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NAMPT encapsulated by extracellular vesicles from young adipose-derived mesenchymal stem cells treated tendinopathy in a “One-Stone-Two-Birds” manner

BACKGROUND: Tendinopathy is the leading sports-related injury and will cause severe weakness and tenderness. Effective therapy for tendinopathy remains limited, and extracellular vesicles (EVs) derived from adipose tissue-derived mesenchymal stem cells (ADMSCs) have demonstrated great potential in t...

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Autores principales: Wu, Guanghao, Su, Qihang, Li, Jie, Xue, Chao, Zhu, Jie, Cai, Qiuchen, Huang, Jingbiao, Ji, Shaoyang, Cheng, Biao, Ge, Hengan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9814467/
https://www.ncbi.nlm.nih.gov/pubmed/36604715
http://dx.doi.org/10.1186/s12951-022-01763-5
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author Wu, Guanghao
Su, Qihang
Li, Jie
Xue, Chao
Zhu, Jie
Cai, Qiuchen
Huang, Jingbiao
Ji, Shaoyang
Cheng, Biao
Ge, Hengan
author_facet Wu, Guanghao
Su, Qihang
Li, Jie
Xue, Chao
Zhu, Jie
Cai, Qiuchen
Huang, Jingbiao
Ji, Shaoyang
Cheng, Biao
Ge, Hengan
author_sort Wu, Guanghao
collection PubMed
description BACKGROUND: Tendinopathy is the leading sports-related injury and will cause severe weakness and tenderness. Effective therapy for tendinopathy remains limited, and extracellular vesicles (EVs) derived from adipose tissue-derived mesenchymal stem cells (ADMSCs) have demonstrated great potential in tendinopathy treatment; however, the influence of aging status on EV treatment has not been previously described. RESULTS: In this study, it was found that ADMSCs derived from old mice (ADMSC(old)) demonstrated remarkable cellular senescence and impaired NAD+ metabolism compared with ADMSCs derived from young mice (ADMSC(young)). Lower NAMPT contents were detected in both ADMSC(old) and its secreted EVs (ADMSC(old)-EVs). Advanced animal experiments demonstrated that ADMSC(young)-EVs, but not ADMSC(old)-EVs, alleviated the pathological structural, functional and biomechanical properties in tendinopathy mice. Mechanistic analyses demonstrated that ADMSC(young)-EVs improved cell viability and relieved cellular senescence of tenocytes through the NAMPT/SIRT1/PPARγ/PGC-1α pathway. ADMSC(young)-EVs, but not ADMSC(old)-EVs, promoted phagocytosis and M2 polarization in macrophages through the NAMPT/SIRT1/Nf-κb p65/NLRP3 pathway. The macrophage/tenocyte crosstalk in tendinopathy was influenced by ADMSC(young)-EV treatment and thus it demonstrated "One-Stone-Two-Birds" effects in tendinopathy treatment. CONCLUSIONS: This study demonstrates an effective novel therapy for tendinopathy and uncovers the influence of donor age on curative effects by clarifying the detailed biological mechanism. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-022-01763-5.
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spelling pubmed-98144672023-01-06 NAMPT encapsulated by extracellular vesicles from young adipose-derived mesenchymal stem cells treated tendinopathy in a “One-Stone-Two-Birds” manner Wu, Guanghao Su, Qihang Li, Jie Xue, Chao Zhu, Jie Cai, Qiuchen Huang, Jingbiao Ji, Shaoyang Cheng, Biao Ge, Hengan J Nanobiotechnology Research BACKGROUND: Tendinopathy is the leading sports-related injury and will cause severe weakness and tenderness. Effective therapy for tendinopathy remains limited, and extracellular vesicles (EVs) derived from adipose tissue-derived mesenchymal stem cells (ADMSCs) have demonstrated great potential in tendinopathy treatment; however, the influence of aging status on EV treatment has not been previously described. RESULTS: In this study, it was found that ADMSCs derived from old mice (ADMSC(old)) demonstrated remarkable cellular senescence and impaired NAD+ metabolism compared with ADMSCs derived from young mice (ADMSC(young)). Lower NAMPT contents were detected in both ADMSC(old) and its secreted EVs (ADMSC(old)-EVs). Advanced animal experiments demonstrated that ADMSC(young)-EVs, but not ADMSC(old)-EVs, alleviated the pathological structural, functional and biomechanical properties in tendinopathy mice. Mechanistic analyses demonstrated that ADMSC(young)-EVs improved cell viability and relieved cellular senescence of tenocytes through the NAMPT/SIRT1/PPARγ/PGC-1α pathway. ADMSC(young)-EVs, but not ADMSC(old)-EVs, promoted phagocytosis and M2 polarization in macrophages through the NAMPT/SIRT1/Nf-κb p65/NLRP3 pathway. The macrophage/tenocyte crosstalk in tendinopathy was influenced by ADMSC(young)-EV treatment and thus it demonstrated "One-Stone-Two-Birds" effects in tendinopathy treatment. CONCLUSIONS: This study demonstrates an effective novel therapy for tendinopathy and uncovers the influence of donor age on curative effects by clarifying the detailed biological mechanism. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-022-01763-5. BioMed Central 2023-01-05 /pmc/articles/PMC9814467/ /pubmed/36604715 http://dx.doi.org/10.1186/s12951-022-01763-5 Text en © The Author(s) 2023 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Wu, Guanghao
Su, Qihang
Li, Jie
Xue, Chao
Zhu, Jie
Cai, Qiuchen
Huang, Jingbiao
Ji, Shaoyang
Cheng, Biao
Ge, Hengan
NAMPT encapsulated by extracellular vesicles from young adipose-derived mesenchymal stem cells treated tendinopathy in a “One-Stone-Two-Birds” manner
title NAMPT encapsulated by extracellular vesicles from young adipose-derived mesenchymal stem cells treated tendinopathy in a “One-Stone-Two-Birds” manner
title_full NAMPT encapsulated by extracellular vesicles from young adipose-derived mesenchymal stem cells treated tendinopathy in a “One-Stone-Two-Birds” manner
title_fullStr NAMPT encapsulated by extracellular vesicles from young adipose-derived mesenchymal stem cells treated tendinopathy in a “One-Stone-Two-Birds” manner
title_full_unstemmed NAMPT encapsulated by extracellular vesicles from young adipose-derived mesenchymal stem cells treated tendinopathy in a “One-Stone-Two-Birds” manner
title_short NAMPT encapsulated by extracellular vesicles from young adipose-derived mesenchymal stem cells treated tendinopathy in a “One-Stone-Two-Birds” manner
title_sort nampt encapsulated by extracellular vesicles from young adipose-derived mesenchymal stem cells treated tendinopathy in a “one-stone-two-birds” manner
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9814467/
https://www.ncbi.nlm.nih.gov/pubmed/36604715
http://dx.doi.org/10.1186/s12951-022-01763-5
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