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    Development of Polymeric Nerve Guidance Conduits That Contain Anisotropic Cues Including Aligned Microfibers and Gradients of Adsorbed Laminin-1

    Source: Journal of Medical Devices:;2008:;volume( 002 ):;issue: 002::page 27524
    Author:
    Jared M. Cregg
    ,
    Han Bing Wang
    ,
    Michael E. Mullins
    ,
    Ryan J. Gilbert
    DOI: 10.1115/1.2934348
    Publisher: The American Society of Mechanical Engineers (ASME)
    Abstract: Structures that direct neurite extension are important for regeneration following spinal cord injury and peripheral nerve injury. Within the spinal cord, neurons encounter a glial scar environment that impedes regeneration. In the peripheral nervous system, endogenous regeneration cannot occur across nerve gaps greater than 2mm. Current repair strategies use guidance conduits to channel axonal growth towards distal targets. While showing promise, conduit walls do not provide a suitable environment for neuronal attachment or extension, and axonal growth within conduits remains tortuous. Hence, there is a need for development of three-dimensional (3D) structures that use contact guidance—rather than confinement—as a means of guided regeneration. Our laboratory has developed aligned, electrospun fiber matrices that have been shown to direct neurite extension in vitro. In addition, a gradient of the glycoprotein laminin-1 has been adsorbed onto aligned microfiber matrices to stimulate directional growth. These matrices were then manipulated into 3D conduit structures. Novel polymeric conduits that utilize contact guidance and contain gradients of molecules that stimulate directional growth have the potential to foster fast, directed regeneration into and through conduit structures.
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      Development of Polymeric Nerve Guidance Conduits That Contain Anisotropic Cues Including Aligned Microfibers and Gradients of Adsorbed Laminin-1

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    contributor authorJared M. Cregg
    contributor authorHan Bing Wang
    contributor authorMichael E. Mullins
    contributor authorRyan J. Gilbert
    date accessioned2017-05-09T00:29:57Z
    date available2017-05-09T00:29:57Z
    date copyrightJune, 2008
    date issued2008
    identifier issn1932-6181
    identifier otherJMDOA4-27991#027524_1.pdf
    identifier urihttp://yetl.yabesh.ir/yetl/handle/yetl/139030
    description abstractStructures that direct neurite extension are important for regeneration following spinal cord injury and peripheral nerve injury. Within the spinal cord, neurons encounter a glial scar environment that impedes regeneration. In the peripheral nervous system, endogenous regeneration cannot occur across nerve gaps greater than 2mm. Current repair strategies use guidance conduits to channel axonal growth towards distal targets. While showing promise, conduit walls do not provide a suitable environment for neuronal attachment or extension, and axonal growth within conduits remains tortuous. Hence, there is a need for development of three-dimensional (3D) structures that use contact guidance—rather than confinement—as a means of guided regeneration. Our laboratory has developed aligned, electrospun fiber matrices that have been shown to direct neurite extension in vitro. In addition, a gradient of the glycoprotein laminin-1 has been adsorbed onto aligned microfiber matrices to stimulate directional growth. These matrices were then manipulated into 3D conduit structures. Novel polymeric conduits that utilize contact guidance and contain gradients of molecules that stimulate directional growth have the potential to foster fast, directed regeneration into and through conduit structures.
    publisherThe American Society of Mechanical Engineers (ASME)
    titleDevelopment of Polymeric Nerve Guidance Conduits That Contain Anisotropic Cues Including Aligned Microfibers and Gradients of Adsorbed Laminin-1
    typeJournal Paper
    journal volume2
    journal issue2
    journal titleJournal of Medical Devices
    identifier doi10.1115/1.2934348
    journal fristpage27524
    identifier eissn1932-619X
    treeJournal of Medical Devices:;2008:;volume( 002 ):;issue: 002
    contenttypeFulltext
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