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De Novo Valve Tissue Morphology Following Bioscaffold Mitral Valve Replacement in a Juvenile Non-Human Primate Model
The utility of implanting a bioscaffold mitral valve consisting of porcine small intestinal submucosa (PSIS) in a juvenile baboon model (12 to 14 months old at the time of implant; n = 3) to assess their in vivo tissue remodeling responses was investigated. Our findings demonstrated that the PSIS mi...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8301182/ https://www.ncbi.nlm.nih.gov/pubmed/34356207 http://dx.doi.org/10.3390/bioengineering8070100 |
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author | Gonzalez, Brittany A. Perez Gonzalez, Marcos Scholl, Frank Bibevski, Steven Ladich, Elena Bibevski, Jennifer Morales, Pablo Lopez, Jesus Casares, Mike Brehier, Vincent Hernandez, Lazaro Ramaswamy, Sharan |
author_facet | Gonzalez, Brittany A. Perez Gonzalez, Marcos Scholl, Frank Bibevski, Steven Ladich, Elena Bibevski, Jennifer Morales, Pablo Lopez, Jesus Casares, Mike Brehier, Vincent Hernandez, Lazaro Ramaswamy, Sharan |
author_sort | Gonzalez, Brittany A. |
collection | PubMed |
description | The utility of implanting a bioscaffold mitral valve consisting of porcine small intestinal submucosa (PSIS) in a juvenile baboon model (12 to 14 months old at the time of implant; n = 3) to assess their in vivo tissue remodeling responses was investigated. Our findings demonstrated that the PSIS mitral valve exhibited the robust presence of de novo extracellular matrix (ECM) at all explantation time points (at 3-, 11-, and 20-months). Apart from a significantly lower level of proteoglycans in the implanted valve’s annulus region (p < 0.05) at 3 months compared to the 11- and 20-month explants, there were no other significant differences (p > 0.05) found between any of the other principal valve ECM components (collagen and elastin) at the leaflet, annulus, or chordae tendinea locations, across these time points. In particular, neochordae tissue had formed, which seamlessly integrated with the native papillary muscles. However, additional processing will be required to trigger accelerated, uniform and complete valve ECM formation in the recipient. Regardless of the specific processing done to the bioscaffold valve, in this proof-of-concept study, we estimate that a 3-month window following bioscaffold valve replacement is the timeline in which complete regeneration of the valve and integration with the host needs to occur. |
format | Online Article Text |
id | pubmed-8301182 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-83011822021-07-24 De Novo Valve Tissue Morphology Following Bioscaffold Mitral Valve Replacement in a Juvenile Non-Human Primate Model Gonzalez, Brittany A. Perez Gonzalez, Marcos Scholl, Frank Bibevski, Steven Ladich, Elena Bibevski, Jennifer Morales, Pablo Lopez, Jesus Casares, Mike Brehier, Vincent Hernandez, Lazaro Ramaswamy, Sharan Bioengineering (Basel) Article The utility of implanting a bioscaffold mitral valve consisting of porcine small intestinal submucosa (PSIS) in a juvenile baboon model (12 to 14 months old at the time of implant; n = 3) to assess their in vivo tissue remodeling responses was investigated. Our findings demonstrated that the PSIS mitral valve exhibited the robust presence of de novo extracellular matrix (ECM) at all explantation time points (at 3-, 11-, and 20-months). Apart from a significantly lower level of proteoglycans in the implanted valve’s annulus region (p < 0.05) at 3 months compared to the 11- and 20-month explants, there were no other significant differences (p > 0.05) found between any of the other principal valve ECM components (collagen and elastin) at the leaflet, annulus, or chordae tendinea locations, across these time points. In particular, neochordae tissue had formed, which seamlessly integrated with the native papillary muscles. However, additional processing will be required to trigger accelerated, uniform and complete valve ECM formation in the recipient. Regardless of the specific processing done to the bioscaffold valve, in this proof-of-concept study, we estimate that a 3-month window following bioscaffold valve replacement is the timeline in which complete regeneration of the valve and integration with the host needs to occur. MDPI 2021-07-16 /pmc/articles/PMC8301182/ /pubmed/34356207 http://dx.doi.org/10.3390/bioengineering8070100 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Gonzalez, Brittany A. Perez Gonzalez, Marcos Scholl, Frank Bibevski, Steven Ladich, Elena Bibevski, Jennifer Morales, Pablo Lopez, Jesus Casares, Mike Brehier, Vincent Hernandez, Lazaro Ramaswamy, Sharan De Novo Valve Tissue Morphology Following Bioscaffold Mitral Valve Replacement in a Juvenile Non-Human Primate Model |
title | De Novo Valve Tissue Morphology Following Bioscaffold Mitral Valve Replacement in a Juvenile Non-Human Primate Model |
title_full | De Novo Valve Tissue Morphology Following Bioscaffold Mitral Valve Replacement in a Juvenile Non-Human Primate Model |
title_fullStr | De Novo Valve Tissue Morphology Following Bioscaffold Mitral Valve Replacement in a Juvenile Non-Human Primate Model |
title_full_unstemmed | De Novo Valve Tissue Morphology Following Bioscaffold Mitral Valve Replacement in a Juvenile Non-Human Primate Model |
title_short | De Novo Valve Tissue Morphology Following Bioscaffold Mitral Valve Replacement in a Juvenile Non-Human Primate Model |
title_sort | de novo valve tissue morphology following bioscaffold mitral valve replacement in a juvenile non-human primate model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8301182/ https://www.ncbi.nlm.nih.gov/pubmed/34356207 http://dx.doi.org/10.3390/bioengineering8070100 |
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