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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
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.
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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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