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Mechanics-driven mechanobiological mechanisms of arterial tortuosity
Arterial tortuosity manifests in many conditions, including hypertension, genetic mutations predisposing to thoracic aortopathy, and vascular aging. Despite evidence that tortuosity disrupts efficient blood flow and that it may be an important clinical biomarker, underlying mechanisms remain poorly...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7821897/ https://www.ncbi.nlm.nih.gov/pubmed/33277255 http://dx.doi.org/10.1126/sciadv.abd3574 |
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author | Weiss, Dar Cavinato, Cristina Gray, Authia Ramachandra, Abhay B. Avril, Stephane Humphrey, Jay D. Latorre, Marcos |
author_facet | Weiss, Dar Cavinato, Cristina Gray, Authia Ramachandra, Abhay B. Avril, Stephane Humphrey, Jay D. Latorre, Marcos |
author_sort | Weiss, Dar |
collection | PubMed |
description | Arterial tortuosity manifests in many conditions, including hypertension, genetic mutations predisposing to thoracic aortopathy, and vascular aging. Despite evidence that tortuosity disrupts efficient blood flow and that it may be an important clinical biomarker, underlying mechanisms remain poorly understood but are widely appreciated to be largely biomechanical. Many previous studies suggested that tortuosity may arise via an elastic structural buckling instability, but the novel experimental-computational approach used here suggests that tortuosity arises from mechanosensitive, cell-mediated responses to local aberrations in the microstructural integrity of the arterial wall. In particular, computations informed by multimodality imaging show that aberrations in elastic fiber integrity, collagen alignment, and collagen turnover can lead to a progressive loss of structural stability that entrenches during the development of tortuosity. Interpreted in this way, microstructural defects or irregularities of the arterial wall initiate the condition and hypertension is a confounding factor. |
format | Online Article Text |
id | pubmed-7821897 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-78218972021-01-29 Mechanics-driven mechanobiological mechanisms of arterial tortuosity Weiss, Dar Cavinato, Cristina Gray, Authia Ramachandra, Abhay B. Avril, Stephane Humphrey, Jay D. Latorre, Marcos Sci Adv Research Articles Arterial tortuosity manifests in many conditions, including hypertension, genetic mutations predisposing to thoracic aortopathy, and vascular aging. Despite evidence that tortuosity disrupts efficient blood flow and that it may be an important clinical biomarker, underlying mechanisms remain poorly understood but are widely appreciated to be largely biomechanical. Many previous studies suggested that tortuosity may arise via an elastic structural buckling instability, but the novel experimental-computational approach used here suggests that tortuosity arises from mechanosensitive, cell-mediated responses to local aberrations in the microstructural integrity of the arterial wall. In particular, computations informed by multimodality imaging show that aberrations in elastic fiber integrity, collagen alignment, and collagen turnover can lead to a progressive loss of structural stability that entrenches during the development of tortuosity. Interpreted in this way, microstructural defects or irregularities of the arterial wall initiate the condition and hypertension is a confounding factor. American Association for the Advancement of Science 2020-12-04 /pmc/articles/PMC7821897/ /pubmed/33277255 http://dx.doi.org/10.1126/sciadv.abd3574 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/ https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Weiss, Dar Cavinato, Cristina Gray, Authia Ramachandra, Abhay B. Avril, Stephane Humphrey, Jay D. Latorre, Marcos Mechanics-driven mechanobiological mechanisms of arterial tortuosity |
title | Mechanics-driven mechanobiological mechanisms of arterial tortuosity |
title_full | Mechanics-driven mechanobiological mechanisms of arterial tortuosity |
title_fullStr | Mechanics-driven mechanobiological mechanisms of arterial tortuosity |
title_full_unstemmed | Mechanics-driven mechanobiological mechanisms of arterial tortuosity |
title_short | Mechanics-driven mechanobiological mechanisms of arterial tortuosity |
title_sort | mechanics-driven mechanobiological mechanisms of arterial tortuosity |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7821897/ https://www.ncbi.nlm.nih.gov/pubmed/33277255 http://dx.doi.org/10.1126/sciadv.abd3574 |
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