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Alginate encapsulated multipotent adult progenitor cells promote corneal stromal cell activation via release of soluble factors
To reduce the increasing need for corneal transplantation, attempts are currently aiming to restore corneal clarity, one potent source of cells are multipotent adult progenitor cells (MAPC(®)). These cells release a powerful cocktail of paracrine factors that can guide wound healing and tissue regen...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6128465/ https://www.ncbi.nlm.nih.gov/pubmed/30192833 http://dx.doi.org/10.1371/journal.pone.0202118 |
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author | Al-Jaibaji, Olla Swioklo, Stephen Gijbels, Kristel Vaes, Bart Figueiredo, Francisco C. Connon, Che J. |
author_facet | Al-Jaibaji, Olla Swioklo, Stephen Gijbels, Kristel Vaes, Bart Figueiredo, Francisco C. Connon, Che J. |
author_sort | Al-Jaibaji, Olla |
collection | PubMed |
description | To reduce the increasing need for corneal transplantation, attempts are currently aiming to restore corneal clarity, one potent source of cells are multipotent adult progenitor cells (MAPC(®)). These cells release a powerful cocktail of paracrine factors that can guide wound healing and tissue regeneration. However, their role in corneal regeneration has been overlooked. Thus, we sought to explore the potential of combining the cytoprotective storage feature of alginate, with MAPC to generate a storable cell-laden gel for corneal wound healing. 72 hours following hypothermic storage, alginate encapsulation was shown to maintain MAPC viability at either 4 or 15°C. Encapsulated MAPC (2 x10(6) cells/mL) stored at 15°C presented the optimum temperature that allowed for cell recovery. These cells had the ability to reattach to tissue culture plastic whilst exhibiting normal phenotype and this was maintained in serum-free and xenobiotic-free medium. Furthermore, corneal stromal cells presented a significant decrease in scratch-wounds in the presence of alginate encapsulated MAPC compared to a no-cell control (p = 0.018). This study shows that immobilization of MAPC within an alginate hydrogel does not hinder their ability to affect a secondary cell population via soluble factors and that these effects are successfully retained following hypothermic storage. |
format | Online Article Text |
id | pubmed-6128465 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-61284652018-09-15 Alginate encapsulated multipotent adult progenitor cells promote corneal stromal cell activation via release of soluble factors Al-Jaibaji, Olla Swioklo, Stephen Gijbels, Kristel Vaes, Bart Figueiredo, Francisco C. Connon, Che J. PLoS One Research Article To reduce the increasing need for corneal transplantation, attempts are currently aiming to restore corneal clarity, one potent source of cells are multipotent adult progenitor cells (MAPC(®)). These cells release a powerful cocktail of paracrine factors that can guide wound healing and tissue regeneration. However, their role in corneal regeneration has been overlooked. Thus, we sought to explore the potential of combining the cytoprotective storage feature of alginate, with MAPC to generate a storable cell-laden gel for corneal wound healing. 72 hours following hypothermic storage, alginate encapsulation was shown to maintain MAPC viability at either 4 or 15°C. Encapsulated MAPC (2 x10(6) cells/mL) stored at 15°C presented the optimum temperature that allowed for cell recovery. These cells had the ability to reattach to tissue culture plastic whilst exhibiting normal phenotype and this was maintained in serum-free and xenobiotic-free medium. Furthermore, corneal stromal cells presented a significant decrease in scratch-wounds in the presence of alginate encapsulated MAPC compared to a no-cell control (p = 0.018). This study shows that immobilization of MAPC within an alginate hydrogel does not hinder their ability to affect a secondary cell population via soluble factors and that these effects are successfully retained following hypothermic storage. Public Library of Science 2018-09-07 /pmc/articles/PMC6128465/ /pubmed/30192833 http://dx.doi.org/10.1371/journal.pone.0202118 Text en © 2018 Al-Jaibaji et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Al-Jaibaji, Olla Swioklo, Stephen Gijbels, Kristel Vaes, Bart Figueiredo, Francisco C. Connon, Che J. Alginate encapsulated multipotent adult progenitor cells promote corneal stromal cell activation via release of soluble factors |
title | Alginate encapsulated multipotent adult progenitor cells promote corneal stromal cell activation via release of soluble factors |
title_full | Alginate encapsulated multipotent adult progenitor cells promote corneal stromal cell activation via release of soluble factors |
title_fullStr | Alginate encapsulated multipotent adult progenitor cells promote corneal stromal cell activation via release of soluble factors |
title_full_unstemmed | Alginate encapsulated multipotent adult progenitor cells promote corneal stromal cell activation via release of soluble factors |
title_short | Alginate encapsulated multipotent adult progenitor cells promote corneal stromal cell activation via release of soluble factors |
title_sort | alginate encapsulated multipotent adult progenitor cells promote corneal stromal cell activation via release of soluble factors |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6128465/ https://www.ncbi.nlm.nih.gov/pubmed/30192833 http://dx.doi.org/10.1371/journal.pone.0202118 |
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