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Mouse placental scaffolds: a three-dimensional environment model for recellularization
The rich extracellular matrix (ECM) and availability make placenta eligible as alternative biomaterial source. Herein we produced placental mouse scaffolds by decellularization, and structure, composition, and cytocompatibility were evaluated to be considered as a biomaterial. We obtained a cell-fre...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6689918/ https://www.ncbi.nlm.nih.gov/pubmed/31448074 http://dx.doi.org/10.1177/2041731419867962 |
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author | Barreto, Rodrigo SN Romagnolli, Patricia Fratini, Paula Mess, Andrea Maria Miglino, Maria Angelica |
author_facet | Barreto, Rodrigo SN Romagnolli, Patricia Fratini, Paula Mess, Andrea Maria Miglino, Maria Angelica |
author_sort | Barreto, Rodrigo SN |
collection | PubMed |
description | The rich extracellular matrix (ECM) and availability make placenta eligible as alternative biomaterial source. Herein we produced placental mouse scaffolds by decellularization, and structure, composition, and cytocompatibility were evaluated to be considered as a biomaterial. We obtained a cell-free scaffold containing 9.42 ± 5.2 ng dsDNA per mg of ECM, presenting well-preserved structure and composition. Proteoglycans were widespread throughout ECM without cell nuclei and cell remnants. Collagen I, weak in native placenta, clearly appears in the scaffold after recellularization, opposite distribution was observed for collagen III. Fibronectin was well-observed in placental scaffolds whereas laminin and collagen IV were strong expressed. Placental scaffolds recellularization potential was confirmed after mouse embryonic fibroblasts 3D dynamic culture, resulting in massive scaffold repopulation with cell–cell interactions, cell-matrix adhesion, and maintenance of natural morphology. Our small size scaffolds provide a useful tool for tissue engineering to produce grafts and organ fragments, as well as for cellular biology purposes for tridimensional culture substrate. |
format | Online Article Text |
id | pubmed-6689918 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-66899182019-08-23 Mouse placental scaffolds: a three-dimensional environment model for recellularization Barreto, Rodrigo SN Romagnolli, Patricia Fratini, Paula Mess, Andrea Maria Miglino, Maria Angelica J Tissue Eng Original Article The rich extracellular matrix (ECM) and availability make placenta eligible as alternative biomaterial source. Herein we produced placental mouse scaffolds by decellularization, and structure, composition, and cytocompatibility were evaluated to be considered as a biomaterial. We obtained a cell-free scaffold containing 9.42 ± 5.2 ng dsDNA per mg of ECM, presenting well-preserved structure and composition. Proteoglycans were widespread throughout ECM without cell nuclei and cell remnants. Collagen I, weak in native placenta, clearly appears in the scaffold after recellularization, opposite distribution was observed for collagen III. Fibronectin was well-observed in placental scaffolds whereas laminin and collagen IV were strong expressed. Placental scaffolds recellularization potential was confirmed after mouse embryonic fibroblasts 3D dynamic culture, resulting in massive scaffold repopulation with cell–cell interactions, cell-matrix adhesion, and maintenance of natural morphology. Our small size scaffolds provide a useful tool for tissue engineering to produce grafts and organ fragments, as well as for cellular biology purposes for tridimensional culture substrate. SAGE Publications 2019-08-08 /pmc/articles/PMC6689918/ /pubmed/31448074 http://dx.doi.org/10.1177/2041731419867962 Text en © The Author(s) 2019 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 | Original Article Barreto, Rodrigo SN Romagnolli, Patricia Fratini, Paula Mess, Andrea Maria Miglino, Maria Angelica Mouse placental scaffolds: a three-dimensional environment model for recellularization |
title | Mouse placental scaffolds: a three-dimensional environment model for recellularization |
title_full | Mouse placental scaffolds: a three-dimensional environment model for recellularization |
title_fullStr | Mouse placental scaffolds: a three-dimensional environment model for recellularization |
title_full_unstemmed | Mouse placental scaffolds: a three-dimensional environment model for recellularization |
title_short | Mouse placental scaffolds: a three-dimensional environment model for recellularization |
title_sort | mouse placental scaffolds: a three-dimensional environment model for recellularization |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6689918/ https://www.ncbi.nlm.nih.gov/pubmed/31448074 http://dx.doi.org/10.1177/2041731419867962 |
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