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    Simulation of the Mechanical Response of Cells on Micropost Substrates

    Source: Journal of Biomechanical Engineering:;2013:;volume( 135 ):;issue: 010::page 101012
    Author:
    Ronan, William
    ,
    Pathak, Amit
    ,
    Deshpande, Vikram S.
    ,
    McMeeking, Robert M.
    ,
    McGarry, J. Patrick
    DOI: 10.1115/1.4025114
    Publisher: The American Society of Mechanical Engineers (ASME)
    Abstract: Experimental studies where cells are seeded on micropost arrays in order to quantify their contractile behavior are becoming increasingly common. Interpretation of the data generated by this experimental technique is difficult, due to the complexity of the processes underlying cellular contractility and mechanotransduction. In the current study, a coupled framework that considers strain rate dependent contractility and remodeling of the cytoskeleton is used in tandem with a thermodynamic model of tension dependent focal adhesion formation to investigate the biomechanical response of cells adhered to micropost arrays. Computational investigations of the following experimental studies are presented: cell behavior on different sized arrays with a range of post stiffness; stress fiber and focal adhesion formation in irregularly shaped cells; the response of cells to deformations applied locally to individual posts; and the response of cells to equibiaxial stretching of micropost arrays. The predicted stress fiber and focal adhesion distributions; in addition to the predicted post tractions are quantitatively and qualitatively supported by previously published experimental data. The computational models presented in this study thus provide a framework for the design and interpretation of experimental micropost studies.
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      Simulation of the Mechanical Response of Cells on Micropost Substrates

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    contributor authorRonan, William
    contributor authorPathak, Amit
    contributor authorDeshpande, Vikram S.
    contributor authorMcMeeking, Robert M.
    contributor authorMcGarry, J. Patrick
    date accessioned2017-05-09T00:56:49Z
    date available2017-05-09T00:56:49Z
    date issued2013
    identifier issn0148-0731
    identifier otherbio_135_10_101012.pdf
    identifier urihttp://yetl.yabesh.ir/yetl/handle/yetl/151107
    description abstractExperimental studies where cells are seeded on micropost arrays in order to quantify their contractile behavior are becoming increasingly common. Interpretation of the data generated by this experimental technique is difficult, due to the complexity of the processes underlying cellular contractility and mechanotransduction. In the current study, a coupled framework that considers strain rate dependent contractility and remodeling of the cytoskeleton is used in tandem with a thermodynamic model of tension dependent focal adhesion formation to investigate the biomechanical response of cells adhered to micropost arrays. Computational investigations of the following experimental studies are presented: cell behavior on different sized arrays with a range of post stiffness; stress fiber and focal adhesion formation in irregularly shaped cells; the response of cells to deformations applied locally to individual posts; and the response of cells to equibiaxial stretching of micropost arrays. The predicted stress fiber and focal adhesion distributions; in addition to the predicted post tractions are quantitatively and qualitatively supported by previously published experimental data. The computational models presented in this study thus provide a framework for the design and interpretation of experimental micropost studies.
    publisherThe American Society of Mechanical Engineers (ASME)
    titleSimulation of the Mechanical Response of Cells on Micropost Substrates
    typeJournal Paper
    journal volume135
    journal issue10
    journal titleJournal of Biomechanical Engineering
    identifier doi10.1115/1.4025114
    journal fristpage101012
    journal lastpage101012
    identifier eissn1528-8951
    treeJournal of Biomechanical Engineering:;2013:;volume( 135 ):;issue: 010
    contenttypeFulltext
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