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Cytokine-primed umbilical cord mesenchymal stem cells enhanced therapeutic effects of extracellular vesicles on osteoarthritic chondrocytes
In recent years, extracellular vesicles (EVs) secreted by mesenchymal stem cells (MSCs) have emerged as a potential cell-free therapy against osteoarthritis (OA). Thus, we investigated the therapeutic effects of EVs released by cytokine-primed umbilical cord-derived MSCs (UCMSCs) on osteoarthritic c...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9647019/ https://www.ncbi.nlm.nih.gov/pubmed/36389838 http://dx.doi.org/10.3389/fimmu.2022.1041592 |
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author | Nguyen, Thu Huyen Dao, Huy Hoang Duong, Chau Minh Nguyen, Xuan-Hung Hoang, Diem Huong Do, Xuan-Hai Truong, Trung Quang Nguyen, Tu Dac Nguyen, Liem Thanh Than, Uyen Thi Trang |
author_facet | Nguyen, Thu Huyen Dao, Huy Hoang Duong, Chau Minh Nguyen, Xuan-Hung Hoang, Diem Huong Do, Xuan-Hai Truong, Trung Quang Nguyen, Tu Dac Nguyen, Liem Thanh Than, Uyen Thi Trang |
author_sort | Nguyen, Thu Huyen |
collection | PubMed |
description | In recent years, extracellular vesicles (EVs) secreted by mesenchymal stem cells (MSCs) have emerged as a potential cell-free therapy against osteoarthritis (OA). Thus, we investigated the therapeutic effects of EVs released by cytokine-primed umbilical cord-derived MSCs (UCMSCs) on osteoarthritic chondrocyte physiology. Priming UCMSCs individually with transforming growth factor beta (TGFβ), interferon alpha (IFNα), or tumor necrosis factor alpha (TNFα) significantly reduced the sorting of miR-181b-3p but not miR-320a-3p; two negative regulators of chondrocyte regeneration, into EVs. However, the EV treatment did not show any significant effect on chondrocyte proliferation. Meanwhile, EVs from both non-priming and cytokine-primed UCMSCs induced migration at later time points of measurement. Moreover, TGFβ-primed UCMSCs secreted EVs that could upregulate the expression of chondrogenesis markers (COL2 and ACAN) and downregulate fibrotic markers (COL1 and RUNX2) in chondrocytes. Hence, priming UCMSCs with cytokines can deliver selective therapeutic effects of EV treatment in OA and chondrocyte-related disorders. |
format | Online Article Text |
id | pubmed-9647019 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-96470192022-11-15 Cytokine-primed umbilical cord mesenchymal stem cells enhanced therapeutic effects of extracellular vesicles on osteoarthritic chondrocytes Nguyen, Thu Huyen Dao, Huy Hoang Duong, Chau Minh Nguyen, Xuan-Hung Hoang, Diem Huong Do, Xuan-Hai Truong, Trung Quang Nguyen, Tu Dac Nguyen, Liem Thanh Than, Uyen Thi Trang Front Immunol Immunology In recent years, extracellular vesicles (EVs) secreted by mesenchymal stem cells (MSCs) have emerged as a potential cell-free therapy against osteoarthritis (OA). Thus, we investigated the therapeutic effects of EVs released by cytokine-primed umbilical cord-derived MSCs (UCMSCs) on osteoarthritic chondrocyte physiology. Priming UCMSCs individually with transforming growth factor beta (TGFβ), interferon alpha (IFNα), or tumor necrosis factor alpha (TNFα) significantly reduced the sorting of miR-181b-3p but not miR-320a-3p; two negative regulators of chondrocyte regeneration, into EVs. However, the EV treatment did not show any significant effect on chondrocyte proliferation. Meanwhile, EVs from both non-priming and cytokine-primed UCMSCs induced migration at later time points of measurement. Moreover, TGFβ-primed UCMSCs secreted EVs that could upregulate the expression of chondrogenesis markers (COL2 and ACAN) and downregulate fibrotic markers (COL1 and RUNX2) in chondrocytes. Hence, priming UCMSCs with cytokines can deliver selective therapeutic effects of EV treatment in OA and chondrocyte-related disorders. Frontiers Media S.A. 2022-10-27 /pmc/articles/PMC9647019/ /pubmed/36389838 http://dx.doi.org/10.3389/fimmu.2022.1041592 Text en Copyright © 2022 Nguyen, Dao, Duong, Nguyen, Hoang, Do, Truong, Nguyen, Nguyen and Than https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Nguyen, Thu Huyen Dao, Huy Hoang Duong, Chau Minh Nguyen, Xuan-Hung Hoang, Diem Huong Do, Xuan-Hai Truong, Trung Quang Nguyen, Tu Dac Nguyen, Liem Thanh Than, Uyen Thi Trang Cytokine-primed umbilical cord mesenchymal stem cells enhanced therapeutic effects of extracellular vesicles on osteoarthritic chondrocytes |
title | Cytokine-primed umbilical cord mesenchymal stem cells enhanced therapeutic effects of extracellular vesicles on osteoarthritic chondrocytes |
title_full | Cytokine-primed umbilical cord mesenchymal stem cells enhanced therapeutic effects of extracellular vesicles on osteoarthritic chondrocytes |
title_fullStr | Cytokine-primed umbilical cord mesenchymal stem cells enhanced therapeutic effects of extracellular vesicles on osteoarthritic chondrocytes |
title_full_unstemmed | Cytokine-primed umbilical cord mesenchymal stem cells enhanced therapeutic effects of extracellular vesicles on osteoarthritic chondrocytes |
title_short | Cytokine-primed umbilical cord mesenchymal stem cells enhanced therapeutic effects of extracellular vesicles on osteoarthritic chondrocytes |
title_sort | cytokine-primed umbilical cord mesenchymal stem cells enhanced therapeutic effects of extracellular vesicles on osteoarthritic chondrocytes |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9647019/ https://www.ncbi.nlm.nih.gov/pubmed/36389838 http://dx.doi.org/10.3389/fimmu.2022.1041592 |
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