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Pigmentation Affects Elastic Fiber Patterning and Biomechanical Behavior of the Murine Aortic Valve
The aortic valve (AoV) maintains unidirectional blood distribution from the left ventricle of the heart to the aorta for systemic circulation. The AoV leaflets rely on a precise extracellular matrix microarchitecture of collagen, elastin, and proteoglycans for appropriate biomechanical performance....
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8702816/ https://www.ncbi.nlm.nih.gov/pubmed/34957247 http://dx.doi.org/10.3389/fcvm.2021.754560 |
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author | Nasim, Sana Pandey, Popular Kanashiro-Takeuchi, Rosemeire M. He, Jin Hutcheson, Joshua D. Kos, Lidia |
author_facet | Nasim, Sana Pandey, Popular Kanashiro-Takeuchi, Rosemeire M. He, Jin Hutcheson, Joshua D. Kos, Lidia |
author_sort | Nasim, Sana |
collection | PubMed |
description | The aortic valve (AoV) maintains unidirectional blood distribution from the left ventricle of the heart to the aorta for systemic circulation. The AoV leaflets rely on a precise extracellular matrix microarchitecture of collagen, elastin, and proteoglycans for appropriate biomechanical performance. We have previously demonstrated a relationship between the presence of pigment in the mouse AoV with elastic fiber patterning using multiphoton imaging. Here, we extended those findings using wholemount confocal microscopy revealing that elastic fibers were diminished in the AoV of hypopigmented mice (Kit(Wv) and albino) and were disorganized in the AoV of K5-Edn3 transgenic hyperpigmented mice when compared to wild type C57BL/6J mice. We further used atomic force microscopy to measure stiffness differences in the wholemount AoV leaflets of mice with different levels of pigmentation. We show that AoV leaflets of K5-Edn3 had overall higher stiffness (4.42 ± 0.35 kPa) when compared to those from Kit(Wv) (2.22 ± 0.21 kPa), albino (2.45 ± 0.16 kPa), and C57BL/6J (3.0 ± 0.16 kPa) mice. Despite the striking elastic fiber phenotype and noted stiffness differences, adult mutant mice were found to have no overt cardiac differences as measured by echocardiography. Our results indicate that pigmentation, but not melanocytes, is required for proper elastic fiber organization in the mouse AoV and dictates its biomechanical properties. |
format | Online Article Text |
id | pubmed-8702816 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-87028162021-12-25 Pigmentation Affects Elastic Fiber Patterning and Biomechanical Behavior of the Murine Aortic Valve Nasim, Sana Pandey, Popular Kanashiro-Takeuchi, Rosemeire M. He, Jin Hutcheson, Joshua D. Kos, Lidia Front Cardiovasc Med Cardiovascular Medicine The aortic valve (AoV) maintains unidirectional blood distribution from the left ventricle of the heart to the aorta for systemic circulation. The AoV leaflets rely on a precise extracellular matrix microarchitecture of collagen, elastin, and proteoglycans for appropriate biomechanical performance. We have previously demonstrated a relationship between the presence of pigment in the mouse AoV with elastic fiber patterning using multiphoton imaging. Here, we extended those findings using wholemount confocal microscopy revealing that elastic fibers were diminished in the AoV of hypopigmented mice (Kit(Wv) and albino) and were disorganized in the AoV of K5-Edn3 transgenic hyperpigmented mice when compared to wild type C57BL/6J mice. We further used atomic force microscopy to measure stiffness differences in the wholemount AoV leaflets of mice with different levels of pigmentation. We show that AoV leaflets of K5-Edn3 had overall higher stiffness (4.42 ± 0.35 kPa) when compared to those from Kit(Wv) (2.22 ± 0.21 kPa), albino (2.45 ± 0.16 kPa), and C57BL/6J (3.0 ± 0.16 kPa) mice. Despite the striking elastic fiber phenotype and noted stiffness differences, adult mutant mice were found to have no overt cardiac differences as measured by echocardiography. Our results indicate that pigmentation, but not melanocytes, is required for proper elastic fiber organization in the mouse AoV and dictates its biomechanical properties. Frontiers Media S.A. 2021-12-10 /pmc/articles/PMC8702816/ /pubmed/34957247 http://dx.doi.org/10.3389/fcvm.2021.754560 Text en Copyright © 2021 Nasim, Pandey, Kanashiro-Takeuchi, He, Hutcheson and Kos. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cardiovascular Medicine Nasim, Sana Pandey, Popular Kanashiro-Takeuchi, Rosemeire M. He, Jin Hutcheson, Joshua D. Kos, Lidia Pigmentation Affects Elastic Fiber Patterning and Biomechanical Behavior of the Murine Aortic Valve |
title | Pigmentation Affects Elastic Fiber Patterning and Biomechanical Behavior of the Murine Aortic Valve |
title_full | Pigmentation Affects Elastic Fiber Patterning and Biomechanical Behavior of the Murine Aortic Valve |
title_fullStr | Pigmentation Affects Elastic Fiber Patterning and Biomechanical Behavior of the Murine Aortic Valve |
title_full_unstemmed | Pigmentation Affects Elastic Fiber Patterning and Biomechanical Behavior of the Murine Aortic Valve |
title_short | Pigmentation Affects Elastic Fiber Patterning and Biomechanical Behavior of the Murine Aortic Valve |
title_sort | pigmentation affects elastic fiber patterning and biomechanical behavior of the murine aortic valve |
topic | Cardiovascular Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8702816/ https://www.ncbi.nlm.nih.gov/pubmed/34957247 http://dx.doi.org/10.3389/fcvm.2021.754560 |
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