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Keywords {🔍}

article, selenoprotein, endothelial, cells, privacy, cookies, content, information, publish, search, cell, access, data, log, journal, research, histochemistry, rat, tissues, burk, hill, boeglin, liver, oxidant, discover, springer, function, optional, personal, parties, policy, find, track, biology, associates, cite, kristina, martha, ford, ebner, harold, chittum, explore, heparinbinding, injury, kidney, brain, confocal, microscopy, central,

Topics {✒️}

extracellular heparin-binding protein vascular endothelial cells confocal microscopy chlorpyrifos-induced oxidative damage apolipoprotein e-mediated regulation month download article/chapter cell biology aims oxidant injury heparin-binding properties oxidant defense function privacy choices/manage cookies capillary endothelial cells central regions full article pdf 343-6229 e-mail raymond european economic area scope submit manuscript antioxidant enzyme levels selenium distribution conditions privacy policy check access instant access accepting optional cookies related subjects main content log endothelial cells journal finder publish rat tissues article histochemistry privacy policy personal data binding books a optional cookies article log information manage preferences data protection essential cookies cookies skip subscription content similar content article cite article burk institution subscribe journal publish usage analysis social media varying standards july 1997 volume 108

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         headline:Selenoprotein P associates with endothelial cells in rat tissues
         description: Selenoprotein P is an extracellular heparin-binding protein that has been implicated in protecting the liver against oxidant injury. Its location in liver, kidney, and brain was determined by conventional immunohistochemistry and confocal microscopy using a polyclonal antiserum. Selenoprotein P is associated with endothelial cells in the liver and is more abundant in central regions than in portal regions. It is also present in kidney glomeruli associated with capillary endothelial cells. Staining of selenoprotein P in the brain is also confined to vascular endothelial cells. The heparin-binding properties of selenoprotein P could be the basis for its binding to tissue. Its localization to the vicinity of endothelial cells is potentially relevant to its oxidant defense function.
         datePublished:
         dateModified:
         pageStart:11
         pageEnd:15
         sameAs:https://doi.org/10.1007/s004180050141
         keywords:
            Endothelial Cell
            Central Region
            Confocal Microscopy
            Vascular Endothelial Cell
            Oxidant Injury
            Biomedicine
            general
            Cell Biology
            Biochemistry
            Developmental Biology
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      headline:Selenoprotein P associates with endothelial cells in rat tissues
      description: Selenoprotein P is an extracellular heparin-binding protein that has been implicated in protecting the liver against oxidant injury. Its location in liver, kidney, and brain was determined by conventional immunohistochemistry and confocal microscopy using a polyclonal antiserum. Selenoprotein P is associated with endothelial cells in the liver and is more abundant in central regions than in portal regions. It is also present in kidney glomeruli associated with capillary endothelial cells. Staining of selenoprotein P in the brain is also confined to vascular endothelial cells. The heparin-binding properties of selenoprotein P could be the basis for its binding to tissue. Its localization to the vicinity of endothelial cells is potentially relevant to its oxidant defense function.
      datePublished:
      dateModified:
      pageStart:11
      pageEnd:15
      sameAs:https://doi.org/10.1007/s004180050141
      keywords:
         Endothelial Cell
         Central Region
         Confocal Microscopy
         Vascular Endothelial Cell
         Oxidant Injury
         Biomedicine
         general
         Cell Biology
         Biochemistry
         Developmental Biology
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                     name:Division of Gastroenterology, Department of Medicine and Institute for Developmental Neuroscience, The Kennedy Center,Vanderbilt University, Nashville, TN 37232-2279, USA Tel. +1 (615) 343-4747; Fax +1 (615) 343-6229 e-mail [email protected], , US
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            name:Kristina E. Hill
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                     name:Division of Gastroenterology, Department of Medicine and Institute for Developmental Neuroscience, The Kennedy Center,Vanderbilt University, Nashville, TN 37232-2279, USA Tel. +1 (615) 343-4747; Fax +1 (615) 343-6229 e-mail [email protected], , US
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               name:Division of Gastroenterology, Department of Medicine and Institute for Developmental Neuroscience, The Kennedy Center,Vanderbilt University, Nashville, TN 37232-2279, USA Tel. +1 (615) 343-4747; Fax +1 (615) 343-6229 e-mail [email protected], , US
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            address:
               name:Division of Gastroenterology, Department of Medicine and Institute for Developmental Neuroscience, The Kennedy Center,Vanderbilt University, Nashville, TN 37232-2279, USA Tel. +1 (615) 343-4747; Fax +1 (615) 343-6229 e-mail [email protected], , US
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            address:
               name:Division of Gastroenterology, Department of Medicine and Institute for Developmental Neuroscience, The Kennedy Center,Vanderbilt University, Nashville, TN 37232-2279, USA Tel. +1 (615) 343-4747; Fax +1 (615) 343-6229 e-mail [email protected], , US
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            address:
               name:Division of Gastroenterology, Department of Medicine and Institute for Developmental Neuroscience, The Kennedy Center,Vanderbilt University, Nashville, TN 37232-2279, USA Tel. +1 (615) 343-4747; Fax +1 (615) 343-6229 e-mail [email protected], , US
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