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Gadolinium-Labelled Cell Scaffolds to Follow-up Cell Transplantation by Magnetic Resonance Imaging
Cell scaffolds are often used in cell transplantation as they provide a solid structural support to implanted cells and can be bioengineered to mimic the native extracellular matrix. Gadolinium fluoride nanoparticles (Gd-NPs) as a contrast agent for Magnetic Resonance Imaging (MRI) were incorporated...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6787680/ https://www.ncbi.nlm.nih.gov/pubmed/31269673 http://dx.doi.org/10.3390/jfb10030028 |
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author | Catanzaro, Valeria Digilio, Giuseppe Capuana, Federico Padovan, Sergio Cutrin, Juan C. Carniato, Fabio Porta, Stefano Grange, Cristina Filipović, Nenad Stevanović, Magdalena |
author_facet | Catanzaro, Valeria Digilio, Giuseppe Capuana, Federico Padovan, Sergio Cutrin, Juan C. Carniato, Fabio Porta, Stefano Grange, Cristina Filipović, Nenad Stevanović, Magdalena |
author_sort | Catanzaro, Valeria |
collection | PubMed |
description | Cell scaffolds are often used in cell transplantation as they provide a solid structural support to implanted cells and can be bioengineered to mimic the native extracellular matrix. Gadolinium fluoride nanoparticles (Gd-NPs) as a contrast agent for Magnetic Resonance Imaging (MRI) were incorporated into poly(lactide-co-glycolide)/chitosan scaffolds to obtain Imaging Labelled Cell Scaffolds (ILCSs), having the shape of hollow spherical/ellipsoidal particles (200–600 μm diameter and 50–80 μm shell thickness). While Gd-NPs incorporated into microparticles do not provide any contrast enhancement in T(1)-weighted (T(1)w) MR images, ILCSs can release Gd-NPs in a controlled manner, thus activating MRI contrast. ILCSs seeded with human mesenchymal stromal cells (hMSCs) were xenografted subcutaneously into either immunocompromised and immunocompetent mice without any immunosuppressant treatments, and the transplants were followed-up in vivo by MRI for 18 days. Immunocompromised mice showed a progressive activation of MRI contrast within the implants due to the release of Gd-NPs in the extracellular matrix. Instead, immunocompetent mice showed poor activation of MRI contrast due to the encapsulation of ILCSs within fibrotic capsules and to the scavenging of released Gd-NPs by phagocytic cells. In conclusion, the MRI follow-up of cell xenografts can report the host cell response to the xenograft. However, it does not strictly report on the viability of transplanted hMSCs. |
format | Online Article Text |
id | pubmed-6787680 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-67876802019-10-16 Gadolinium-Labelled Cell Scaffolds to Follow-up Cell Transplantation by Magnetic Resonance Imaging Catanzaro, Valeria Digilio, Giuseppe Capuana, Federico Padovan, Sergio Cutrin, Juan C. Carniato, Fabio Porta, Stefano Grange, Cristina Filipović, Nenad Stevanović, Magdalena J Funct Biomater Article Cell scaffolds are often used in cell transplantation as they provide a solid structural support to implanted cells and can be bioengineered to mimic the native extracellular matrix. Gadolinium fluoride nanoparticles (Gd-NPs) as a contrast agent for Magnetic Resonance Imaging (MRI) were incorporated into poly(lactide-co-glycolide)/chitosan scaffolds to obtain Imaging Labelled Cell Scaffolds (ILCSs), having the shape of hollow spherical/ellipsoidal particles (200–600 μm diameter and 50–80 μm shell thickness). While Gd-NPs incorporated into microparticles do not provide any contrast enhancement in T(1)-weighted (T(1)w) MR images, ILCSs can release Gd-NPs in a controlled manner, thus activating MRI contrast. ILCSs seeded with human mesenchymal stromal cells (hMSCs) were xenografted subcutaneously into either immunocompromised and immunocompetent mice without any immunosuppressant treatments, and the transplants were followed-up in vivo by MRI for 18 days. Immunocompromised mice showed a progressive activation of MRI contrast within the implants due to the release of Gd-NPs in the extracellular matrix. Instead, immunocompetent mice showed poor activation of MRI contrast due to the encapsulation of ILCSs within fibrotic capsules and to the scavenging of released Gd-NPs by phagocytic cells. In conclusion, the MRI follow-up of cell xenografts can report the host cell response to the xenograft. However, it does not strictly report on the viability of transplanted hMSCs. MDPI 2019-07-02 /pmc/articles/PMC6787680/ /pubmed/31269673 http://dx.doi.org/10.3390/jfb10030028 Text en © 2019 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 Catanzaro, Valeria Digilio, Giuseppe Capuana, Federico Padovan, Sergio Cutrin, Juan C. Carniato, Fabio Porta, Stefano Grange, Cristina Filipović, Nenad Stevanović, Magdalena Gadolinium-Labelled Cell Scaffolds to Follow-up Cell Transplantation by Magnetic Resonance Imaging |
title | Gadolinium-Labelled Cell Scaffolds to Follow-up Cell Transplantation by Magnetic Resonance Imaging |
title_full | Gadolinium-Labelled Cell Scaffolds to Follow-up Cell Transplantation by Magnetic Resonance Imaging |
title_fullStr | Gadolinium-Labelled Cell Scaffolds to Follow-up Cell Transplantation by Magnetic Resonance Imaging |
title_full_unstemmed | Gadolinium-Labelled Cell Scaffolds to Follow-up Cell Transplantation by Magnetic Resonance Imaging |
title_short | Gadolinium-Labelled Cell Scaffolds to Follow-up Cell Transplantation by Magnetic Resonance Imaging |
title_sort | gadolinium-labelled cell scaffolds to follow-up cell transplantation by magnetic resonance imaging |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6787680/ https://www.ncbi.nlm.nih.gov/pubmed/31269673 http://dx.doi.org/10.3390/jfb10030028 |
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