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    In Vitro Flow Chamber Design for the Study of Endothelial Cell (Patho)Physiology

    Source: Journal of Biomechanical Engineering:;2021:;volume( 144 ):;issue: 002::page 20801-1
    Author:
    Fallon, Meghan E.
    ,
    Mathews, Rick
    ,
    Hinds, Monica T.
    DOI: 10.1115/1.4051765
    Publisher: The American Society of Mechanical Engineers (ASME)
    Abstract: In the native vasculature, flowing blood produces a frictional force on vessel walls that affects endothelial cell function and phenotype. In the arterial system, the vasculature's local geometry directly influences variations in flow profiles and shear stress magnitudes. Straight arterial sections with pulsatile shear stress have been shown to promote an athero-protective endothelial phenotype. Conversely, areas with more complex geometry, such as arterial bifurcations and branch points with disturbed flow patterns and lower, oscillatory shear stress, typically lead to endothelial dysfunction and the pathogenesis of cardiovascular diseases. Many studies have investigated the regulation of endothelial responses to various shear stress environments. Importantly, the accurate in vitro simulation of in vivo hemodynamics is critical to the deeper understanding of mechanotransduction through the proper design and use of flow chamber devices. In this review, we describe several flow chamber apparatuses and their fluid mechanics design parameters, including parallel-plate flow chambers, cone-and-plate devices, and microfluidic devices. In addition, chamber-specific design criteria and relevant equations are defined in detail for the accurate simulation of shear stress environments to study endothelial cell responses.
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      In Vitro Flow Chamber Design for the Study of Endothelial Cell (Patho)Physiology

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    https://yetl.yabesh.ir/yetl1/handle/yetl/4284819
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    • Journal of Biomechanical Engineering

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    contributor authorFallon, Meghan E.
    contributor authorMathews, Rick
    contributor authorHinds, Monica T.
    date accessioned2022-05-08T09:10:42Z
    date available2022-05-08T09:10:42Z
    date copyright10/11/2021 12:00:00 AM
    date issued2021
    identifier issn0148-0731
    identifier otherbio_144_02_020801.pdf
    identifier urihttp://yetl.yabesh.ir/yetl1/handle/yetl/4284819
    description abstractIn the native vasculature, flowing blood produces a frictional force on vessel walls that affects endothelial cell function and phenotype. In the arterial system, the vasculature's local geometry directly influences variations in flow profiles and shear stress magnitudes. Straight arterial sections with pulsatile shear stress have been shown to promote an athero-protective endothelial phenotype. Conversely, areas with more complex geometry, such as arterial bifurcations and branch points with disturbed flow patterns and lower, oscillatory shear stress, typically lead to endothelial dysfunction and the pathogenesis of cardiovascular diseases. Many studies have investigated the regulation of endothelial responses to various shear stress environments. Importantly, the accurate in vitro simulation of in vivo hemodynamics is critical to the deeper understanding of mechanotransduction through the proper design and use of flow chamber devices. In this review, we describe several flow chamber apparatuses and their fluid mechanics design parameters, including parallel-plate flow chambers, cone-and-plate devices, and microfluidic devices. In addition, chamber-specific design criteria and relevant equations are defined in detail for the accurate simulation of shear stress environments to study endothelial cell responses.
    publisherThe American Society of Mechanical Engineers (ASME)
    titleIn Vitro Flow Chamber Design for the Study of Endothelial Cell (Patho)Physiology
    typeJournal Paper
    journal volume144
    journal issue2
    journal titleJournal of Biomechanical Engineering
    identifier doi10.1115/1.4051765
    journal fristpage20801-1
    journal lastpage20801-21
    page21
    treeJournal of Biomechanical Engineering:;2021:;volume( 144 ):;issue: 002
    contenttypeFulltext
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    DSpace software copyright © 2002-2015  DuraSpace
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