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Improved Wound Healing and Skin Regeneration Ability of 3,2′-Dihydroxyflavone-Treated Mesenchymal Stem Cell-Derived Extracellular Vesicles

Flavonoids enhance the self-renewal and differentiation potential of mesenchymal stem cells (MSCs) and have therapeutic activities, including regenerative, anti-oxidative, and anti-inflammatory effects. Recent studies have revealed that MSC-derived extracellular vesicles (MSC-EVs) have therapeutic e...

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Autores principales: Kim, Sehee, Shin, Yeokyung, Choi, Yujin, Lim, Kyung-Min, Jeong, Yeojin, Dayem, Ahmed Abdal, Lee, Yoonjoo, An, Jongyub, Song, Kwonwoo, Jang, Soo Bin, Cho, Ssang-Goo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10138514/
https://www.ncbi.nlm.nih.gov/pubmed/37108128
http://dx.doi.org/10.3390/ijms24086964
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author Kim, Sehee
Shin, Yeokyung
Choi, Yujin
Lim, Kyung-Min
Jeong, Yeojin
Dayem, Ahmed Abdal
Lee, Yoonjoo
An, Jongyub
Song, Kwonwoo
Jang, Soo Bin
Cho, Ssang-Goo
author_facet Kim, Sehee
Shin, Yeokyung
Choi, Yujin
Lim, Kyung-Min
Jeong, Yeojin
Dayem, Ahmed Abdal
Lee, Yoonjoo
An, Jongyub
Song, Kwonwoo
Jang, Soo Bin
Cho, Ssang-Goo
author_sort Kim, Sehee
collection PubMed
description Flavonoids enhance the self-renewal and differentiation potential of mesenchymal stem cells (MSCs) and have therapeutic activities, including regenerative, anti-oxidative, and anti-inflammatory effects. Recent studies have revealed that MSC-derived extracellular vesicles (MSC-EVs) have therapeutic effects on tissue regeneration and inflammation. To facilitate further research on the therapeutic potential of MSC-EVs derived from flavonoid-treated MSCs, we surveyed the production of EVs and their therapeutic applications in wound regeneration. MSCs treated with flavonoids enhanced EV production twofold compared with naïve MSCs. EVs produced by MSCs treated with flavonoids (Fla-EVs) displayed significant anti-inflammatory and wound-healing effects in vitro. The wound-healing capacity of EVs was mediated by the upregulation of mitogen-activated protein kinase kinase (MEK)/extracellular signal-regulated kinase (ERK) signaling. Interestingly, the protein level of p-ERK under inhibition of MEK signals was maintained in Fla-EV-treated fibroblasts, suggesting that Fla-EVs have a higher therapeutic potential than naïve MSC-EVs (Cont-EVs) in wound healing. Moreover, the in vivo wound closure effect of the Fla-EVs showed significant improvement compared with that of the flavonoid-only treatment group and the Cont-EVs. This study provides a strategy for the efficient production of EVs with superior therapeutic potential using flavonoids.
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spelling pubmed-101385142023-04-28 Improved Wound Healing and Skin Regeneration Ability of 3,2′-Dihydroxyflavone-Treated Mesenchymal Stem Cell-Derived Extracellular Vesicles Kim, Sehee Shin, Yeokyung Choi, Yujin Lim, Kyung-Min Jeong, Yeojin Dayem, Ahmed Abdal Lee, Yoonjoo An, Jongyub Song, Kwonwoo Jang, Soo Bin Cho, Ssang-Goo Int J Mol Sci Article Flavonoids enhance the self-renewal and differentiation potential of mesenchymal stem cells (MSCs) and have therapeutic activities, including regenerative, anti-oxidative, and anti-inflammatory effects. Recent studies have revealed that MSC-derived extracellular vesicles (MSC-EVs) have therapeutic effects on tissue regeneration and inflammation. To facilitate further research on the therapeutic potential of MSC-EVs derived from flavonoid-treated MSCs, we surveyed the production of EVs and their therapeutic applications in wound regeneration. MSCs treated with flavonoids enhanced EV production twofold compared with naïve MSCs. EVs produced by MSCs treated with flavonoids (Fla-EVs) displayed significant anti-inflammatory and wound-healing effects in vitro. The wound-healing capacity of EVs was mediated by the upregulation of mitogen-activated protein kinase kinase (MEK)/extracellular signal-regulated kinase (ERK) signaling. Interestingly, the protein level of p-ERK under inhibition of MEK signals was maintained in Fla-EV-treated fibroblasts, suggesting that Fla-EVs have a higher therapeutic potential than naïve MSC-EVs (Cont-EVs) in wound healing. Moreover, the in vivo wound closure effect of the Fla-EVs showed significant improvement compared with that of the flavonoid-only treatment group and the Cont-EVs. This study provides a strategy for the efficient production of EVs with superior therapeutic potential using flavonoids. MDPI 2023-04-09 /pmc/articles/PMC10138514/ /pubmed/37108128 http://dx.doi.org/10.3390/ijms24086964 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
Kim, Sehee
Shin, Yeokyung
Choi, Yujin
Lim, Kyung-Min
Jeong, Yeojin
Dayem, Ahmed Abdal
Lee, Yoonjoo
An, Jongyub
Song, Kwonwoo
Jang, Soo Bin
Cho, Ssang-Goo
Improved Wound Healing and Skin Regeneration Ability of 3,2′-Dihydroxyflavone-Treated Mesenchymal Stem Cell-Derived Extracellular Vesicles
title Improved Wound Healing and Skin Regeneration Ability of 3,2′-Dihydroxyflavone-Treated Mesenchymal Stem Cell-Derived Extracellular Vesicles
title_full Improved Wound Healing and Skin Regeneration Ability of 3,2′-Dihydroxyflavone-Treated Mesenchymal Stem Cell-Derived Extracellular Vesicles
title_fullStr Improved Wound Healing and Skin Regeneration Ability of 3,2′-Dihydroxyflavone-Treated Mesenchymal Stem Cell-Derived Extracellular Vesicles
title_full_unstemmed Improved Wound Healing and Skin Regeneration Ability of 3,2′-Dihydroxyflavone-Treated Mesenchymal Stem Cell-Derived Extracellular Vesicles
title_short Improved Wound Healing and Skin Regeneration Ability of 3,2′-Dihydroxyflavone-Treated Mesenchymal Stem Cell-Derived Extracellular Vesicles
title_sort improved wound healing and skin regeneration ability of 3,2′-dihydroxyflavone-treated mesenchymal stem cell-derived extracellular vesicles
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10138514/
https://www.ncbi.nlm.nih.gov/pubmed/37108128
http://dx.doi.org/10.3390/ijms24086964
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