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Enhancement of therapeutic potential of mesenchymal stem cell-derived extracellular vesicles

After the initial investigations into applications of mesenchymal stem cells (MSCs) for cell therapy, there was increased interest in their secreted soluble factors. Following studies of MSCs and their secreted factors, extracellular vesicles (EVs) released from MSCs have emerged as a new mode of in...

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Autores principales: Park, Kyong-Su, Bandeira, Elga, Shelke, Ganesh V., Lässer, Cecilia, Lötvall, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6757418/
https://www.ncbi.nlm.nih.gov/pubmed/31547882
http://dx.doi.org/10.1186/s13287-019-1398-3
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author Park, Kyong-Su
Bandeira, Elga
Shelke, Ganesh V.
Lässer, Cecilia
Lötvall, Jan
author_facet Park, Kyong-Su
Bandeira, Elga
Shelke, Ganesh V.
Lässer, Cecilia
Lötvall, Jan
author_sort Park, Kyong-Su
collection PubMed
description After the initial investigations into applications of mesenchymal stem cells (MSCs) for cell therapy, there was increased interest in their secreted soluble factors. Following studies of MSCs and their secreted factors, extracellular vesicles (EVs) released from MSCs have emerged as a new mode of intercellular crosstalk. MSC-derived EVs have been identified as essential signaling mediators under both physiological and pathological conditions, and they appear to be responsible for many of the therapeutic effects of MSCs. In several in vitro and in vivo models, EVs have been observed to have supportive functions in modulating the immune system, mainly mediated by EV-associated proteins and nucleic acids. Moreover, stimulation of MSCs with biophysical or biochemical cues, including EVs from other cells, has been shown to influence the contents and biological activities of subsequent MSC-derived EVs. This review provides on overview of the contents of MSC-derived EVs in terms of their supportive effects, and it provides different perspectives on the manipulation of MSCs to improve the secretion of EVs and subsequent EV-mediated activities. In this review, we discuss the possibilities for manipulating MSCs for EV-based cell therapy and for using EVs to affect the expression of elements of interest in MSCs. In this way, we provide a clear perspective on the state of the art of EVs in cell therapy focusing on MSCs, and we raise pertinent questions and suggestions for knowledge gaps to be filled. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13287-019-1398-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-67574182019-09-30 Enhancement of therapeutic potential of mesenchymal stem cell-derived extracellular vesicles Park, Kyong-Su Bandeira, Elga Shelke, Ganesh V. Lässer, Cecilia Lötvall, Jan Stem Cell Res Ther Review After the initial investigations into applications of mesenchymal stem cells (MSCs) for cell therapy, there was increased interest in their secreted soluble factors. Following studies of MSCs and their secreted factors, extracellular vesicles (EVs) released from MSCs have emerged as a new mode of intercellular crosstalk. MSC-derived EVs have been identified as essential signaling mediators under both physiological and pathological conditions, and they appear to be responsible for many of the therapeutic effects of MSCs. In several in vitro and in vivo models, EVs have been observed to have supportive functions in modulating the immune system, mainly mediated by EV-associated proteins and nucleic acids. Moreover, stimulation of MSCs with biophysical or biochemical cues, including EVs from other cells, has been shown to influence the contents and biological activities of subsequent MSC-derived EVs. This review provides on overview of the contents of MSC-derived EVs in terms of their supportive effects, and it provides different perspectives on the manipulation of MSCs to improve the secretion of EVs and subsequent EV-mediated activities. In this review, we discuss the possibilities for manipulating MSCs for EV-based cell therapy and for using EVs to affect the expression of elements of interest in MSCs. In this way, we provide a clear perspective on the state of the art of EVs in cell therapy focusing on MSCs, and we raise pertinent questions and suggestions for knowledge gaps to be filled. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13287-019-1398-3) contains supplementary material, which is available to authorized users. BioMed Central 2019-09-23 /pmc/articles/PMC6757418/ /pubmed/31547882 http://dx.doi.org/10.1186/s13287-019-1398-3 Text en © The Author(s). 2019 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
Park, Kyong-Su
Bandeira, Elga
Shelke, Ganesh V.
Lässer, Cecilia
Lötvall, Jan
Enhancement of therapeutic potential of mesenchymal stem cell-derived extracellular vesicles
title Enhancement of therapeutic potential of mesenchymal stem cell-derived extracellular vesicles
title_full Enhancement of therapeutic potential of mesenchymal stem cell-derived extracellular vesicles
title_fullStr Enhancement of therapeutic potential of mesenchymal stem cell-derived extracellular vesicles
title_full_unstemmed Enhancement of therapeutic potential of mesenchymal stem cell-derived extracellular vesicles
title_short Enhancement of therapeutic potential of mesenchymal stem cell-derived extracellular vesicles
title_sort enhancement of therapeutic potential of mesenchymal stem cell-derived extracellular vesicles
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6757418/
https://www.ncbi.nlm.nih.gov/pubmed/31547882
http://dx.doi.org/10.1186/s13287-019-1398-3
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