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Clinical-grade human umbilical cord-derived mesenchymal stem cells improved skeletal muscle dysfunction in age-associated sarcopenia mice

With the expansion of the aging population, age-associated sarcopenia (AAS) has become a severe clinical disease of the elderly and a key challenge for healthy aging. Regrettably, no approved therapies currently exist for treating AAS. In this study, clinical-grade human umbilical cord-derived mesen...

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Autores principales: Wang, Chao, Zhao, Bichun, Zhai, Jinglei, Wang, Ailin, Cao, Ning, Liao, Tuling, Su, Ruyu, He, Lijuan, Li, Yanhua, Pei, Xuetao, Jia, Yali, Yue, Wen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10182022/
https://www.ncbi.nlm.nih.gov/pubmed/37173309
http://dx.doi.org/10.1038/s41419-023-05843-8
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author Wang, Chao
Zhao, Bichun
Zhai, Jinglei
Wang, Ailin
Cao, Ning
Liao, Tuling
Su, Ruyu
He, Lijuan
Li, Yanhua
Pei, Xuetao
Jia, Yali
Yue, Wen
author_facet Wang, Chao
Zhao, Bichun
Zhai, Jinglei
Wang, Ailin
Cao, Ning
Liao, Tuling
Su, Ruyu
He, Lijuan
Li, Yanhua
Pei, Xuetao
Jia, Yali
Yue, Wen
author_sort Wang, Chao
collection PubMed
description With the expansion of the aging population, age-associated sarcopenia (AAS) has become a severe clinical disease of the elderly and a key challenge for healthy aging. Regrettably, no approved therapies currently exist for treating AAS. In this study, clinical-grade human umbilical cord-derived mesenchymal stem cells (hUC-MSCs) were administrated to two classic mouse models (SAMP8 mice and D-galactose-induced aging mice), and their effects on skeletal muscle mass and function were investigated by behavioral tests, immunostaining, and western blotting. Core data results showed that hUC-MSCs significantly restored skeletal muscle strength and performance in both mouse models via mechanisms including raising the expression of crucial extracellular matrix proteins, activating satellite cells, enhancing autophagy, and impeding cellular aging. For the first time, the study comprehensively evaluates and demonstrates the preclinical efficacy of clinical-grade hUC-MSCs for AAS in two mouse models, which not only provides a novel model for AAS, but also highlights a promising strategy to improve and treat AAS and other age-associated muscle diseases. [Figure: see text]
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spelling pubmed-101820222023-05-14 Clinical-grade human umbilical cord-derived mesenchymal stem cells improved skeletal muscle dysfunction in age-associated sarcopenia mice Wang, Chao Zhao, Bichun Zhai, Jinglei Wang, Ailin Cao, Ning Liao, Tuling Su, Ruyu He, Lijuan Li, Yanhua Pei, Xuetao Jia, Yali Yue, Wen Cell Death Dis Article With the expansion of the aging population, age-associated sarcopenia (AAS) has become a severe clinical disease of the elderly and a key challenge for healthy aging. Regrettably, no approved therapies currently exist for treating AAS. In this study, clinical-grade human umbilical cord-derived mesenchymal stem cells (hUC-MSCs) were administrated to two classic mouse models (SAMP8 mice and D-galactose-induced aging mice), and their effects on skeletal muscle mass and function were investigated by behavioral tests, immunostaining, and western blotting. Core data results showed that hUC-MSCs significantly restored skeletal muscle strength and performance in both mouse models via mechanisms including raising the expression of crucial extracellular matrix proteins, activating satellite cells, enhancing autophagy, and impeding cellular aging. For the first time, the study comprehensively evaluates and demonstrates the preclinical efficacy of clinical-grade hUC-MSCs for AAS in two mouse models, which not only provides a novel model for AAS, but also highlights a promising strategy to improve and treat AAS and other age-associated muscle diseases. [Figure: see text] Nature Publishing Group UK 2023-05-12 /pmc/articles/PMC10182022/ /pubmed/37173309 http://dx.doi.org/10.1038/s41419-023-05843-8 Text en © The Author(s) 2023 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
Wang, Chao
Zhao, Bichun
Zhai, Jinglei
Wang, Ailin
Cao, Ning
Liao, Tuling
Su, Ruyu
He, Lijuan
Li, Yanhua
Pei, Xuetao
Jia, Yali
Yue, Wen
Clinical-grade human umbilical cord-derived mesenchymal stem cells improved skeletal muscle dysfunction in age-associated sarcopenia mice
title Clinical-grade human umbilical cord-derived mesenchymal stem cells improved skeletal muscle dysfunction in age-associated sarcopenia mice
title_full Clinical-grade human umbilical cord-derived mesenchymal stem cells improved skeletal muscle dysfunction in age-associated sarcopenia mice
title_fullStr Clinical-grade human umbilical cord-derived mesenchymal stem cells improved skeletal muscle dysfunction in age-associated sarcopenia mice
title_full_unstemmed Clinical-grade human umbilical cord-derived mesenchymal stem cells improved skeletal muscle dysfunction in age-associated sarcopenia mice
title_short Clinical-grade human umbilical cord-derived mesenchymal stem cells improved skeletal muscle dysfunction in age-associated sarcopenia mice
title_sort clinical-grade human umbilical cord-derived mesenchymal stem cells improved skeletal muscle dysfunction in age-associated sarcopenia mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10182022/
https://www.ncbi.nlm.nih.gov/pubmed/37173309
http://dx.doi.org/10.1038/s41419-023-05843-8
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