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Boosting the Biogenesis and Secretion of Mesenchymal Stem Cell-Derived Exosomes

A limitation of using exosomes to their fullest potential is their limited secretion from cells, a major bottleneck to efficient exosome production and application. This is especially true for mesenchymal stem cells (MSCs), which can self-renew but have a limited expansion capacity, undergoing senes...

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Detalles Bibliográficos
Autores principales: Wang, Jinli, Bonacquisti, Emily E., Brown, Adam D., Nguyen, Juliane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7140620/
https://www.ncbi.nlm.nih.gov/pubmed/32182815
http://dx.doi.org/10.3390/cells9030660
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author Wang, Jinli
Bonacquisti, Emily E.
Brown, Adam D.
Nguyen, Juliane
author_facet Wang, Jinli
Bonacquisti, Emily E.
Brown, Adam D.
Nguyen, Juliane
author_sort Wang, Jinli
collection PubMed
description A limitation of using exosomes to their fullest potential is their limited secretion from cells, a major bottleneck to efficient exosome production and application. This is especially true for mesenchymal stem cells (MSCs), which can self-renew but have a limited expansion capacity, undergoing senescence after only a few passages, with exosomes derived from senescent stem cells showing impaired regenerative capacity compared to young cells. Here, we examined the effects of small molecule modulators capable of enhancing exosome secretion from MSCs. The treatment of MSCs with a combination of N-methyldopamine and norepinephrine robustly increased exosome production by three-fold without altering the ability of the MSC exosomes to induce angiogenesis, polarize macrophages to an anti-inflammatory phenotype, or downregulate collagen expression. These small molecule modulators provide a promising means to increase exosome production by MSCs.
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spelling pubmed-71406202020-04-13 Boosting the Biogenesis and Secretion of Mesenchymal Stem Cell-Derived Exosomes Wang, Jinli Bonacquisti, Emily E. Brown, Adam D. Nguyen, Juliane Cells Article A limitation of using exosomes to their fullest potential is their limited secretion from cells, a major bottleneck to efficient exosome production and application. This is especially true for mesenchymal stem cells (MSCs), which can self-renew but have a limited expansion capacity, undergoing senescence after only a few passages, with exosomes derived from senescent stem cells showing impaired regenerative capacity compared to young cells. Here, we examined the effects of small molecule modulators capable of enhancing exosome secretion from MSCs. The treatment of MSCs with a combination of N-methyldopamine and norepinephrine robustly increased exosome production by three-fold without altering the ability of the MSC exosomes to induce angiogenesis, polarize macrophages to an anti-inflammatory phenotype, or downregulate collagen expression. These small molecule modulators provide a promising means to increase exosome production by MSCs. MDPI 2020-03-09 /pmc/articles/PMC7140620/ /pubmed/32182815 http://dx.doi.org/10.3390/cells9030660 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Wang, Jinli
Bonacquisti, Emily E.
Brown, Adam D.
Nguyen, Juliane
Boosting the Biogenesis and Secretion of Mesenchymal Stem Cell-Derived Exosomes
title Boosting the Biogenesis and Secretion of Mesenchymal Stem Cell-Derived Exosomes
title_full Boosting the Biogenesis and Secretion of Mesenchymal Stem Cell-Derived Exosomes
title_fullStr Boosting the Biogenesis and Secretion of Mesenchymal Stem Cell-Derived Exosomes
title_full_unstemmed Boosting the Biogenesis and Secretion of Mesenchymal Stem Cell-Derived Exosomes
title_short Boosting the Biogenesis and Secretion of Mesenchymal Stem Cell-Derived Exosomes
title_sort boosting the biogenesis and secretion of mesenchymal stem cell-derived exosomes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7140620/
https://www.ncbi.nlm.nih.gov/pubmed/32182815
http://dx.doi.org/10.3390/cells9030660
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