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Priming of mesenchymal stem cells with a hydrosoluble form of curcumin allows keeping their mesenchymal properties for cell‐based therapy development
Mesenchymal stem cells are increasingly studied for their use as drug‐carrier in addition to their intrinsic potential for regenerative medicine. They could be used to transport molecules with a poor bioavailability such as curcumin in order to improve their clinical usage. This natural polyphenol,...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8107093/ https://www.ncbi.nlm.nih.gov/pubmed/33769687 http://dx.doi.org/10.1111/jcmm.16403 |
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author | Colin, Margaux Dechêne, Lola Ceusters, Justine Niesten, Ariane Demazy, Catherine Lagneaux, Laurence Zouaoui Boudjeltia, Karim Franck, Thierry Van Antwerpen, Pierre Renard, Patricia Mathieu, Véronique Serteyn, Didier |
author_facet | Colin, Margaux Dechêne, Lola Ceusters, Justine Niesten, Ariane Demazy, Catherine Lagneaux, Laurence Zouaoui Boudjeltia, Karim Franck, Thierry Van Antwerpen, Pierre Renard, Patricia Mathieu, Véronique Serteyn, Didier |
author_sort | Colin, Margaux |
collection | PubMed |
description | Mesenchymal stem cells are increasingly studied for their use as drug‐carrier in addition to their intrinsic potential for regenerative medicine. They could be used to transport molecules with a poor bioavailability such as curcumin in order to improve their clinical usage. This natural polyphenol, well‐known for its antioxidant and anti‐inflammatory properties, has a poor solubility that limits its clinical potential. For this purpose, the use of NDS27, a curcumin salt complexed with hydroxypropyl‐beta‐cyclodextrin (HPβCD), displaying an increased solubility in aqueous solution, is preferred. This study aims to evaluate the uptake of NDS27 into skeletal muscle‐derived mesenchymal stem cells (mdMSCs) and the effects of such uptake onto their mesenchymal properties. It appeared that the uptake of NDS27 into mdMSCs is concentration‐dependent and not time‐dependent. The use of a concentration of 7 µmol/L which does not affect the viability and proliferation also allows preservation of their adhesion, invasion and T cell immunomodulatory abilities. |
format | Online Article Text |
id | pubmed-8107093 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-81070932021-05-10 Priming of mesenchymal stem cells with a hydrosoluble form of curcumin allows keeping their mesenchymal properties for cell‐based therapy development Colin, Margaux Dechêne, Lola Ceusters, Justine Niesten, Ariane Demazy, Catherine Lagneaux, Laurence Zouaoui Boudjeltia, Karim Franck, Thierry Van Antwerpen, Pierre Renard, Patricia Mathieu, Véronique Serteyn, Didier J Cell Mol Med Short Communication Mesenchymal stem cells are increasingly studied for their use as drug‐carrier in addition to their intrinsic potential for regenerative medicine. They could be used to transport molecules with a poor bioavailability such as curcumin in order to improve their clinical usage. This natural polyphenol, well‐known for its antioxidant and anti‐inflammatory properties, has a poor solubility that limits its clinical potential. For this purpose, the use of NDS27, a curcumin salt complexed with hydroxypropyl‐beta‐cyclodextrin (HPβCD), displaying an increased solubility in aqueous solution, is preferred. This study aims to evaluate the uptake of NDS27 into skeletal muscle‐derived mesenchymal stem cells (mdMSCs) and the effects of such uptake onto their mesenchymal properties. It appeared that the uptake of NDS27 into mdMSCs is concentration‐dependent and not time‐dependent. The use of a concentration of 7 µmol/L which does not affect the viability and proliferation also allows preservation of their adhesion, invasion and T cell immunomodulatory abilities. John Wiley and Sons Inc. 2021-03-26 2021-05 /pmc/articles/PMC8107093/ /pubmed/33769687 http://dx.doi.org/10.1111/jcmm.16403 Text en © 2021 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Short Communication Colin, Margaux Dechêne, Lola Ceusters, Justine Niesten, Ariane Demazy, Catherine Lagneaux, Laurence Zouaoui Boudjeltia, Karim Franck, Thierry Van Antwerpen, Pierre Renard, Patricia Mathieu, Véronique Serteyn, Didier Priming of mesenchymal stem cells with a hydrosoluble form of curcumin allows keeping their mesenchymal properties for cell‐based therapy development |
title | Priming of mesenchymal stem cells with a hydrosoluble form of curcumin allows keeping their mesenchymal properties for cell‐based therapy development |
title_full | Priming of mesenchymal stem cells with a hydrosoluble form of curcumin allows keeping their mesenchymal properties for cell‐based therapy development |
title_fullStr | Priming of mesenchymal stem cells with a hydrosoluble form of curcumin allows keeping their mesenchymal properties for cell‐based therapy development |
title_full_unstemmed | Priming of mesenchymal stem cells with a hydrosoluble form of curcumin allows keeping their mesenchymal properties for cell‐based therapy development |
title_short | Priming of mesenchymal stem cells with a hydrosoluble form of curcumin allows keeping their mesenchymal properties for cell‐based therapy development |
title_sort | priming of mesenchymal stem cells with a hydrosoluble form of curcumin allows keeping their mesenchymal properties for cell‐based therapy development |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8107093/ https://www.ncbi.nlm.nih.gov/pubmed/33769687 http://dx.doi.org/10.1111/jcmm.16403 |
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