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Exosomes derived from human adipose tissue-derived mesenchymal stem cells alleviate atopic dermatitis
Exosomes are nano-sized vesicles (30–200 nm) constantly released by almost all cells. The ability of exosomes to travel between cells and deliver their cargo, which includes lipids, proteins, and nucleic acids, makes them an appealing cell-free therapy option to treat multiple diseases. Here, we inv...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6042362/ https://www.ncbi.nlm.nih.gov/pubmed/29996938 http://dx.doi.org/10.1186/s13287-018-0939-5 |
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author | Cho, Byong Seung Kim, Jin Ock Ha, Dae Hyun Yi, Yong Weon |
author_facet | Cho, Byong Seung Kim, Jin Ock Ha, Dae Hyun Yi, Yong Weon |
author_sort | Cho, Byong Seung |
collection | PubMed |
description | Exosomes are nano-sized vesicles (30–200 nm) constantly released by almost all cells. The ability of exosomes to travel between cells and deliver their cargo, which includes lipids, proteins, and nucleic acids, makes them an appealing cell-free therapy option to treat multiple diseases. Here, we investigated for the first time whether human adipose tissue-derived mesenchymal stem cell-derived exosomes (ASC-exosomes) can ameliorate atopic dermatitis (AD) in an in vivo mouse model. When injected either intravenously (IV) or subcutaneously (SC) into NC/Nga mice treated with house dust mite antigens, ASC-exosomes were found to reduce pathological symptoms such as clinical score, the levels of serum IgE, the number of eosinophils in blood, and the infiltration of mast cells, CD86+, and CD206+ cells in skin lesions. ASC-exosomes also significantly reduced mRNA expression of various inflammatory cytokines such as interleukin (IL)-4, IL-23, IL-31, and tumor necrosis factor-α (TNF-α) in AD skin lesions of Nc/Nga mice. Taken together, these results suggest that ASC-exosomes can be a novel promising cell-free therapeutic modality for AD treatment. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13287-018-0939-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6042362 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-60423622018-07-13 Exosomes derived from human adipose tissue-derived mesenchymal stem cells alleviate atopic dermatitis Cho, Byong Seung Kim, Jin Ock Ha, Dae Hyun Yi, Yong Weon Stem Cell Res Ther Letter Exosomes are nano-sized vesicles (30–200 nm) constantly released by almost all cells. The ability of exosomes to travel between cells and deliver their cargo, which includes lipids, proteins, and nucleic acids, makes them an appealing cell-free therapy option to treat multiple diseases. Here, we investigated for the first time whether human adipose tissue-derived mesenchymal stem cell-derived exosomes (ASC-exosomes) can ameliorate atopic dermatitis (AD) in an in vivo mouse model. When injected either intravenously (IV) or subcutaneously (SC) into NC/Nga mice treated with house dust mite antigens, ASC-exosomes were found to reduce pathological symptoms such as clinical score, the levels of serum IgE, the number of eosinophils in blood, and the infiltration of mast cells, CD86+, and CD206+ cells in skin lesions. ASC-exosomes also significantly reduced mRNA expression of various inflammatory cytokines such as interleukin (IL)-4, IL-23, IL-31, and tumor necrosis factor-α (TNF-α) in AD skin lesions of Nc/Nga mice. Taken together, these results suggest that ASC-exosomes can be a novel promising cell-free therapeutic modality for AD treatment. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13287-018-0939-5) contains supplementary material, which is available to authorized users. BioMed Central 2018-07-11 /pmc/articles/PMC6042362/ /pubmed/29996938 http://dx.doi.org/10.1186/s13287-018-0939-5 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Letter Cho, Byong Seung Kim, Jin Ock Ha, Dae Hyun Yi, Yong Weon Exosomes derived from human adipose tissue-derived mesenchymal stem cells alleviate atopic dermatitis |
title | Exosomes derived from human adipose tissue-derived mesenchymal stem cells alleviate atopic dermatitis |
title_full | Exosomes derived from human adipose tissue-derived mesenchymal stem cells alleviate atopic dermatitis |
title_fullStr | Exosomes derived from human adipose tissue-derived mesenchymal stem cells alleviate atopic dermatitis |
title_full_unstemmed | Exosomes derived from human adipose tissue-derived mesenchymal stem cells alleviate atopic dermatitis |
title_short | Exosomes derived from human adipose tissue-derived mesenchymal stem cells alleviate atopic dermatitis |
title_sort | exosomes derived from human adipose tissue-derived mesenchymal stem cells alleviate atopic dermatitis |
topic | Letter |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6042362/ https://www.ncbi.nlm.nih.gov/pubmed/29996938 http://dx.doi.org/10.1186/s13287-018-0939-5 |
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