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Chitosan-based hydrogel to support the paracrine activity of mesenchymal stem cells in spinal cord injury treatment
Advanced therapies which combine cells with biomaterial-based carriers are recognized as an emerging and powerful method to treat challenging diseases, such as spinal cord injury (SCI). By enhancing transplanted cell survival and grafting, biomimetic hydrogels can be properly engineered to encapsula...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6483991/ https://www.ncbi.nlm.nih.gov/pubmed/31024032 http://dx.doi.org/10.1038/s41598-019-42848-w |
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author | Boido, M. Ghibaudi, M. Gentile, P. Favaro, E. Fusaro, R. Tonda-Turo, C. |
author_facet | Boido, M. Ghibaudi, M. Gentile, P. Favaro, E. Fusaro, R. Tonda-Turo, C. |
author_sort | Boido, M. |
collection | PubMed |
description | Advanced therapies which combine cells with biomaterial-based carriers are recognized as an emerging and powerful method to treat challenging diseases, such as spinal cord injury (SCI). By enhancing transplanted cell survival and grafting, biomimetic hydrogels can be properly engineered to encapsulate cells and locate them at the injured site in a minimally invasive way. In this work, chitosan (CS) based hydrogels were developed to host mesenchymal stem cells (MSCs), since their paracrine action can therapeutically enhance the SC regeneration, limiting the formation of a glial scar and reducing cell death at the injured site. An injectable and highly permeable CS-based hydrogel was fabricated having a rapid gelation upon temperature increase from 0 to 37 °C. CS was selected as former material both for its high biocompatibility that guarantees the proper environment for MSCs survival and for its ability to provide anti-inflammatory and anti-oxidant cues. MSCs were mixed with the hydrogel solution prior to gelation. MSC viability was not affected by the CS hydrogel and encapsulated MSCs were able to release MSC-vesicles as well as to maintain their anti-oxidant features. Finally, preliminary in vivo tests on SCI mice revealed good handling of the CS solution loading MSCs during implantation and high encapsulated MSCs survival after 7 days. |
format | Online Article Text |
id | pubmed-6483991 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64839912019-05-07 Chitosan-based hydrogel to support the paracrine activity of mesenchymal stem cells in spinal cord injury treatment Boido, M. Ghibaudi, M. Gentile, P. Favaro, E. Fusaro, R. Tonda-Turo, C. Sci Rep Article Advanced therapies which combine cells with biomaterial-based carriers are recognized as an emerging and powerful method to treat challenging diseases, such as spinal cord injury (SCI). By enhancing transplanted cell survival and grafting, biomimetic hydrogels can be properly engineered to encapsulate cells and locate them at the injured site in a minimally invasive way. In this work, chitosan (CS) based hydrogels were developed to host mesenchymal stem cells (MSCs), since their paracrine action can therapeutically enhance the SC regeneration, limiting the formation of a glial scar and reducing cell death at the injured site. An injectable and highly permeable CS-based hydrogel was fabricated having a rapid gelation upon temperature increase from 0 to 37 °C. CS was selected as former material both for its high biocompatibility that guarantees the proper environment for MSCs survival and for its ability to provide anti-inflammatory and anti-oxidant cues. MSCs were mixed with the hydrogel solution prior to gelation. MSC viability was not affected by the CS hydrogel and encapsulated MSCs were able to release MSC-vesicles as well as to maintain their anti-oxidant features. Finally, preliminary in vivo tests on SCI mice revealed good handling of the CS solution loading MSCs during implantation and high encapsulated MSCs survival after 7 days. Nature Publishing Group UK 2019-04-25 /pmc/articles/PMC6483991/ /pubmed/31024032 http://dx.doi.org/10.1038/s41598-019-42848-w Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Boido, M. Ghibaudi, M. Gentile, P. Favaro, E. Fusaro, R. Tonda-Turo, C. Chitosan-based hydrogel to support the paracrine activity of mesenchymal stem cells in spinal cord injury treatment |
title | Chitosan-based hydrogel to support the paracrine activity of mesenchymal stem cells in spinal cord injury treatment |
title_full | Chitosan-based hydrogel to support the paracrine activity of mesenchymal stem cells in spinal cord injury treatment |
title_fullStr | Chitosan-based hydrogel to support the paracrine activity of mesenchymal stem cells in spinal cord injury treatment |
title_full_unstemmed | Chitosan-based hydrogel to support the paracrine activity of mesenchymal stem cells in spinal cord injury treatment |
title_short | Chitosan-based hydrogel to support the paracrine activity of mesenchymal stem cells in spinal cord injury treatment |
title_sort | chitosan-based hydrogel to support the paracrine activity of mesenchymal stem cells in spinal cord injury treatment |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6483991/ https://www.ncbi.nlm.nih.gov/pubmed/31024032 http://dx.doi.org/10.1038/s41598-019-42848-w |
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