Pushing the envelope in tissue engineering : ex vivo production of thick vascularized cardiac ECM 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'...
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sg-ntu-dr.10356-1046532023-07-14T15:52:51Z Pushing the envelope in tissue engineering : ex vivo production of thick vascularized cardiac ECM constructs Venkatraman, Subbu S. Machluf, Marcelle 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 School of Materials Science & Engineering DRNTU::Science::Medicine::Tissue engineering 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. Published version 2015-06-17T01:49:43Z 2019-12-06T21:37:00Z 2015-06-17T01:49:43Z 2019-12-06T21:37:00Z 2015 2015 Journal Article Sarig, U., Nguyen, E. B.-V., Wang, Y., Ting, S., Bronshtein, T., Sarig, H, et al. (2015). Pushing the envelope in tissue engineering: ex vivo production of thick vascularized cardiac ECM constructs. Tissue engineering Part A, 21(9-10), 1507-1519. https://hdl.handle.net/10356/104653 http://hdl.handle.net/10220/25922 10.1089/ten.tea.2014.0477 25602926 187197 en Tissue engineering Part A © 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. application/pdf |
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DRNTU::Science::Medicine::Tissue engineering Venkatraman, Subbu S. Machluf, Marcelle 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 Pushing the envelope in tissue engineering : ex vivo production of thick vascularized cardiac ECM constructs |
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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. |
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School of Materials Science & Engineering |
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School of Materials Science & Engineering Venkatraman, Subbu S. Machluf, Marcelle 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 |
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Article |
author |
Venkatraman, Subbu S. Machluf, Marcelle 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 |
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Venkatraman, Subbu S. |
title |
Pushing the envelope in tissue engineering : ex vivo production of thick vascularized cardiac ECM constructs |
title_short |
Pushing the envelope in tissue engineering : ex vivo production of thick vascularized cardiac ECM constructs |
title_full |
Pushing the envelope in tissue engineering : ex vivo production of thick vascularized cardiac ECM constructs |
title_fullStr |
Pushing the envelope in tissue engineering : ex vivo production of thick vascularized cardiac ECM constructs |
title_full_unstemmed |
Pushing the envelope in tissue engineering : ex vivo production of thick vascularized cardiac ECM constructs |
title_sort |
pushing the envelope in tissue engineering : ex vivo production of thick vascularized cardiac ecm constructs |
publishDate |
2015 |
url |
https://hdl.handle.net/10356/104653 http://hdl.handle.net/10220/25922 |
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1772827417473187840 |