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    <title>Lutgens, E.</title>
    <link>http://repub.eur.nl/res/aut/7846/</link>
    <description>List of Publications</description>
    <language>en</language>
    <image>
      <url>http://repub.eur.nl/static-eur/img/logo.png</url>
      <title>RePub, Erasmus University Rotterdam</title>
      <link>http://repub.eur.nl</link>
    </image>
    <item>
      <title>The APO(*)E3-Leiden mouse as an animal model for basal laminar deposit (Article)</title>
      <link>http://repub.eur.nl/res/pub/9542/</link>
      <pubDate>2000-01-01T00:00:00Z</pubDate>
      <description>AIM: To investigate the APO(*)E3-Leiden mouse as an animal model for age
      related maculopathy (ARM) related extracellular deposits. METHODS: Eyes
      were obtained from APO(*)E3-Leiden transgenic mice on a high
      fat/cholesterol (HFC) diet (n=12) or on a normal mouse chow (n=6), for 9
      months. As controls, eyes were collected from APO-E knockout mice on the
      same diets. From each mouse one eye was processed for microscopic
      evaluation and immunohistochemistry with a polyclonal antibody directed
      against human apo-E. Electron microscopy was also performed. RESULTS: All
      12 eyes of the APO(*)E3-Leiden mice on an HFC diet contained basal laminar
      deposit (BLD; class 1 to class 3), whereas two of six APO(*)E3-Leiden mice
      on normal chow showed BLD class 1. The ultrastructural aspects of this BLD
      were comparable with those seen in early BLD in humans, and BLD showed
      immunoreaction with anti-human-apo-E antibodies. No BLD was found in any
      of the control mice. Drusen were not detected in any of the mice.
      CONCLUSION: These results indicate that APO(*)E3-Leiden mice can be used
      as animal model for the pathogenesis of BLD, and that a HFC diet enhances
      the accumulation of this deposit. Furthermore, this study supports the
      previously suggested involvement of dysfunctional apo-E in the
      accumulation of extracellular deposits in ARM.</description>
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