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    Mechanical Vibration Regulates Differentiation and Proliferation of Neural Stem Cells

    Source: Journal of Engineering and Science in Medical Diagnostics and Therapy:;2025:;volume( 008 ):;issue: 003::page 31012-1
    Author:
    Shiraishi, Toshihiko
    ,
    Eguchi, Hiroaki
    ,
    Kanno, Hiroshi
    DOI: 10.1115/1.4067670
    Publisher: The American Society of Mechanical Engineers (ASME)
    Abstract: For the regeneration of the central nervous system, neural stem cells have been proposed as graft donors. Conventional studies have used biochemical factors to induce their differentiation into neurons and to enhance axon elongation. However, few studies have been reported on the effects of mechanical factors on neural stem cells. In this study, we show that mechanical vibration directs the differentiation of neural stem cells into neuronal cells, elongates their axons, and increases the number of differentiated cells. We found that the 25 Hz and 0.5 G vibration promoted the differentiation of neural stem cells into neuronal-marker-positive cells expressing neurofilament heavy polypeptide by 2.5-fold compared to the control conditions and increased the number of differentiated cells with axons longer than 10 μm by 1.5-fold at 7 days of culture. Furthermore, we found that the total number of differentiated and undifferentiated cells in the vibration condition reached 2.9-fold more than the control condition and that this effect depended on the frequency and acceleration. We anticipate our system to facilitate further studies using mechanical vibration such as regenerative therapy using neural stem cells and the elucidation of differentiation mechanisms in neural stem cells.
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      Mechanical Vibration Regulates Differentiation and Proliferation of Neural Stem Cells

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    http://yetl.yabesh.ir/yetl1/handle/yetl/4308155
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    contributor authorShiraishi, Toshihiko
    contributor authorEguchi, Hiroaki
    contributor authorKanno, Hiroshi
    date accessioned2025-08-20T09:21:51Z
    date available2025-08-20T09:21:51Z
    date copyright2/28/2025 12:00:00 AM
    date issued2025
    identifier issn2572-7958
    identifier otherjesmdt_008_03_031012.pdf
    identifier urihttp://yetl.yabesh.ir/yetl1/handle/yetl/4308155
    description abstractFor the regeneration of the central nervous system, neural stem cells have been proposed as graft donors. Conventional studies have used biochemical factors to induce their differentiation into neurons and to enhance axon elongation. However, few studies have been reported on the effects of mechanical factors on neural stem cells. In this study, we show that mechanical vibration directs the differentiation of neural stem cells into neuronal cells, elongates their axons, and increases the number of differentiated cells. We found that the 25 Hz and 0.5 G vibration promoted the differentiation of neural stem cells into neuronal-marker-positive cells expressing neurofilament heavy polypeptide by 2.5-fold compared to the control conditions and increased the number of differentiated cells with axons longer than 10 μm by 1.5-fold at 7 days of culture. Furthermore, we found that the total number of differentiated and undifferentiated cells in the vibration condition reached 2.9-fold more than the control condition and that this effect depended on the frequency and acceleration. We anticipate our system to facilitate further studies using mechanical vibration such as regenerative therapy using neural stem cells and the elucidation of differentiation mechanisms in neural stem cells.
    publisherThe American Society of Mechanical Engineers (ASME)
    titleMechanical Vibration Regulates Differentiation and Proliferation of Neural Stem Cells
    typeJournal Paper
    journal volume8
    journal issue3
    journal titleJournal of Engineering and Science in Medical Diagnostics and Therapy
    identifier doi10.1115/1.4067670
    journal fristpage31012-1
    journal lastpage31012-8
    page8
    treeJournal of Engineering and Science in Medical Diagnostics and Therapy:;2025:;volume( 008 ):;issue: 003
    contenttypeFulltext
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