Guided vascularization in the rat heart leads to transient vessel patterning

Recent progress in the production and maturation of iPSC-cardiomyocytes has facilitated major advances in building bioartificial heart tissue with functional cardiomyocytes. Despite this progress, vascularizing these constructs continues to be a barrier to clinical application. One emerging strategy...

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Main Authors: Eileen L. Brady, Mitchell A. Kirby, Emily Olszewski, Parker Grosjean, Fredrik Johansson, Jennifer Davis, Ruikang K. Wang, Kelly R. Stevens
Format: Article
Language:English
Published: AIP Publishing LLC 2020-03-01
Series:APL Bioengineering
Online Access:http://dx.doi.org/10.1063/1.5122804
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spelling doaj-a52f4387753048a0b183ee2354b3699c2020-11-25T02:13:33ZengAIP Publishing LLCAPL Bioengineering2473-28772020-03-0141016105016105-1110.1063/1.5122804Guided vascularization in the rat heart leads to transient vessel patterningEileen L. Brady0Mitchell A. Kirby1Emily Olszewski2Parker Grosjean3Fredrik Johansson4Jennifer Davis5Ruikang K. Wang6Kelly R. Stevens7 Department of Bioengineering, University of Washington, Seattle, Washington 98195, USA Department of Bioengineering, University of Washington, Seattle, Washington 98195, USA Department of Bioengineering, University of Washington, Seattle, Washington 98195, USA Department of Bioengineering, University of Washington, Seattle, Washington 98195, USA Department of Bioengineering, University of Washington, Seattle, Washington 98195, USA Department of Bioengineering, University of Washington, Seattle, Washington 98195, USA Department of Bioengineering, University of Washington, Seattle, Washington 98195, USA Department of Bioengineering, University of Washington, Seattle, Washington 98195, USARecent progress in the production and maturation of iPSC-cardiomyocytes has facilitated major advances in building bioartificial heart tissue with functional cardiomyocytes. Despite this progress, vascularizing these constructs continues to be a barrier to clinical application. One emerging strategy for vascularization uses aligned “cords” of endothelial cells in tissue grafts to guide assembly of chimeric microvessels upon graft implantation. Here, we test whether this approach can guide vascularization of a bioartificial tissue implanted on the rat heart. We find that patterned cords of human endothelial cells anastomose and become perfused with host blood by 3 days post-implantation. Immunohistochemical staining confirmed that graft-derived micro-vessels persist in the patch for 7 days. Furthermore, we noted a shift in distribution of vessels in the patch from patterned cord-associated clustering at 3 days to a more diffuse distribution pattern at 7 days. This loss of patterning corresponded to an infiltration of CD68+ cells and an increase in collagen within the patch. Upon further engraftment of patches containing both cords and human cardiomyocytes, we identified human cardiomyocytes and graft derived vasculature at the time of explant. Our findings show that patterned endothelial cords guide transient vessel patterning on the rat heart. Our results also suggest that future work should be directed at further adapting vascularization strategies to the epicardial environment and add to an important emerging dialog in cardiac cell therapy that points to the need to characterize host response prior to or in parallel with efficacy studies.http://dx.doi.org/10.1063/1.5122804
collection DOAJ
language English
format Article
sources DOAJ
author Eileen L. Brady
Mitchell A. Kirby
Emily Olszewski
Parker Grosjean
Fredrik Johansson
Jennifer Davis
Ruikang K. Wang
Kelly R. Stevens
spellingShingle Eileen L. Brady
Mitchell A. Kirby
Emily Olszewski
Parker Grosjean
Fredrik Johansson
Jennifer Davis
Ruikang K. Wang
Kelly R. Stevens
Guided vascularization in the rat heart leads to transient vessel patterning
APL Bioengineering
author_facet Eileen L. Brady
Mitchell A. Kirby
Emily Olszewski
Parker Grosjean
Fredrik Johansson
Jennifer Davis
Ruikang K. Wang
Kelly R. Stevens
author_sort Eileen L. Brady
title Guided vascularization in the rat heart leads to transient vessel patterning
title_short Guided vascularization in the rat heart leads to transient vessel patterning
title_full Guided vascularization in the rat heart leads to transient vessel patterning
title_fullStr Guided vascularization in the rat heart leads to transient vessel patterning
title_full_unstemmed Guided vascularization in the rat heart leads to transient vessel patterning
title_sort guided vascularization in the rat heart leads to transient vessel patterning
publisher AIP Publishing LLC
series APL Bioengineering
issn 2473-2877
publishDate 2020-03-01
description Recent progress in the production and maturation of iPSC-cardiomyocytes has facilitated major advances in building bioartificial heart tissue with functional cardiomyocytes. Despite this progress, vascularizing these constructs continues to be a barrier to clinical application. One emerging strategy for vascularization uses aligned “cords” of endothelial cells in tissue grafts to guide assembly of chimeric microvessels upon graft implantation. Here, we test whether this approach can guide vascularization of a bioartificial tissue implanted on the rat heart. We find that patterned cords of human endothelial cells anastomose and become perfused with host blood by 3 days post-implantation. Immunohistochemical staining confirmed that graft-derived micro-vessels persist in the patch for 7 days. Furthermore, we noted a shift in distribution of vessels in the patch from patterned cord-associated clustering at 3 days to a more diffuse distribution pattern at 7 days. This loss of patterning corresponded to an infiltration of CD68+ cells and an increase in collagen within the patch. Upon further engraftment of patches containing both cords and human cardiomyocytes, we identified human cardiomyocytes and graft derived vasculature at the time of explant. Our findings show that patterned endothelial cords guide transient vessel patterning on the rat heart. Our results also suggest that future work should be directed at further adapting vascularization strategies to the epicardial environment and add to an important emerging dialog in cardiac cell therapy that points to the need to characterize host response prior to or in parallel with efficacy studies.
url http://dx.doi.org/10.1063/1.5122804
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