Contractile Smooth Muscle and Active Stress Generation in Porcine Common CarotidsSource: Journal of Biomechanical Engineering:;2018:;volume( 140 ):;issue: 001::page 14501Author:Zhou, Boran
,
Prim, David A.
,
Romito, Eva J.
,
McNamara, Liam P.
,
Spinale, Francis G.
,
Shazly, Tarek
,
Eberth, John F.
DOI: 10.1115/1.4037949Publisher: The American Society of Mechanical Engineers (ASME)
Abstract: The mechanical response of intact blood vessels to applied loads can be delineated into passive and active components using an isometric decomposition approach. Whereas the passive response is due predominantly to the extracellular matrix (ECM) proteins and amorphous ground substance, the active response depends on the presence of smooth muscle cells (SMCs) and the contractile machinery activated within those cells. To better understand determinants of active stress generation within the vascular wall, we subjected porcine common carotid arteries (CCAs) to biaxial inflation–extension testing under maximally contracted or passive SMC conditions and semiquantitatively measured two known markers of the contractile SMC phenotype: smoothelin and smooth muscle-myosin heavy chain (SM-MHC). Using isometric decomposition and established constitutive models, an intuitive but novel correlation between the magnitude of active stress generation and the relative abundance of smoothelin and SM-MHC emerged. Our results reiterate the importance of stretch-dependent active stress generation to the total mechanical response. Overall these findings can be used to decouple the mechanical contribution of SMCs from the ECM and is therefore a powerful tool in the analysis of disease states and potential therapies where both constituent are altered.
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contributor author | Zhou, Boran | |
contributor author | Prim, David A. | |
contributor author | Romito, Eva J. | |
contributor author | McNamara, Liam P. | |
contributor author | Spinale, Francis G. | |
contributor author | Shazly, Tarek | |
contributor author | Eberth, John F. | |
date accessioned | 2019-02-28T11:11:30Z | |
date available | 2019-02-28T11:11:30Z | |
date copyright | 11/9/2017 12:00:00 AM | |
date issued | 2018 | |
identifier issn | 0148-0731 | |
identifier other | bio_140_01_014501.pdf | |
identifier uri | http://yetl.yabesh.ir/yetl1/handle/yetl/4253648 | |
description abstract | The mechanical response of intact blood vessels to applied loads can be delineated into passive and active components using an isometric decomposition approach. Whereas the passive response is due predominantly to the extracellular matrix (ECM) proteins and amorphous ground substance, the active response depends on the presence of smooth muscle cells (SMCs) and the contractile machinery activated within those cells. To better understand determinants of active stress generation within the vascular wall, we subjected porcine common carotid arteries (CCAs) to biaxial inflation–extension testing under maximally contracted or passive SMC conditions and semiquantitatively measured two known markers of the contractile SMC phenotype: smoothelin and smooth muscle-myosin heavy chain (SM-MHC). Using isometric decomposition and established constitutive models, an intuitive but novel correlation between the magnitude of active stress generation and the relative abundance of smoothelin and SM-MHC emerged. Our results reiterate the importance of stretch-dependent active stress generation to the total mechanical response. Overall these findings can be used to decouple the mechanical contribution of SMCs from the ECM and is therefore a powerful tool in the analysis of disease states and potential therapies where both constituent are altered. | |
publisher | The American Society of Mechanical Engineers (ASME) | |
title | Contractile Smooth Muscle and Active Stress Generation in Porcine Common Carotids | |
type | Journal Paper | |
journal volume | 140 | |
journal issue | 1 | |
journal title | Journal of Biomechanical Engineering | |
identifier doi | 10.1115/1.4037949 | |
journal fristpage | 14501 | |
journal lastpage | 014501-6 | |
tree | Journal of Biomechanical Engineering:;2018:;volume( 140 ):;issue: 001 | |
contenttype | Fulltext |