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    A Device to Study the Effects of Stretch Gradients on Cell Behavior

    Source: Journal of Biomechanical Engineering:;2011:;volume( 133 ):;issue: 010::page 101008
    Author:
    William J. Richardson
    ,
    Richard P. Metz
    ,
    Michael R. Moreno
    ,
    Emily Wilson
    ,
    James E. Moore
    DOI: 10.1115/1.4005251
    Publisher: The American Society of Mechanical Engineers (ASME)
    Abstract: Mechanical forces are key regulators of cell function with varying loads capable of modulating behaviors such as alignment, migration, phenotype modulation, and others. Historically, cell-stretching experiments have employed mechanically simple environments (e.g., uniform uniaxial or equibiaxial stretches). However, stretch distributions in vivo can be highly non-uniform, particularly in cases of disease or subsequent to interventional treatments. Herein, we present a cell-stretching device capable of subjecting cells to controllable gradients in biaxial stretch via radial deformation of circular elastomeric membranes. By including either a defect or a rigid fixation at the center of the membrane, various gradients are generated. Capabilities of the device were quantified by tracking marked positions of the membrane while applying various loads, and experimental feasibility was assessed by conducting preliminary experiments with 3T3 fibroblasts and 10T1/2 cells subjected to 24 h of cyclic stretch. Quantitative real-time PCR was used to measure changes in mRNA expression of a profile of genes representing the major smooth muscle phenotypes. Genes associated with the contractile state were both upregulated (e.g., calponin) and downregulated (e.g., α-2-actin), and genes associated with the synthetic state were likewise both upregulated (e.g., SKI-like oncogene) and downregulated (e.g., collagen III). In addition, cells aligned with an orientation perpendicular to the maximal stretch direction. We have developed an in vitro cell culture device that can produce non-uniform stretch environments similar to in vivo mechanics. Cells stretched with this device showed alignment and altered mRNA expression indicative of phenotype modulation. Understanding these processes as they relate to in vivo pathologies could enable a more accurately targeted treatment to heal or inhibit disease, either through implantable device design or pharmaceutical approaches.
    keyword(s): Stress , Gradients , Membranes , Fibroblasts , Design , Deformation , Diseases AND Imaging ,
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      A Device to Study the Effects of Stretch Gradients on Cell Behavior

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    http://yetl.yabesh.ir/yetl1/handle/yetl/145369
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    contributor authorWilliam J. Richardson
    contributor authorRichard P. Metz
    contributor authorMichael R. Moreno
    contributor authorEmily Wilson
    contributor authorJames E. Moore
    date accessioned2017-05-09T00:42:20Z
    date available2017-05-09T00:42:20Z
    date copyrightOctober, 2011
    date issued2011
    identifier issn0148-0731
    identifier otherJBENDY-27223#101008_1.pdf
    identifier urihttp://yetl.yabesh.ir/yetl/handle/yetl/145369
    description abstractMechanical forces are key regulators of cell function with varying loads capable of modulating behaviors such as alignment, migration, phenotype modulation, and others. Historically, cell-stretching experiments have employed mechanically simple environments (e.g., uniform uniaxial or equibiaxial stretches). However, stretch distributions in vivo can be highly non-uniform, particularly in cases of disease or subsequent to interventional treatments. Herein, we present a cell-stretching device capable of subjecting cells to controllable gradients in biaxial stretch via radial deformation of circular elastomeric membranes. By including either a defect or a rigid fixation at the center of the membrane, various gradients are generated. Capabilities of the device were quantified by tracking marked positions of the membrane while applying various loads, and experimental feasibility was assessed by conducting preliminary experiments with 3T3 fibroblasts and 10T1/2 cells subjected to 24 h of cyclic stretch. Quantitative real-time PCR was used to measure changes in mRNA expression of a profile of genes representing the major smooth muscle phenotypes. Genes associated with the contractile state were both upregulated (e.g., calponin) and downregulated (e.g., α-2-actin), and genes associated with the synthetic state were likewise both upregulated (e.g., SKI-like oncogene) and downregulated (e.g., collagen III). In addition, cells aligned with an orientation perpendicular to the maximal stretch direction. We have developed an in vitro cell culture device that can produce non-uniform stretch environments similar to in vivo mechanics. Cells stretched with this device showed alignment and altered mRNA expression indicative of phenotype modulation. Understanding these processes as they relate to in vivo pathologies could enable a more accurately targeted treatment to heal or inhibit disease, either through implantable device design or pharmaceutical approaches.
    publisherThe American Society of Mechanical Engineers (ASME)
    titleA Device to Study the Effects of Stretch Gradients on Cell Behavior
    typeJournal Paper
    journal volume133
    journal issue10
    journal titleJournal of Biomechanical Engineering
    identifier doi10.1115/1.4005251
    journal fristpage101008
    identifier eissn1528-8951
    keywordsStress
    keywordsGradients
    keywordsMembranes
    keywordsFibroblasts
    keywordsDesign
    keywordsDeformation
    keywordsDiseases AND Imaging
    treeJournal of Biomechanical Engineering:;2011:;volume( 133 ):;issue: 010
    contenttypeFulltext
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    DSpace software copyright © 2002-2015  DuraSpace
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