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Meteorin-like is an injectable peptide that can enhance regeneration in aged muscle through immune-driven fibro/adipogenic progenitor signaling

Pathologies associated with sarcopenia include decline in muscular strength, lean mass and regenerative capacity. Despite the substantial impact on quality of life, no pharmacological therapeutics are available to counteract the age-associated decline in functional capacity and/or, resilience. Evide...

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Autores principales: Lee, David E., McKay, Lauren K., Bareja, Akshay, Li, Yongwu, Khodabukus, Alastair, Bursac, Nenad, Taylor, Gregory A., Baht, Gurpreet S., White, James P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9734561/
https://www.ncbi.nlm.nih.gov/pubmed/36494364
http://dx.doi.org/10.1038/s41467-022-35390-3
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author Lee, David E.
McKay, Lauren K.
Bareja, Akshay
Li, Yongwu
Khodabukus, Alastair
Bursac, Nenad
Taylor, Gregory A.
Baht, Gurpreet S.
White, James P.
author_facet Lee, David E.
McKay, Lauren K.
Bareja, Akshay
Li, Yongwu
Khodabukus, Alastair
Bursac, Nenad
Taylor, Gregory A.
Baht, Gurpreet S.
White, James P.
author_sort Lee, David E.
collection PubMed
description Pathologies associated with sarcopenia include decline in muscular strength, lean mass and regenerative capacity. Despite the substantial impact on quality of life, no pharmacological therapeutics are available to counteract the age-associated decline in functional capacity and/or, resilience. Evidence suggests immune-secreted cytokines can improve muscle regeneration, a strategy which we leverage in this study by rescuing the age-related deficiency in Meteorin-like through several in vivo add-back models. Notably, the intramuscular, peptide injection of recombinant METRNL was sufficient to improve muscle regeneration in aging. Using ex vivo media exchange and in vivo TNF inhibition, we demonstrate a mechanism of METRNL action during regeneration, showing it counteracts a pro-fibrotic gene program by triggering TNFα-induced apoptosis of fibro/adipogenic progenitor cells. These findings demonstrate therapeutic applications for METRNL to improve aged muscle, and show Fibro/Adipogenic Progenitors are viable therapeutic targets to counteract age-related loss in muscle resilience.
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spelling pubmed-97345612022-12-11 Meteorin-like is an injectable peptide that can enhance regeneration in aged muscle through immune-driven fibro/adipogenic progenitor signaling Lee, David E. McKay, Lauren K. Bareja, Akshay Li, Yongwu Khodabukus, Alastair Bursac, Nenad Taylor, Gregory A. Baht, Gurpreet S. White, James P. Nat Commun Article Pathologies associated with sarcopenia include decline in muscular strength, lean mass and regenerative capacity. Despite the substantial impact on quality of life, no pharmacological therapeutics are available to counteract the age-associated decline in functional capacity and/or, resilience. Evidence suggests immune-secreted cytokines can improve muscle regeneration, a strategy which we leverage in this study by rescuing the age-related deficiency in Meteorin-like through several in vivo add-back models. Notably, the intramuscular, peptide injection of recombinant METRNL was sufficient to improve muscle regeneration in aging. Using ex vivo media exchange and in vivo TNF inhibition, we demonstrate a mechanism of METRNL action during regeneration, showing it counteracts a pro-fibrotic gene program by triggering TNFα-induced apoptosis of fibro/adipogenic progenitor cells. These findings demonstrate therapeutic applications for METRNL to improve aged muscle, and show Fibro/Adipogenic Progenitors are viable therapeutic targets to counteract age-related loss in muscle resilience. Nature Publishing Group UK 2022-12-09 /pmc/articles/PMC9734561/ /pubmed/36494364 http://dx.doi.org/10.1038/s41467-022-35390-3 Text en © The Author(s) 2022 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
Lee, David E.
McKay, Lauren K.
Bareja, Akshay
Li, Yongwu
Khodabukus, Alastair
Bursac, Nenad
Taylor, Gregory A.
Baht, Gurpreet S.
White, James P.
Meteorin-like is an injectable peptide that can enhance regeneration in aged muscle through immune-driven fibro/adipogenic progenitor signaling
title Meteorin-like is an injectable peptide that can enhance regeneration in aged muscle through immune-driven fibro/adipogenic progenitor signaling
title_full Meteorin-like is an injectable peptide that can enhance regeneration in aged muscle through immune-driven fibro/adipogenic progenitor signaling
title_fullStr Meteorin-like is an injectable peptide that can enhance regeneration in aged muscle through immune-driven fibro/adipogenic progenitor signaling
title_full_unstemmed Meteorin-like is an injectable peptide that can enhance regeneration in aged muscle through immune-driven fibro/adipogenic progenitor signaling
title_short Meteorin-like is an injectable peptide that can enhance regeneration in aged muscle through immune-driven fibro/adipogenic progenitor signaling
title_sort meteorin-like is an injectable peptide that can enhance regeneration in aged muscle through immune-driven fibro/adipogenic progenitor signaling
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9734561/
https://www.ncbi.nlm.nih.gov/pubmed/36494364
http://dx.doi.org/10.1038/s41467-022-35390-3
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