understood. Muscle regeneration requires temporally coordinated transcriptional programs to drive myogenic stem cells to activate, proliferate, fuse to form myofibers, and to mature as myonuclei, restoring muscle function after injury. We assessed global changes in myogenic transcription programs distinguishing muscle regeneration in aged mice from young mice by comparing pseudotime trajectories from single-nucleus RNA sequencing of myogenic nuclei. Aging-specific differences in coordinating myogenic transcription programs necessary for restoring muscle function occur following muscle injury, likely contributing to compromised regeneration in aged mice. Differences in pseudotime alignment of myogenic nuclei when comparing aged with young mice via dynamic time warping revealed pseudotemporal differences becoming progressively more severe as regeneration proceeds. Disruptions in timing of myogenic gene expression programs may contribute to incomplete skeletal muscle regeneration and declines in muscle function as organisms age. |
format | Online Article Text |
id | pubmed-10277839 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-102778392023-06-20 Aging disrupts gene expression timing during muscle regeneration Kurland, Jesse V. Cutler, Alicia A. Stanley, Jacob T. Betta, Nicole Dalla Van Deusen, Ashleigh Pawlikowski, Brad Hall, Monica Antwine, Tiffany Russell, Alan Allen, Mary Ann Dowell, Robin Olwin, Bradley Stem Cell Reports Article Skeletal muscle function and regenerative capacity decline during aging, yet factors driving these changes are incompletely understood. Muscle regeneration requires temporally coordinated transcriptional programs to drive myogenic stem cells to activate, proliferate, fuse to form myofibers, and to mature as myonuclei, restoring muscle function after injury. We assessed global changes in myogenic transcription programs distinguishing muscle regeneration in aged mice from young mice by comparing pseudotime trajectories from single-nucleus RNA sequencing of myogenic nuclei. Aging-specific differences in coordinating myogenic transcription programs necessary for restoring muscle function occur following muscle injury, likely contributing to compromised regeneration in aged mice. Differences in pseudotime alignment of myogenic nuclei when comparing aged with young mice via dynamic time warping revealed pseudotemporal differences becoming progressively more severe as regeneration proceeds. Disruptions in timing of myogenic gene expression programs may contribute to incomplete skeletal muscle regeneration and declines in muscle function as organisms age. Elsevier 2023-06-13 /pmc/articles/PMC10277839/ /pubmed/37315524 http://dx.doi.org/10.1016/j.stemcr.2023.05.005 Text en © 2023 The Author(s) https://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 Kurland, Jesse V. Cutler, Alicia A. Stanley, Jacob T. Betta, Nicole Dalla Van Deusen, Ashleigh Pawlikowski, Brad Hall, Monica Antwine, Tiffany Russell, Alan Allen, Mary Ann Dowell, Robin Olwin, Bradley Aging disrupts gene expression timing during muscle regeneration |
title | Aging disrupts gene expression timing during muscle regeneration |
title_full | Aging disrupts gene expression timing during muscle regeneration |
title_fullStr | Aging disrupts gene expression timing during muscle regeneration |
title_full_unstemmed | Aging disrupts gene expression timing during muscle regeneration |
title_short | Aging disrupts gene expression timing during muscle regeneration |
title_sort | aging disrupts gene expression timing during muscle regeneration |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10277839/ https://www.ncbi.nlm.nih.gov/pubmed/37315524 http://dx.doi.org/10.1016/j.stemcr.2023.05.005 |
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