Specific AHNAK expression in brain endothelial cells with barrier properties
doi: 10.1002/jcp.20232
pmid: 15493012
Specific AHNAK expression in brain endothelial cells with barrier properties
AbstractThe blood–brain barrier (BBB) is essential for maintaining brain homeostasis and low permeability. Because disruption of the BBB may contribute to many brain disorders, they are of considerable interests in the identification of the molecular mechanisms of BBB development and integrity. We here report that the giant protein AHNAK is expressed at the plasma membrane of endothelial cells (ECs) forming specific blood–tissue barriers, but is absent from the endothelium of capillaries characterized by extensive molecular exchanges between blood and extracellular fluid. In the brain, AHNAK is widely distributed in ECs with BBB properties, where it co‐localizes with the tight junction protein ZO‐1. AHNAK is absent from the permeable brain ECs of the choroid plexus and is down‐regulated in permeable angiogenic ECs of brain tumors. In the choroid plexus, AHNAK accumulates at the tight junctions of the choroid epithelial cells that form the blood–cerebrospinal fluid (CSF) barrier. In EC cultures, the regulation of AHNAK expression and its localization corresponds to general criteria of a protein involved in barrier organization. AHNAK is up‐regulated by angiopoietin‐1 (Ang‐1), a morphogenic factor that regulates brain EC permeability. In bovine cerebral ECs co‐cultured with glial cells, AHNAK relocates from the cytosol to the plasma membrane when endothelial cells acquire BBB properties. Our results identify AHNAK as a protein marker of endothelial cells with barrier properties. © 2004 Wiley‐Liss, Inc.
MESH: Neoplasm Proteins, Male, Wistar, Cell Communication, MESH: Tight Junctions, MESH: Blood-Brain Barrier, Mice, Cytosol, MESH: Cytosol, MESH: Up-Regulation, MESH: Animals, MESH: Endothelial Cells, Brain Neoplasms, Brain, Cell Differentiation, Neoplasm Proteins, MESH: Cattle, Blood-Brain Barrier, MESH: Brain Neoplasms, MESH: Neuroglia, MESH: Membrane Proteins, Neuroglia, MESH: Cell Differentiation, MESH: Protein Transport, MESH: Rats, 610, [SDV.BC]Life Sciences [q-bio]/Cellular Biology, MESH: Phosphoproteins, Cell Line, MESH: Coculture Techniques, MESH: Brain, MESH: Angiopoietin-1, MESH: Cell Communication, 616, Angiopoietin-1, Animals, MESH: Mice, [SDV.BC] Life Sciences [q-bio]/Cellular Biology, Cell Membrane, Endothelial Cells, Membrane Proteins, Newborn, MESH: Male, Coculture Techniques, MESH: Cell Line, Animals, Newborn, MESH: Choroid Plexus, Choroid Plexus, Cattle, MESH: Cell Membrane
MESH: Neoplasm Proteins, Male, Wistar, Cell Communication, MESH: Tight Junctions, MESH: Blood-Brain Barrier, Mice, Cytosol, MESH: Cytosol, MESH: Up-Regulation, MESH: Animals, MESH: Endothelial Cells, Brain Neoplasms, Brain, Cell Differentiation, Neoplasm Proteins, MESH: Cattle, Blood-Brain Barrier, MESH: Brain Neoplasms, MESH: Neuroglia, MESH: Membrane Proteins, Neuroglia, MESH: Cell Differentiation, MESH: Protein Transport, MESH: Rats, 610, [SDV.BC]Life Sciences [q-bio]/Cellular Biology, MESH: Phosphoproteins, Cell Line, MESH: Coculture Techniques, MESH: Brain, MESH: Angiopoietin-1, MESH: Cell Communication, 616, Angiopoietin-1, Animals, MESH: Mice, [SDV.BC] Life Sciences [q-bio]/Cellular Biology, Cell Membrane, Endothelial Cells, Membrane Proteins, Newborn, MESH: Male, Coculture Techniques, MESH: Cell Line, Animals, Newborn, MESH: Choroid Plexus, Choroid Plexus, Cattle, MESH: Cell Membrane
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