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Immunological and Differentiation Properties of Amniotic Cells Are Retained After Immobilization in Pectin Gel

Mesenchymal stromal cells from the human amniotic membrane (i.e., human amniotic mesenchymal stromal cells [hAMSCs]) of term placenta are increasingly attracting attention for their applications in regenerative medicine. Osteochondral defects represent a major clinical problem with lifelong chronic...

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Autores principales: Silini, Antonietta R., Spoldi, Valentina, De Munari, Silvia, Vertua, Elsa, Munarin, Fabiola, Petrini, Paola, Farè, Silvia, Parolini, Ornella
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6434488/
https://www.ncbi.nlm.nih.gov/pubmed/29562782
http://dx.doi.org/10.1177/0963689717738786
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author Silini, Antonietta R.
Spoldi, Valentina
De Munari, Silvia
Vertua, Elsa
Munarin, Fabiola
Petrini, Paola
Farè, Silvia
Parolini, Ornella
author_facet Silini, Antonietta R.
Spoldi, Valentina
De Munari, Silvia
Vertua, Elsa
Munarin, Fabiola
Petrini, Paola
Farè, Silvia
Parolini, Ornella
author_sort Silini, Antonietta R.
collection PubMed
description Mesenchymal stromal cells from the human amniotic membrane (i.e., human amniotic mesenchymal stromal cells [hAMSCs]) of term placenta are increasingly attracting attention for their applications in regenerative medicine. Osteochondral defects represent a major clinical problem with lifelong chronic pain and compromised quality of life. Great promise for osteochondral regeneration is held in hydrogel-based constructs that have a flexible composition and mimic the physiological structure of cartilage. Cell loading within a hydrogel represents an advantage for regenerative purposes, but the encapsulation steps can modify cell properties. As pectin gels have also been explored as cell vehicles on 3D scaffolds, the aim of this study was to explore the possibility to include hAMSCs in pectin gel. Immobilization of hAMSCs into pectin gels could expand their application in cell-based bioengineering strategies. hAMSCs were analyzed for their viability and recovery from the pectin gel and for their ability to differentiate toward the osteogenic lineage and to maintain their immunological characteristics. When treated with a purposely designed pectin/hydroxyapatite gel biocomposite, hAMSCs retained their ability to differentiate toward the osteogenic lineage, did not induce an immune response, and retained their ability to reduce T cell proliferation. Taken together, these results suggest that hAMSCs could be used in combination to pectin gels for the study of novel osteochondral regeneration strategies.
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spelling pubmed-64344882019-04-01 Immunological and Differentiation Properties of Amniotic Cells Are Retained After Immobilization in Pectin Gel Silini, Antonietta R. Spoldi, Valentina De Munari, Silvia Vertua, Elsa Munarin, Fabiola Petrini, Paola Farè, Silvia Parolini, Ornella Cell Transplant Articles Mesenchymal stromal cells from the human amniotic membrane (i.e., human amniotic mesenchymal stromal cells [hAMSCs]) of term placenta are increasingly attracting attention for their applications in regenerative medicine. Osteochondral defects represent a major clinical problem with lifelong chronic pain and compromised quality of life. Great promise for osteochondral regeneration is held in hydrogel-based constructs that have a flexible composition and mimic the physiological structure of cartilage. Cell loading within a hydrogel represents an advantage for regenerative purposes, but the encapsulation steps can modify cell properties. As pectin gels have also been explored as cell vehicles on 3D scaffolds, the aim of this study was to explore the possibility to include hAMSCs in pectin gel. Immobilization of hAMSCs into pectin gels could expand their application in cell-based bioengineering strategies. hAMSCs were analyzed for their viability and recovery from the pectin gel and for their ability to differentiate toward the osteogenic lineage and to maintain their immunological characteristics. When treated with a purposely designed pectin/hydroxyapatite gel biocomposite, hAMSCs retained their ability to differentiate toward the osteogenic lineage, did not induce an immune response, and retained their ability to reduce T cell proliferation. Taken together, these results suggest that hAMSCs could be used in combination to pectin gels for the study of novel osteochondral regeneration strategies. SAGE Publications 2018-03-22 2018-01 /pmc/articles/PMC6434488/ /pubmed/29562782 http://dx.doi.org/10.1177/0963689717738786 Text en © The Author(s) 2018 http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Articles
Silini, Antonietta R.
Spoldi, Valentina
De Munari, Silvia
Vertua, Elsa
Munarin, Fabiola
Petrini, Paola
Farè, Silvia
Parolini, Ornella
Immunological and Differentiation Properties of Amniotic Cells Are Retained After Immobilization in Pectin Gel
title Immunological and Differentiation Properties of Amniotic Cells Are Retained After Immobilization in Pectin Gel
title_full Immunological and Differentiation Properties of Amniotic Cells Are Retained After Immobilization in Pectin Gel
title_fullStr Immunological and Differentiation Properties of Amniotic Cells Are Retained After Immobilization in Pectin Gel
title_full_unstemmed Immunological and Differentiation Properties of Amniotic Cells Are Retained After Immobilization in Pectin Gel
title_short Immunological and Differentiation Properties of Amniotic Cells Are Retained After Immobilization in Pectin Gel
title_sort immunological and differentiation properties of amniotic cells are retained after immobilization in pectin gel
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6434488/
https://www.ncbi.nlm.nih.gov/pubmed/29562782
http://dx.doi.org/10.1177/0963689717738786
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