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      <dc:title>Functional interplay between endothelial nitric oxide synthase and membrane type 1–matrix metalloproteinase in migrating endothelial cells</dc:title>
      <dc:creator>Genís, Laura</dc:creator>
      <dc:creator>Gonzalo, Pilar</dc:creator>
      <dc:creator>Tutor, Antonio S.</dc:creator>
      <dc:creator>Gálvez, Beatriz G.</dc:creator>
      <dc:creator>Martínez Ruiz, Antonio</dc:creator>
      <dc:creator>Zaragoza, Carlos</dc:creator>
      <dc:creator>Lamas, Santiago</dc:creator>
      <dc:creator>Tryggvason, Karl</dc:creator>
      <dc:creator>Apte, Suneel S.</dc:creator>
      <dc:creator>Arroyo, Alicia G.</dc:creator>
      <dc:description>Nitric oxide (NO) is essential for vascular homeostasis and is also a critical modulator of angiogenesis; however, the molecular mechanisms of NO action during angiogenesis remain elusive. We have investigated the potential relationship between NO and membrane type 1–matrix metalloproteinase (MT1-MMP) during endothelial migration and capillary tube formation. Endothelial NO synthase (eNOS) colocalizes with MT1-MMP at motilityassociated structures in migratory human endothelial cells (ECs); moreover, NO is produced at these structures and is released into the medium during EC migration. We have therefore addressed 2 questions: (1) the putative regulation of MT1-MMP by NO in migratory ECs; and
(2) the requirement for MT1-MMP in NOinduced EC migration and tube formation. NO upregulates MT1-MMP membrane clustering on migratory human ECs, and this is accompanied by increased degradation of type I collagen substrate. MT1-MMP membrane expression and localization are impaired in lung ECs from eNOS-deficient mice, and these cells also show impaired migration and tube formation in vitro. Inhibition of MT1-MMP with a neutralizing antibody impairs NOinduced tube formation by human ECs, and NO-induced endothelial migration and tube formation are impaired in lung ECs from mice deficient in MT1-MMP. MT1-MMP thus appears to be a key molecular effector of NO during the EC migration
and angiogenic processes, and is a potential therapeutic target for NO-associated vascular disorders.</dc:description>
      <dc:date>2024-04-05T11:05:16Z</dc:date>
      <dc:date>2024-04-05T11:05:16Z</dc:date>
      <dc:date>2007-10-15</dc:date>
      <dc:type>journal article</dc:type>
      <dc:identifier>0006-4971</dc:identifier>
      <dc:identifier>1528-0020</dc:identifier>
      <dc:identifier>10.1182/blood-2007-01-068080</dc:identifier>
      <dc:identifier>https://hdl.handle.net/20.500.14352/102744</dc:identifier>
      <dc:identifier>https://ashpublications.org/blood/article/110/8/2916/23981/Functional-interplay-between-endothelial-nitric</dc:identifier>
      <dc:language>eng</dc:language>
      <dc:relation>SAF2005-02228</dc:relation>
      <dc:relation>CAM 08.4/0023/2003</dc:relation>
      <dc:relation>GR/SAL/0309/2004</dc:relation>
      <dc:relation>CP03/00 025</dc:relation>
      <dc:relation>SAF2005- 06025</dc:relation>
      <dc:relation>info:eu-repo/grantAgreement/MEC//SAF2006-02410/ES/MODELOS EXPERIMENTALES DE FISIOPATOLOGIA VASCULAR : DE LA MODIFICACION POSTRADUCCIONAL AL ANIMAL TRANSGENICO/</dc:relation>
      <dc:relation>AR47074</dc:relation>
      <dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
      <dc:rights>open access</dc:rights>
      <dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 International</dc:rights>
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