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On the shape and structure of the murine pulmonary heart valve
Murine animal models are an established standard in translational research and provides a potential platform for studying heart valve disease. To date, studies on heart valve disease using murine models have been hindered by a lack of appropriate methodologies due to their small scale. In the presen...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8263753/ https://www.ncbi.nlm.nih.gov/pubmed/34234231 http://dx.doi.org/10.1038/s41598-021-93513-0 |
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author | Liu, Yifei Feng, Xinzeng Liu, Hao McComb, David W. Breuer, Christopher K. Sacks, Michael S. |
author_facet | Liu, Yifei Feng, Xinzeng Liu, Hao McComb, David W. Breuer, Christopher K. Sacks, Michael S. |
author_sort | Liu, Yifei |
collection | PubMed |
description | Murine animal models are an established standard in translational research and provides a potential platform for studying heart valve disease. To date, studies on heart valve disease using murine models have been hindered by a lack of appropriate methodologies due to their small scale. In the present study, we developed a multi-scale, imaging-based approach to extract the functional structure and geometry for the murine heart valve. We chose the pulmonary valve (PV) to study, due to its importance in congenital heart valve disease. Excised pulmonary outflow tracts from eleven 1-year old C57BL/6J mice were fixed at 10, 20, and 30 mmHg to simulate physiological loading. Micro-computed tomography was used to reconstruct the 3D organ-level PV geometry, which was then spatially correlated with serial en-face scanning electron microscopy imaging to quantify local collagen fiber distributions. From the acquired volume renderings, we obtained the geometric descriptors of the murine PV under increasing transvalvular pressures, which demonstrated remarkable consistency. Results to date suggest that the preferred collagen orientation was predominantly in the circumferential direction, as in larger mammalian valves. The present study represents a first step in establishing organ-level murine models for the study of heart valve disease. |
format | Online Article Text |
id | pubmed-8263753 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-82637532021-07-09 On the shape and structure of the murine pulmonary heart valve Liu, Yifei Feng, Xinzeng Liu, Hao McComb, David W. Breuer, Christopher K. Sacks, Michael S. Sci Rep Article Murine animal models are an established standard in translational research and provides a potential platform for studying heart valve disease. To date, studies on heart valve disease using murine models have been hindered by a lack of appropriate methodologies due to their small scale. In the present study, we developed a multi-scale, imaging-based approach to extract the functional structure and geometry for the murine heart valve. We chose the pulmonary valve (PV) to study, due to its importance in congenital heart valve disease. Excised pulmonary outflow tracts from eleven 1-year old C57BL/6J mice were fixed at 10, 20, and 30 mmHg to simulate physiological loading. Micro-computed tomography was used to reconstruct the 3D organ-level PV geometry, which was then spatially correlated with serial en-face scanning electron microscopy imaging to quantify local collagen fiber distributions. From the acquired volume renderings, we obtained the geometric descriptors of the murine PV under increasing transvalvular pressures, which demonstrated remarkable consistency. Results to date suggest that the preferred collagen orientation was predominantly in the circumferential direction, as in larger mammalian valves. The present study represents a first step in establishing organ-level murine models for the study of heart valve disease. Nature Publishing Group UK 2021-07-07 /pmc/articles/PMC8263753/ /pubmed/34234231 http://dx.doi.org/10.1038/s41598-021-93513-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Liu, Yifei Feng, Xinzeng Liu, Hao McComb, David W. Breuer, Christopher K. Sacks, Michael S. On the shape and structure of the murine pulmonary heart valve |
title | On the shape and structure of the murine pulmonary heart valve |
title_full | On the shape and structure of the murine pulmonary heart valve |
title_fullStr | On the shape and structure of the murine pulmonary heart valve |
title_full_unstemmed | On the shape and structure of the murine pulmonary heart valve |
title_short | On the shape and structure of the murine pulmonary heart valve |
title_sort | on the shape and structure of the murine pulmonary heart valve |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8263753/ https://www.ncbi.nlm.nih.gov/pubmed/34234231 http://dx.doi.org/10.1038/s41598-021-93513-0 |
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