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        <identifier>oai:fmu.repo.nii.ac.jp:02001900</identifier>
        <datestamp>2024-12-02T02:11:42Z</datestamp>
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          <dc:title>Membrane type 1-matrix metalloproteinase (MT1-MMP) identified as a multifunctional regulator of vascular responses</dc:title>
          <dc:creator>Ohkawara, Hiroshi</dc:creator>
          <dc:creator>Ikeda, Kazuhiko</dc:creator>
          <dc:creator>Ogawa, Kazuei</dc:creator>
          <dc:creator>Takeishi, Yasuchika</dc:creator>
          <dc:subject>MT1-MMP</dc:subject>
          <dc:subject>endothelial dysfunction</dc:subject>
          <dc:subject>atherosclerosis</dc:subject>
          <dc:subject>cardiovascular disease</dc:subject>
          <dc:description>Membrane type 1-matrix metalloproteinase (MT1-MMP) functions as a signaling molecules in addition to a transmembrane metalloprotease, which degrades interstitial collagens and extracellular matrix components. This review focuses on the multifunctional roles of MT1-MMP as a signaling molecule in vascular responses to pro-atherosclerotic stimuli in the pathogenesis of cardiovascular diseases. First, the lectin-like oxidized low-density lipoprotein receptor-1 (LOX-1)-MT1-MMP signaling axis contributes to endothelial dysfunction, which is mediated via small GTP-binding protein RhoA and Rac1 activation. Second, MT1-MMP plays a crucial role in reactive oxygen species (ROS) generation through the activation of receptor for advanced glycation end products (AGEs) in smooth muscle cells, indicating that MT1-MMP may be a therapeutic target for diabetic vascular complications. Third, MT1-MMP is involved in RhoA/Rac1 activation and Ca^{2+} signaling in the mechanism of thrombin-stimulated endothelial dysfunction and oxidant stress. Fourth, the inhibition of the MT1-MMP/Akt signaling pathway may be an attractive strategy for treating endothelial disordered hemostasis in the development of vascular diseases linked to TNF-α-induced inflammation. Fifth, MT1-MMP through RAGE induced RhoA/Rac1 activation and tissue factor protein upregulation through NF-κB phosphorylation in endothelial cells stimulated by high-mobility group box-1, which plays a key role in the systemic inflammation. These findings suggest that the MT1-MMP-mediated signaling axis may be a promising target for treating atherosclerosis and subsequent cardiovascular diseases.</dc:description>
          <dc:description>http://purl.org/coar/resource_type/c_6501</dc:description>
          <dc:publisher>The Fukushima Society of Medical Science</dc:publisher>
          <dc:date>2015</dc:date>
          <dc:type>VoR</dc:type>
          <dc:identifier>0016-2590</dc:identifier>
          <dc:identifier>2185-4610</dc:identifier>
          <dc:identifier>AA0065246X</dc:identifier>
          <dc:identifier>Fukushima Journal of Medical Science</dc:identifier>
          <dc:identifier>2</dc:identifier>
          <dc:identifier>61</dc:identifier>
          <dc:identifier>100</dc:identifier>
          <dc:identifier>91</dc:identifier>
          <dc:identifier>https://fmu.repo.nii.ac.jp/records/2001900</dc:identifier>
          <dc:language>eng</dc:language>
          <dc:relation>https://doi.org/10.5387/fms.2015-15</dc:relation>
          <dc:relation>26370683</dc:relation>
          <dc:relation>2017088012</dc:relation>
          <dc:rights>© 2015 The Fukushima Society of Medical Science</dc:rights>
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