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TNF-α and INF-γ primed canine stem cell-derived extracellular vesicles alleviate experimental murine colitis

The inflammatory bowel diseases (IBD) are characterized by relapsing inflammation and immune activation diseases of the gastrointestinal tract. Extracellular vesicles, which elicit similar biological activity to the stem cell themselves, have been used experimentally to treat dextran sulfate sodium...

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Autores principales: An, Ju-Hyun, Li, Qiang, Bhang, Dong-Ha, Song, Woo-Jin, Youn, Hwa-Young
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7005871/
https://www.ncbi.nlm.nih.gov/pubmed/32034203
http://dx.doi.org/10.1038/s41598-020-58909-4
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author An, Ju-Hyun
Li, Qiang
Bhang, Dong-Ha
Song, Woo-Jin
Youn, Hwa-Young
author_facet An, Ju-Hyun
Li, Qiang
Bhang, Dong-Ha
Song, Woo-Jin
Youn, Hwa-Young
author_sort An, Ju-Hyun
collection PubMed
description The inflammatory bowel diseases (IBD) are characterized by relapsing inflammation and immune activation diseases of the gastrointestinal tract. Extracellular vesicles, which elicit similar biological activity to the stem cell themselves, have been used experimentally to treat dextran sulfate sodium (DSS)-induced colitis in murine models though immunosuppressive potential. In this study, we investigated whether the Extracellular vesicles (EVs) obtained by stimulating inflammatory cytokine on canine adipose mesenchymal stem cells (cASC) improved anti-inflammatory and/or immunosuppressive potential of EVs, and/or their ability to alleviate inflammation in colitis. We also explored the correlation between immune cells and the inflammatory repressive effect of primed EVs. Pro-inflammatory cytokines such as TNF-α and IFN-γ increased immunosuppressive protein such as HGF, TSG-6, PGE2 and TGF-β in EVs. Moreover, the anti-inflammatory effect of EVs was improved through pretreatment with inflammatory cytokines. Importantly, EVs obtained from primed stem cells effectively induced macrophage polarization toward an anti-inflammatory M2 phenotype and suppressed activated immunity by enhancing regulatory T cells in inflamed colon in mice. Our results provide a new and effective therapy for the EVs obtained from ASC stimulated with TNF-α and IFN-γ against not only IBD, but also immune-mediated disease.
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spelling pubmed-70058712020-02-18 TNF-α and INF-γ primed canine stem cell-derived extracellular vesicles alleviate experimental murine colitis An, Ju-Hyun Li, Qiang Bhang, Dong-Ha Song, Woo-Jin Youn, Hwa-Young Sci Rep Article The inflammatory bowel diseases (IBD) are characterized by relapsing inflammation and immune activation diseases of the gastrointestinal tract. Extracellular vesicles, which elicit similar biological activity to the stem cell themselves, have been used experimentally to treat dextran sulfate sodium (DSS)-induced colitis in murine models though immunosuppressive potential. In this study, we investigated whether the Extracellular vesicles (EVs) obtained by stimulating inflammatory cytokine on canine adipose mesenchymal stem cells (cASC) improved anti-inflammatory and/or immunosuppressive potential of EVs, and/or their ability to alleviate inflammation in colitis. We also explored the correlation between immune cells and the inflammatory repressive effect of primed EVs. Pro-inflammatory cytokines such as TNF-α and IFN-γ increased immunosuppressive protein such as HGF, TSG-6, PGE2 and TGF-β in EVs. Moreover, the anti-inflammatory effect of EVs was improved through pretreatment with inflammatory cytokines. Importantly, EVs obtained from primed stem cells effectively induced macrophage polarization toward an anti-inflammatory M2 phenotype and suppressed activated immunity by enhancing regulatory T cells in inflamed colon in mice. Our results provide a new and effective therapy for the EVs obtained from ASC stimulated with TNF-α and IFN-γ against not only IBD, but also immune-mediated disease. Nature Publishing Group UK 2020-02-07 /pmc/articles/PMC7005871/ /pubmed/32034203 http://dx.doi.org/10.1038/s41598-020-58909-4 Text en © The Author(s) 2020 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/.
spellingShingle Article
An, Ju-Hyun
Li, Qiang
Bhang, Dong-Ha
Song, Woo-Jin
Youn, Hwa-Young
TNF-α and INF-γ primed canine stem cell-derived extracellular vesicles alleviate experimental murine colitis
title TNF-α and INF-γ primed canine stem cell-derived extracellular vesicles alleviate experimental murine colitis
title_full TNF-α and INF-γ primed canine stem cell-derived extracellular vesicles alleviate experimental murine colitis
title_fullStr TNF-α and INF-γ primed canine stem cell-derived extracellular vesicles alleviate experimental murine colitis
title_full_unstemmed TNF-α and INF-γ primed canine stem cell-derived extracellular vesicles alleviate experimental murine colitis
title_short TNF-α and INF-γ primed canine stem cell-derived extracellular vesicles alleviate experimental murine colitis
title_sort tnf-α and inf-γ primed canine stem cell-derived extracellular vesicles alleviate experimental murine colitis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7005871/
https://www.ncbi.nlm.nih.gov/pubmed/32034203
http://dx.doi.org/10.1038/s41598-020-58909-4
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