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Patterned human microvascular grafts enable rapid vascularization and increase perfusion in infarcted rat hearts
Vascularization and efficient perfusion are long-standing challenges in cardiac tissue engineering. Here we report engineered perfusable microvascular constructs, wherein human embryonic stem cell-derived endothelial cells (hESC-ECs) are seeded both into patterned microchannels and the surrounding c...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6362250/ https://www.ncbi.nlm.nih.gov/pubmed/30718840 http://dx.doi.org/10.1038/s41467-019-08388-7 |
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author | Redd, Meredith A. Zeinstra, Nicole Qin, Wan Wei, Wei Martinson, Amy Wang, Yuliang Wang, Ruikang K. Murry, Charles E. Zheng, Ying |
author_facet | Redd, Meredith A. Zeinstra, Nicole Qin, Wan Wei, Wei Martinson, Amy Wang, Yuliang Wang, Ruikang K. Murry, Charles E. Zheng, Ying |
author_sort | Redd, Meredith A. |
collection | PubMed |
description | Vascularization and efficient perfusion are long-standing challenges in cardiac tissue engineering. Here we report engineered perfusable microvascular constructs, wherein human embryonic stem cell-derived endothelial cells (hESC-ECs) are seeded both into patterned microchannels and the surrounding collagen matrix. In vitro, the hESC-ECs lining the luminal walls readily sprout and anastomose with de novo-formed endothelial tubes in the matrix under flow. When implanted on infarcted rat hearts, the perfusable microvessel grafts integrate with coronary vasculature to a greater degree than non-perfusable self-assembled constructs at 5 days post-implantation. Optical microangiography imaging reveal that perfusable grafts have 6-fold greater vascular density, 2.5-fold higher vascular velocities and >20-fold higher volumetric perfusion rates. Implantation of perfusable grafts containing additional hESC-derived cardiomyocytes show higher cardiomyocyte and vascular density. Thus, pre-patterned vascular networks enhance vascular remodeling and accelerate coronary perfusion, potentially supporting cardiac tissues after implantation. These findings should facilitate the next generation of cardiac tissue engineering design. |
format | Online Article Text |
id | pubmed-6362250 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63622502019-02-06 Patterned human microvascular grafts enable rapid vascularization and increase perfusion in infarcted rat hearts Redd, Meredith A. Zeinstra, Nicole Qin, Wan Wei, Wei Martinson, Amy Wang, Yuliang Wang, Ruikang K. Murry, Charles E. Zheng, Ying Nat Commun Article Vascularization and efficient perfusion are long-standing challenges in cardiac tissue engineering. Here we report engineered perfusable microvascular constructs, wherein human embryonic stem cell-derived endothelial cells (hESC-ECs) are seeded both into patterned microchannels and the surrounding collagen matrix. In vitro, the hESC-ECs lining the luminal walls readily sprout and anastomose with de novo-formed endothelial tubes in the matrix under flow. When implanted on infarcted rat hearts, the perfusable microvessel grafts integrate with coronary vasculature to a greater degree than non-perfusable self-assembled constructs at 5 days post-implantation. Optical microangiography imaging reveal that perfusable grafts have 6-fold greater vascular density, 2.5-fold higher vascular velocities and >20-fold higher volumetric perfusion rates. Implantation of perfusable grafts containing additional hESC-derived cardiomyocytes show higher cardiomyocyte and vascular density. Thus, pre-patterned vascular networks enhance vascular remodeling and accelerate coronary perfusion, potentially supporting cardiac tissues after implantation. These findings should facilitate the next generation of cardiac tissue engineering design. Nature Publishing Group UK 2019-02-04 /pmc/articles/PMC6362250/ /pubmed/30718840 http://dx.doi.org/10.1038/s41467-019-08388-7 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Redd, Meredith A. Zeinstra, Nicole Qin, Wan Wei, Wei Martinson, Amy Wang, Yuliang Wang, Ruikang K. Murry, Charles E. Zheng, Ying Patterned human microvascular grafts enable rapid vascularization and increase perfusion in infarcted rat hearts |
title | Patterned human microvascular grafts enable rapid vascularization and increase perfusion in infarcted rat hearts |
title_full | Patterned human microvascular grafts enable rapid vascularization and increase perfusion in infarcted rat hearts |
title_fullStr | Patterned human microvascular grafts enable rapid vascularization and increase perfusion in infarcted rat hearts |
title_full_unstemmed | Patterned human microvascular grafts enable rapid vascularization and increase perfusion in infarcted rat hearts |
title_short | Patterned human microvascular grafts enable rapid vascularization and increase perfusion in infarcted rat hearts |
title_sort | patterned human microvascular grafts enable rapid vascularization and increase perfusion in infarcted rat hearts |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6362250/ https://www.ncbi.nlm.nih.gov/pubmed/30718840 http://dx.doi.org/10.1038/s41467-019-08388-7 |
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