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Recellularization of Decellularized Lung Scaffolds Is Enhanced by Dynamic Suspension Culture
Strategies are needed to improve repopulation of decellularized lung scaffolds with stromal and functional epithelial cells. We demonstrate that decellularized mouse lungs recellularized in a dynamic low fluid shear suspension bioreactor, termed the rotating wall vessel (RWV), contained more cells w...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4427280/ https://www.ncbi.nlm.nih.gov/pubmed/25962111 http://dx.doi.org/10.1371/journal.pone.0126846 |
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author | Crabbé, Aurélie Liu, Yulong Sarker, Shameema F. Bonenfant, Nicholas R. Barrila, Jennifer Borg, Zachary D. Lee, James J. Weiss, Daniel J. Nickerson, Cheryl A. |
author_facet | Crabbé, Aurélie Liu, Yulong Sarker, Shameema F. Bonenfant, Nicholas R. Barrila, Jennifer Borg, Zachary D. Lee, James J. Weiss, Daniel J. Nickerson, Cheryl A. |
author_sort | Crabbé, Aurélie |
collection | PubMed |
description | Strategies are needed to improve repopulation of decellularized lung scaffolds with stromal and functional epithelial cells. We demonstrate that decellularized mouse lungs recellularized in a dynamic low fluid shear suspension bioreactor, termed the rotating wall vessel (RWV), contained more cells with decreased apoptosis, increased proliferation and enhanced levels of total RNA compared to static recellularization conditions. These results were observed with two relevant mouse cell types: bone marrow-derived mesenchymal stromal (stem) cells (MSCs) and alveolar type II cells (C10). In addition, MSCs cultured in decellularized lungs under static but not bioreactor conditions formed multilayered aggregates. Gene expression and immunohistochemical analyses suggested differentiation of MSCs into collagen I-producing fibroblast-like cells in the bioreactor, indicating enhanced potential for remodeling of the decellularized scaffold matrix. In conclusion, dynamic suspension culture is promising for enhancing repopulation of decellularized lungs, and could contribute to remodeling the extracellular matrix of the scaffolds with subsequent effects on differentiation and functionality of inoculated cells. |
format | Online Article Text |
id | pubmed-4427280 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-44272802015-05-21 Recellularization of Decellularized Lung Scaffolds Is Enhanced by Dynamic Suspension Culture Crabbé, Aurélie Liu, Yulong Sarker, Shameema F. Bonenfant, Nicholas R. Barrila, Jennifer Borg, Zachary D. Lee, James J. Weiss, Daniel J. Nickerson, Cheryl A. PLoS One Research Article Strategies are needed to improve repopulation of decellularized lung scaffolds with stromal and functional epithelial cells. We demonstrate that decellularized mouse lungs recellularized in a dynamic low fluid shear suspension bioreactor, termed the rotating wall vessel (RWV), contained more cells with decreased apoptosis, increased proliferation and enhanced levels of total RNA compared to static recellularization conditions. These results were observed with two relevant mouse cell types: bone marrow-derived mesenchymal stromal (stem) cells (MSCs) and alveolar type II cells (C10). In addition, MSCs cultured in decellularized lungs under static but not bioreactor conditions formed multilayered aggregates. Gene expression and immunohistochemical analyses suggested differentiation of MSCs into collagen I-producing fibroblast-like cells in the bioreactor, indicating enhanced potential for remodeling of the decellularized scaffold matrix. In conclusion, dynamic suspension culture is promising for enhancing repopulation of decellularized lungs, and could contribute to remodeling the extracellular matrix of the scaffolds with subsequent effects on differentiation and functionality of inoculated cells. Public Library of Science 2015-05-11 /pmc/articles/PMC4427280/ /pubmed/25962111 http://dx.doi.org/10.1371/journal.pone.0126846 Text en © 2015 Crabbé 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Crabbé, Aurélie Liu, Yulong Sarker, Shameema F. Bonenfant, Nicholas R. Barrila, Jennifer Borg, Zachary D. Lee, James J. Weiss, Daniel J. Nickerson, Cheryl A. Recellularization of Decellularized Lung Scaffolds Is Enhanced by Dynamic Suspension Culture |
title | Recellularization of Decellularized Lung Scaffolds Is Enhanced by Dynamic Suspension Culture |
title_full | Recellularization of Decellularized Lung Scaffolds Is Enhanced by Dynamic Suspension Culture |
title_fullStr | Recellularization of Decellularized Lung Scaffolds Is Enhanced by Dynamic Suspension Culture |
title_full_unstemmed | Recellularization of Decellularized Lung Scaffolds Is Enhanced by Dynamic Suspension Culture |
title_short | Recellularization of Decellularized Lung Scaffolds Is Enhanced by Dynamic Suspension Culture |
title_sort | recellularization of decellularized lung scaffolds is enhanced by dynamic suspension culture |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4427280/ https://www.ncbi.nlm.nih.gov/pubmed/25962111 http://dx.doi.org/10.1371/journal.pone.0126846 |
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