The role of utrophin and Dp71 for assembly of different dystrophin-associated protein complexes (DPCs) in the choroid plexus and microvasculature of the brain

被引:65
作者
Haenggi, T [1 ]
Soontornmalai, A [1 ]
Schaub, MC [1 ]
Fritschy, JM [1 ]
机构
[1] Univ Zurich, Inst Pharmacol & Toxicol, CH-8057 Zurich, Switzerland
关键词
blood-brain barrier; confocal laser scanning microscopy; dystrophin; glial end-foot; mdx(3Cx) mice; utrophinknockout micee;
D O I
10.1016/j.neuroscience.2004.06.079
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In the brain, utrophin is present in the choroid plexus epithelium and vascular endothelial cells, whereas the short C-terminal isoform of dystrophin (Dp71) is localized in the glial end-feet surrounding blood vessels. Both proteins serve as anchors for the so-called dystrophin-associated protein complex (DPC), composed of isoforms of syntrophin, dystroglycan and dystrobrevin. Numerous transporter proteins and channels have a polarized distribution in vascular endothelial cells and in glial end-feet, suggesting an association with the DPC. We investigated the composition and localization of the DPC in dependence on the anchoring proteins in mice lacking either utrophin (utrophin(0/0) ) or dystrophin isoforms (mdx(3Cv)). Three distinct complexes were identified: (i) associated with utrophin in the basolateral membrane of the choroid plexus epithelium, (ii) associated with utrophin in vascular endothelial cells, and (iii) associated with Dp71 in the glial end-feet. Upon ablation of utrophin or Dp71, the corresponding DPCs were disrupted and no compensation of the missing protein by its homologue was observed. Association of the water channel aquaporin 4 with the glial DPC likewise was disrupted in mdx(3Cv) mice. These results demonstrate the essential role of utrophin and Dp71 for assembly of the DPC and suggest that these proteins contribute to the proper functioning of the cerebrospinal fluid and blood-brain barriers. (C) 2004 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:403 / 413
页数:11
相关论文
共 45 条
[1]  
Aleman V, 2001, HISTOCHEM CELL BIOL, V115, P243
[2]   The molecular basis of water transport in the brain [J].
Amiry-Moghaddam, M ;
Ottersen, OP .
NATURE REVIEWS NEUROSCIENCE, 2003, 4 (12) :991-1001
[3]   Delayed K+ clearance associated with aquaporin-4 mislocalization:: Phenotypic defects in brains of α-syntrophin-null mice [J].
Amiry-Moghaddam, M ;
Williamson, A ;
Palomba, M ;
Eid, T ;
de Lanerolle, NC ;
Nagelhus, EA ;
Adams, ME ;
Froehner, SC ;
Agre, P ;
Ottersen, OP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (23) :13615-13620
[4]   Dysbindin, a novel coiled-coil-containing protein that interacts with the dystrobrevins in muscle and brain [J].
Benson, MA ;
Newey, SE ;
Martin-Rendon, E ;
Hawkes, R ;
Blake, DJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (26) :24232-24241
[5]   β-dystrobrevin, a member of the dystrophin-related protein family [J].
Blake, DJ ;
Nawrotzki, R ;
Loh, NY ;
Górecki, DC ;
Davies, KE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (01) :241-246
[6]   Different dystrophin-like complexes are expressed in neurons and glia [J].
Blake, DJ ;
Hawkes, R ;
Benson, MA ;
Beesley, PW .
JOURNAL OF CELL BIOLOGY, 1999, 147 (03) :645-657
[7]   G-UTROPHIN, THE AUTOSOMAL HOMOLOG OF DYSTROPHIN DP116, IS EXPRESSED IN SENSORY GANGLIA AND BRAIN [J].
BLAKE, DJ ;
SCHOFIELD, JN ;
ZUELLIG, RA ;
GORECKI, DC ;
PHELPS, SR ;
BARNARD, EA ;
EDWARDS, YH ;
DAVIES, KE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (09) :3697-3701
[8]   NEW MDX MUTATION DISRUPTS EXPRESSION OF MUSCLE AND NONMUSCLE ISOFORMS OF DYSTROPHIN [J].
COX, GA ;
PHELPS, SF ;
CHAPMAN, VM ;
CHAMBERLAIN, JS .
NATURE GENETICS, 1993, 4 (01) :87-93
[9]   Differential distribution of the members of the dystrophin glycoprotein complex in mouse retina:: Effect of the mdx3Cv mutation [J].
Dalloz, C ;
Claudepierre, T ;
Rodius, F ;
Mornet, D ;
Sahel, J ;
Rendon, A .
MOLECULAR AND CELLULAR NEUROSCIENCE, 2001, 17 (05) :908-920
[10]   Postsynaptic abnormalities at the neuromuscular junctions of utrophin-deficient mice [J].
Deconinck, AE ;
Potter, AC ;
Tinsley, JM ;
Wood, SJ ;
Vater, R ;
Young, C ;
Metzinger, L ;
Vincent, A ;
Slater, CR ;
Davies, KE .
JOURNAL OF CELL BIOLOGY, 1997, 136 (04) :883-894