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    Applying Physiologically Relevant Strains to Tenocytes in an In Vitro Cell Device Induces In Vivo Like Behaviors

    Source: Journal of Biomechanical Engineering:;2016:;volume( 138 ):;issue: 012::page 121003
    Author:
    Joo Kim, Jung
    ,
    Musson, David S.
    ,
    Matthews, Brya G.
    ,
    Cornish, Jillian
    ,
    Anderson, Iain A.
    ,
    Shim, Vickie B.
    DOI: 10.1115/1.4034031
    Publisher: The American Society of Mechanical Engineers (ASME)
    Abstract: We have developed a novel cell stretching device (called Cell Gym) capable of applying physiologically relevant low magnitude strains to tenocytes on a collagen type I coated membrane. We validated our device thoroughly on two levels: (1) substrate strains, (2) cell level strains. Our cell level strain results showed that the applied stretches were transferred to cells accurately (∼90%). Our gene expression data showed that mechanically stimulated tenocytes (4%) expressed a lower level of COL I gene. COX2 gene was increased but did not reach statistical significance. Our device was then tested to see if it could reproduce results from an in vivo study that measured time-dependent changes in collagen synthesis. Our results showed that collagen synthesis peaked at 24 hrs after exercise and then decreased, which matched the results from the in vivo study. Our study demonstrated that it is important to incorporate physiologically relevant low strain magnitudes in in vitro cell mechanical studies and the need to validate the device thoroughly to operate the device at small strains. This device will be used in designing novel tendon tissue engineering scaffolds in the future.
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      Applying Physiologically Relevant Strains to Tenocytes in an In Vitro Cell Device Induces In Vivo Like Behaviors

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    http://yetl.yabesh.ir/yetl1/handle/yetl/4234875
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    • Journal of Biomechanical Engineering

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    contributor authorJoo Kim, Jung
    contributor authorMusson, David S.
    contributor authorMatthews, Brya G.
    contributor authorCornish, Jillian
    contributor authorAnderson, Iain A.
    contributor authorShim, Vickie B.
    date accessioned2017-11-25T07:17:58Z
    date available2017-11-25T07:17:58Z
    date copyright2016/11/03
    date issued2016
    identifier issn0148-0731
    identifier otherbio_138_12_121003.pdf
    identifier urihttp://138.201.223.254:8080/yetl1/handle/yetl/4234875
    description abstractWe have developed a novel cell stretching device (called Cell Gym) capable of applying physiologically relevant low magnitude strains to tenocytes on a collagen type I coated membrane. We validated our device thoroughly on two levels: (1) substrate strains, (2) cell level strains. Our cell level strain results showed that the applied stretches were transferred to cells accurately (∼90%). Our gene expression data showed that mechanically stimulated tenocytes (4%) expressed a lower level of COL I gene. COX2 gene was increased but did not reach statistical significance. Our device was then tested to see if it could reproduce results from an in vivo study that measured time-dependent changes in collagen synthesis. Our results showed that collagen synthesis peaked at 24 hrs after exercise and then decreased, which matched the results from the in vivo study. Our study demonstrated that it is important to incorporate physiologically relevant low strain magnitudes in in vitro cell mechanical studies and the need to validate the device thoroughly to operate the device at small strains. This device will be used in designing novel tendon tissue engineering scaffolds in the future.
    publisherThe American Society of Mechanical Engineers (ASME)
    titleApplying Physiologically Relevant Strains to Tenocytes in an In Vitro Cell Device Induces In Vivo Like Behaviors
    typeJournal Paper
    journal volume138
    journal issue12
    journal titleJournal of Biomechanical Engineering
    identifier doi10.1115/1.4034031
    journal fristpage121003
    journal lastpage121003-9
    treeJournal of Biomechanical Engineering:;2016:;volume( 138 ):;issue: 012
    contenttypeFulltext
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    DSpace software copyright © 2002-2015  DuraSpace
    نرم افزار کتابخانه دیجیتال "دی اسپیس" فارسی شده توسط یابش برای کتابخانه های ایرانی | تماس با یابش
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