國家衛生研究院 NHRI:Item 3990099045/7916
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    Please use this identifier to cite or link to this item: http://ir.nhri.org.tw/handle/3990099045/7916


    Title: Matriptase is required for the active form of hepatocyte growth factor induced met, focal adhesion kinase and protein kinase B activation on neural stem/progenitor cell motility
    Authors: Fang, JD;Lee, SL
    Contributors: Institute of Cellular and Systems Medicine
    Abstract: Hepatocyte growth factor (HGF) is a chemoattractant and inducer for neural stem/progenitor (NS/P) cell migration. Although the type II transmembrane serine protease, matriptase (MTP) is an activator of the latent HGF, MTP is indispensable on NS/P cell motility induced by the active form of HGF. This suggests that MTP's action on NS/P cell motility involves mechanisms other than proteolytic activation of HGF. In the present study, we investigate the role of MTP in HGF-stimulated signaling events. Using specific inhibitors of phosphatidylinositol-3-kinase (PI3K), protein kinase B (Akt) or focal adhesion kinase FAK, we demonstrated that in NS/P cells HGF-activated c-Met induces PI3k-Akt signaling which then leads to FAK activation. This signaling pathway ultimately induces MMP2 expression and NS/P cell motility. Knocking down of MTP in NS/P cells with specific siRNA impaired HGF-stimulation of c-Met, Akt and FAK activation, blocked HGF-induced production of MMP2 and inhibited HGF-stimulated NS/P cell motility. MTP-knockdown NS/P cells cultured in the presence of recombinant protein of MTP protease domain or transfected with the full-length wild-type but not the protease-defected MTP restored HGF-responsive events in NS/P cells. In addition to functioning as HGF activator, our data revealed novel function of MTP on HGF-stimulated c-Met signaling activation.
    Date: 2014-07
    Relation: Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 2014 Jul;1743(7):1285-1294.
    Link to: http://dx.doi.org/10.1016/j.bbamcr.2014.03.020
    JIF/Ranking 2023: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=NHRI&SrcApp=NHRI_IR&KeyISSN=0167-4889&DestApp=IC2JCR
    Cited Times(WOS): https://www.webofscience.com/wos/woscc/full-record/WOS:000336713600005
    Cited Times(Scopus): http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84898669595
    Appears in Collections:[Sheau-Ling Lee] Periodical Articles

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