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Therapeutic potential of products derived from mesenchymal stem/stromal cells in pulmonary disease
Multipotent mesenchymal stem/stromal cells (MSCs) possess robust self-renewal characteristics and the ability to differentiate into tissue-specific cells. Their therapeutic potential appears promising as evident from their efficacy in several animal models of pulmonary disorders as well as early-pha...
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/PMC6234778/ https://www.ncbi.nlm.nih.gov/pubmed/30413158 http://dx.doi.org/10.1186/s12931-018-0921-x |
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author | Mohammadipoor, Arezoo Antebi, Ben Batchinsky, Andriy I. Cancio, Leopoldo C. |
author_facet | Mohammadipoor, Arezoo Antebi, Ben Batchinsky, Andriy I. Cancio, Leopoldo C. |
author_sort | Mohammadipoor, Arezoo |
collection | PubMed |
description | Multipotent mesenchymal stem/stromal cells (MSCs) possess robust self-renewal characteristics and the ability to differentiate into tissue-specific cells. Their therapeutic potential appears promising as evident from their efficacy in several animal models of pulmonary disorders as well as early-phase clinical trials of acute respiratory distress syndrome (ARDS) and chronic obstructive pulmonary disease (COPD). Such therapeutic efficacy might be attributed to MSC-derived products (the “secretome”), namely conditioned media (CM) and extracellular vesicles (EVs), which have been shown to play pivotal roles in the regenerative function of MSCs. Importantly, the EVs secreted by MSCs can transfer a variety of bioactive factors to modulate the function of recipient cells via various mechanisms, including ligand-receptor interactions, direct membrane fusion, endocytosis, or phagocytosis. Herein, we review the current state-of-the-science of MSC-derived CM and EVs as potential therapeutic agents in lung diseases. We suggest that the MSC-derived secretome might be an appropriate therapeutic agent for treating aggressive pulmonary disorders because of biological and logistical advantages over live cell therapy. Nonetheless, further studies are warranted to elucidate the safety and efficacy of these components in combating pulmonary diseases. |
format | Online Article Text |
id | pubmed-6234778 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-62347782018-11-20 Therapeutic potential of products derived from mesenchymal stem/stromal cells in pulmonary disease Mohammadipoor, Arezoo Antebi, Ben Batchinsky, Andriy I. Cancio, Leopoldo C. Respir Res Review Multipotent mesenchymal stem/stromal cells (MSCs) possess robust self-renewal characteristics and the ability to differentiate into tissue-specific cells. Their therapeutic potential appears promising as evident from their efficacy in several animal models of pulmonary disorders as well as early-phase clinical trials of acute respiratory distress syndrome (ARDS) and chronic obstructive pulmonary disease (COPD). Such therapeutic efficacy might be attributed to MSC-derived products (the “secretome”), namely conditioned media (CM) and extracellular vesicles (EVs), which have been shown to play pivotal roles in the regenerative function of MSCs. Importantly, the EVs secreted by MSCs can transfer a variety of bioactive factors to modulate the function of recipient cells via various mechanisms, including ligand-receptor interactions, direct membrane fusion, endocytosis, or phagocytosis. Herein, we review the current state-of-the-science of MSC-derived CM and EVs as potential therapeutic agents in lung diseases. We suggest that the MSC-derived secretome might be an appropriate therapeutic agent for treating aggressive pulmonary disorders because of biological and logistical advantages over live cell therapy. Nonetheless, further studies are warranted to elucidate the safety and efficacy of these components in combating pulmonary diseases. BioMed Central 2018-11-09 2018 /pmc/articles/PMC6234778/ /pubmed/30413158 http://dx.doi.org/10.1186/s12931-018-0921-x 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 | Review Mohammadipoor, Arezoo Antebi, Ben Batchinsky, Andriy I. Cancio, Leopoldo C. Therapeutic potential of products derived from mesenchymal stem/stromal cells in pulmonary disease |
title | Therapeutic potential of products derived from mesenchymal stem/stromal cells in pulmonary disease |
title_full | Therapeutic potential of products derived from mesenchymal stem/stromal cells in pulmonary disease |
title_fullStr | Therapeutic potential of products derived from mesenchymal stem/stromal cells in pulmonary disease |
title_full_unstemmed | Therapeutic potential of products derived from mesenchymal stem/stromal cells in pulmonary disease |
title_short | Therapeutic potential of products derived from mesenchymal stem/stromal cells in pulmonary disease |
title_sort | therapeutic potential of products derived from mesenchymal stem/stromal cells in pulmonary disease |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6234778/ https://www.ncbi.nlm.nih.gov/pubmed/30413158 http://dx.doi.org/10.1186/s12931-018-0921-x |
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