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Astrocyte functions in the copper homeostasis of the brain
Authors:Ivo F Scheiber  Ralf Dringen
Institution:Center for Biomolecular Interactions Bremen, University of Bremen, P.O. Box 330440, D-28334 Bremen, Germany; Center for Environmental Research and Sustainable Technology, Leobener Strasse, D-28359 Bremen, Germany
Abstract:Copper is an essential element that is required for a variety of important cellular functions. Since not only copper deficiency but also excess of copper can seriously affect cellular functions, the cellular copper metabolism is tightly regulated. In brain, astrocytes appear to play a pivotal role in the copper metabolism. With their strategically important localization between capillary endothelial cells and neuronal structures they are ideally positioned to transport copper from the blood–brain barrier to parenchymal brain cells. Accordingly, astrocytes have the capacity to efficiently take up, store and to export copper. Cultured astrocytes appear to be remarkably resistant against copper-induced toxicity. However, copper exposure can lead to profound alterations in the metabolism of these cells. This article will summarize the current knowledge on the copper metabolism of astrocytes, will describe copper-induced alterations in the glucose and glutathione metabolism of astrocytes and will address the potential role of astrocytes in the copper metabolism of the brain in diseases that have been connected with disturbances in brain copper homeostasis.
Keywords:BBB  blood&ndash  brain barrier  CCS  copper chaperone for copper/zinc superoxide dismutase  Ctr1  copper transporter receptor 1  DMT1  divalent metal transporter 1  GSH  glutathione  Hspa5  heat shock 70   kDa protein 5  MTs  metallothioneins  Prp  prion protein  ROS  reactive oxygen species  ZIP  Zrt/IRT-like protein
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