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Tropoelastin-Pretreated Exosomes from Adipose-Derived Stem Cells Improve the Synthesis of Cartilage Matrix and Alleviate Osteoarthritis
Mesenchymal stem cells (MSCs) have recently been widely used to treat osteoarthritis (OA). Our prior research shows that tropoelastin (TE) increases MSC activity and protects knee cartilage from OA-related degradation. The underlying mechanism might be that TE regulates the paracrine of MSCs. Exosom...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10143921/ https://www.ncbi.nlm.nih.gov/pubmed/37103293 http://dx.doi.org/10.3390/jfb14040203 |
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author | Meng, Shuo Tang, Cong Deng, Muhai Yuan, Jie Fan, Yanli Gao, Shasha Feng, Yong Yang, Junjun Chen, Cheng |
author_facet | Meng, Shuo Tang, Cong Deng, Muhai Yuan, Jie Fan, Yanli Gao, Shasha Feng, Yong Yang, Junjun Chen, Cheng |
author_sort | Meng, Shuo |
collection | PubMed |
description | Mesenchymal stem cells (MSCs) have recently been widely used to treat osteoarthritis (OA). Our prior research shows that tropoelastin (TE) increases MSC activity and protects knee cartilage from OA-related degradation. The underlying mechanism might be that TE regulates the paracrine of MSCs. Exosomes (Exos), the paracrine secretion of MSCs, have been found to protect chondrocytes, reduce inflammation, and preserve the cartilage matrix. In this study, we used Exos derived from TE-pretreated adipose-derived stem cells (ADSCs) (TE-Exo(ADSCs)) as an injection medium, and compared it with Exos derived from unpretreated ADSCs (Exo(ADSCs)). We found that TE-Exo(ADSCs) could effectively enhance the matrix synthesis of chondrocytes in vitro. Moreover, TE pretreatment increased the ability of ADSCs to secrete Exos. In addition, compared with Exo(ADSCs), TE-Exo(ADSCs) exhibited therapeutic effects in the anterior cruciate ligament transection (ACLT)-induced OA model. Further, we observed that TE altered the microRNA expression in Exo(ADSCs) and identified one differentially upregulated microRNA: miR-451-5p. In conclusion, TE-Exo(ADSCs) helped maintain the chondrocyte phenotype in vitro, and promoted cartilage repair in vivo. These therapeutic effects might be related with the altered expression of miR-451-5p in the Exo(ADSCs). Thus, the intra-articular delivery of Exos derived from ADSCs with TE pretreatment could be a new approach to treat OA. |
format | Online Article Text |
id | pubmed-10143921 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-101439212023-04-29 Tropoelastin-Pretreated Exosomes from Adipose-Derived Stem Cells Improve the Synthesis of Cartilage Matrix and Alleviate Osteoarthritis Meng, Shuo Tang, Cong Deng, Muhai Yuan, Jie Fan, Yanli Gao, Shasha Feng, Yong Yang, Junjun Chen, Cheng J Funct Biomater Article Mesenchymal stem cells (MSCs) have recently been widely used to treat osteoarthritis (OA). Our prior research shows that tropoelastin (TE) increases MSC activity and protects knee cartilage from OA-related degradation. The underlying mechanism might be that TE regulates the paracrine of MSCs. Exosomes (Exos), the paracrine secretion of MSCs, have been found to protect chondrocytes, reduce inflammation, and preserve the cartilage matrix. In this study, we used Exos derived from TE-pretreated adipose-derived stem cells (ADSCs) (TE-Exo(ADSCs)) as an injection medium, and compared it with Exos derived from unpretreated ADSCs (Exo(ADSCs)). We found that TE-Exo(ADSCs) could effectively enhance the matrix synthesis of chondrocytes in vitro. Moreover, TE pretreatment increased the ability of ADSCs to secrete Exos. In addition, compared with Exo(ADSCs), TE-Exo(ADSCs) exhibited therapeutic effects in the anterior cruciate ligament transection (ACLT)-induced OA model. Further, we observed that TE altered the microRNA expression in Exo(ADSCs) and identified one differentially upregulated microRNA: miR-451-5p. In conclusion, TE-Exo(ADSCs) helped maintain the chondrocyte phenotype in vitro, and promoted cartilage repair in vivo. These therapeutic effects might be related with the altered expression of miR-451-5p in the Exo(ADSCs). Thus, the intra-articular delivery of Exos derived from ADSCs with TE pretreatment could be a new approach to treat OA. MDPI 2023-04-06 /pmc/articles/PMC10143921/ /pubmed/37103293 http://dx.doi.org/10.3390/jfb14040203 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Meng, Shuo Tang, Cong Deng, Muhai Yuan, Jie Fan, Yanli Gao, Shasha Feng, Yong Yang, Junjun Chen, Cheng Tropoelastin-Pretreated Exosomes from Adipose-Derived Stem Cells Improve the Synthesis of Cartilage Matrix and Alleviate Osteoarthritis |
title | Tropoelastin-Pretreated Exosomes from Adipose-Derived Stem Cells Improve the Synthesis of Cartilage Matrix and Alleviate Osteoarthritis |
title_full | Tropoelastin-Pretreated Exosomes from Adipose-Derived Stem Cells Improve the Synthesis of Cartilage Matrix and Alleviate Osteoarthritis |
title_fullStr | Tropoelastin-Pretreated Exosomes from Adipose-Derived Stem Cells Improve the Synthesis of Cartilage Matrix and Alleviate Osteoarthritis |
title_full_unstemmed | Tropoelastin-Pretreated Exosomes from Adipose-Derived Stem Cells Improve the Synthesis of Cartilage Matrix and Alleviate Osteoarthritis |
title_short | Tropoelastin-Pretreated Exosomes from Adipose-Derived Stem Cells Improve the Synthesis of Cartilage Matrix and Alleviate Osteoarthritis |
title_sort | tropoelastin-pretreated exosomes from adipose-derived stem cells improve the synthesis of cartilage matrix and alleviate osteoarthritis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10143921/ https://www.ncbi.nlm.nih.gov/pubmed/37103293 http://dx.doi.org/10.3390/jfb14040203 |
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