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Pushing the Envelope in Tissue Engineering: Ex Vivo Production of Thick Vascularized Cardiac Extracellular Matrix Constructs
Functional vascularization is a prerequisite for cardiac tissue engineering of constructs with physiological thicknesses. We previously reported the successful preservation of main vascular conduits in isolated thick acellular porcine cardiac ventricular ECM (pcECM). We now unveil this scaffold'...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mary Ann Liebert, Inc.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4426298/ https://www.ncbi.nlm.nih.gov/pubmed/25602926 http://dx.doi.org/10.1089/ten.tea.2014.0477 |
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author | Sarig, Udi Nguyen, Evelyne Bao-Vi Wang, Yao Ting, Sherwin Bronshtein, Tomer Sarig, Hadar Dahan, Nitsan Gvirtz, Maskit Reuveny, Shaul Oh, Steve K.W. Scheper, Thomas Boey, Yin Chiang Freddy Venkatraman, Subbu S. Machluf, Marcelle |
author_facet | Sarig, Udi Nguyen, Evelyne Bao-Vi Wang, Yao Ting, Sherwin Bronshtein, Tomer Sarig, Hadar Dahan, Nitsan Gvirtz, Maskit Reuveny, Shaul Oh, Steve K.W. Scheper, Thomas Boey, Yin Chiang Freddy Venkatraman, Subbu S. Machluf, Marcelle |
author_sort | Sarig, Udi |
collection | PubMed |
description | Functional vascularization is a prerequisite for cardiac tissue engineering of constructs with physiological thicknesses. We previously reported the successful preservation of main vascular conduits in isolated thick acellular porcine cardiac ventricular ECM (pcECM). We now unveil this scaffold's potential in supporting human cardiomyocytes and promoting new blood vessel development ex vivo, providing long-term cell support in the construct bulk. A custom-designed perfusion bioreactor was developed to remodel such vascularization ex vivo, demonstrating, for the first time, functional angiogenesis in vitro with various stages of vessel maturation supporting up to 1.7 mm thick constructs. A robust methodology was developed to assess the pcECM maximal cell capacity, which resembled the human heart cell density. Taken together these results demonstrate feasibility of producing physiological-like constructs such as the thick pcECM suggested here as a prospective treatment for end-stage heart failure. Methodologies reported herein may also benefit other tissues, offering a valuable in vitro setting for “thick-tissue” engineering strategies toward large animal in vivo studies. |
format | Online Article Text |
id | pubmed-4426298 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Mary Ann Liebert, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-44262982015-05-27 Pushing the Envelope in Tissue Engineering: Ex Vivo Production of Thick Vascularized Cardiac Extracellular Matrix Constructs Sarig, Udi Nguyen, Evelyne Bao-Vi Wang, Yao Ting, Sherwin Bronshtein, Tomer Sarig, Hadar Dahan, Nitsan Gvirtz, Maskit Reuveny, Shaul Oh, Steve K.W. Scheper, Thomas Boey, Yin Chiang Freddy Venkatraman, Subbu S. Machluf, Marcelle Tissue Eng Part A Original Articles Functional vascularization is a prerequisite for cardiac tissue engineering of constructs with physiological thicknesses. We previously reported the successful preservation of main vascular conduits in isolated thick acellular porcine cardiac ventricular ECM (pcECM). We now unveil this scaffold's potential in supporting human cardiomyocytes and promoting new blood vessel development ex vivo, providing long-term cell support in the construct bulk. A custom-designed perfusion bioreactor was developed to remodel such vascularization ex vivo, demonstrating, for the first time, functional angiogenesis in vitro with various stages of vessel maturation supporting up to 1.7 mm thick constructs. A robust methodology was developed to assess the pcECM maximal cell capacity, which resembled the human heart cell density. Taken together these results demonstrate feasibility of producing physiological-like constructs such as the thick pcECM suggested here as a prospective treatment for end-stage heart failure. Methodologies reported herein may also benefit other tissues, offering a valuable in vitro setting for “thick-tissue” engineering strategies toward large animal in vivo studies. Mary Ann Liebert, Inc. 2015-05-01 2015-03-17 /pmc/articles/PMC4426298/ /pubmed/25602926 http://dx.doi.org/10.1089/ten.tea.2014.0477 Text en © Udi Sarig et al. 2015; Published by Mary Ann Liebert, Inc. This Open Access article is distributed under the terms of the Creative Commons Attribution Noncommercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Original Articles Sarig, Udi Nguyen, Evelyne Bao-Vi Wang, Yao Ting, Sherwin Bronshtein, Tomer Sarig, Hadar Dahan, Nitsan Gvirtz, Maskit Reuveny, Shaul Oh, Steve K.W. Scheper, Thomas Boey, Yin Chiang Freddy Venkatraman, Subbu S. Machluf, Marcelle Pushing the Envelope in Tissue Engineering: Ex Vivo Production of Thick Vascularized Cardiac Extracellular Matrix Constructs |
title | Pushing the Envelope in Tissue Engineering: Ex Vivo Production of Thick Vascularized Cardiac Extracellular Matrix Constructs |
title_full | Pushing the Envelope in Tissue Engineering: Ex Vivo Production of Thick Vascularized Cardiac Extracellular Matrix Constructs |
title_fullStr | Pushing the Envelope in Tissue Engineering: Ex Vivo Production of Thick Vascularized Cardiac Extracellular Matrix Constructs |
title_full_unstemmed | Pushing the Envelope in Tissue Engineering: Ex Vivo Production of Thick Vascularized Cardiac Extracellular Matrix Constructs |
title_short | Pushing the Envelope in Tissue Engineering: Ex Vivo Production of Thick Vascularized Cardiac Extracellular Matrix Constructs |
title_sort | pushing the envelope in tissue engineering: ex vivo production of thick vascularized cardiac extracellular matrix constructs |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4426298/ https://www.ncbi.nlm.nih.gov/pubmed/25602926 http://dx.doi.org/10.1089/ten.tea.2014.0477 |
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