The role of utrophin and Dp71 for assembly of different dystrophin-associated protein complexes (DPCS) in the choroid plexus and microvasculature of the brain
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 co...
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Veröffentlicht in: | Neuroscience 2004, Vol.129 (2), p.403-413 |
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description | 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. |
doi_str_mv | 10.1016/j.neuroscience.2004.06.079 |
format | Article |
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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.</description><identifier>ISSN: 0306-4522</identifier><identifier>EISSN: 1873-7544</identifier><identifier>DOI: 10.1016/j.neuroscience.2004.06.079</identifier><identifier>PMID: 15501597</identifier><identifier>CODEN: NRSCDN</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Animals ; Astrocytes - drug effects ; Astrocytes - metabolism ; Biological and medical sciences ; blood–brain barrier ; Brain Chemistry - physiology ; Capillaries - drug effects ; Capillaries - metabolism ; Cerebral circulation. Blood-brain barrier. Choroid plexus. Cerebrospinal fluid. Circumventricular organ. Meninges ; Cerebrovascular Circulation - physiology ; Choroid Plexus - metabolism ; confocal laser scanning microscopy ; dystrophin ; Dystrophin - analogs & derivatives ; Dystrophin - genetics ; Dystrophin - physiology ; Dystrophin-Associated Proteins - biosynthesis ; Endothelial Cells - drug effects ; Endothelial Cells - metabolism ; Fluorescent Antibody Technique ; Fundamental and applied biological sciences. Psychology ; glial end-foot ; Immunohistochemistry ; mdx 3Cv mice ; Mice ; Mice, Inbred C57BL ; Mice, Inbred mdx ; Mice, Knockout ; Microscopy, Confocal ; Utrophin - genetics ; Utrophin - physiology ; utrophin-knockout mice ; Vertebrates: nervous system and sense organs</subject><ispartof>Neuroscience, 2004, Vol.129 (2), p.403-413</ispartof><rights>2004 IBRO</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c503t-1f4ffea34edeb480ca20204fe214ffe4da3ca9563435b4a2ceb296b1574679b33</citedby><cites>FETCH-LOGICAL-c503t-1f4ffea34edeb480ca20204fe214ffe4da3ca9563435b4a2ceb296b1574679b33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.neuroscience.2004.06.079$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,4024,27923,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16253553$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15501597$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Haenggi, T.</creatorcontrib><creatorcontrib>Soontornmalai, A.</creatorcontrib><creatorcontrib>Schaub, M.C.</creatorcontrib><creatorcontrib>Fritschy, J.-M.</creatorcontrib><title>The role of utrophin and Dp71 for assembly of different dystrophin-associated protein complexes (DPCS) in the choroid plexus and microvasculature of the brain</title><title>Neuroscience</title><addtitle>Neuroscience</addtitle><description>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.</description><subject>Animals</subject><subject>Astrocytes - drug effects</subject><subject>Astrocytes - metabolism</subject><subject>Biological and medical sciences</subject><subject>blood–brain barrier</subject><subject>Brain Chemistry - physiology</subject><subject>Capillaries - drug effects</subject><subject>Capillaries - metabolism</subject><subject>Cerebral circulation. Blood-brain barrier. Choroid plexus. Cerebrospinal fluid. Circumventricular organ. Meninges</subject><subject>Cerebrovascular Circulation - physiology</subject><subject>Choroid Plexus - metabolism</subject><subject>confocal laser scanning microscopy</subject><subject>dystrophin</subject><subject>Dystrophin - analogs & derivatives</subject><subject>Dystrophin - genetics</subject><subject>Dystrophin - physiology</subject><subject>Dystrophin-Associated Proteins - biosynthesis</subject><subject>Endothelial Cells - drug effects</subject><subject>Endothelial Cells - metabolism</subject><subject>Fluorescent Antibody Technique</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>glial end-foot</subject><subject>Immunohistochemistry</subject><subject>mdx 3Cv mice</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Inbred mdx</subject><subject>Mice, Knockout</subject><subject>Microscopy, Confocal</subject><subject>Utrophin - genetics</subject><subject>Utrophin - physiology</subject><subject>utrophin-knockout mice</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0306-4522</issn><issn>1873-7544</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkc9u1DAQxi1ERZfCKyALCQSHBP93ww3tAkWqBBLlbDnOROtVEgc7qdiX4VlxupHaW_FlJM9v5puZD6HXlJSUUPXhUA4wx5Cch8FByQgRJVEl0dUTtKGXmhdaCvEUbQgnqhCSsXP0PKUDyU8K_gydUykJlZXeoL83e8AxdIBDi-cphnHvB2yHBu9GTXEbIrYpQV93x4VofNtChGHCzTGtdJGB4LydoMFjDBPkBi70Ywd_IOF3ux_bn-9x_puyktuHGHzmcnJOdzq9dzHc2uTmzk5zvBtkQeto_fACnbW2S_ByjRfo15fPN9ur4vr712_bT9eFk4RPBW1FnstyAQ3U4pI4ywgjogVGl4RoLHe2kooLLmthmYOaVaqmUgulq5rzC_T21Dcv8HuGNJneJwddZwcIczJK5yNTxR4FaSUo11Rk8OMJzNulFKE1Y_S9jUdDiVlsNAfz0Eaz2GiIMtnGXPxqVZnrHpr70tW3DLxZgXw427XRDs6ne04xyaVc9tqdOMjHu_UQzSrX-AhuMk3w_zPPP7vExU0</recordid><startdate>2004</startdate><enddate>2004</enddate><creator>Haenggi, T.</creator><creator>Soontornmalai, A.</creator><creator>Schaub, M.C.</creator><creator>Fritschy, J.-M.</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7X8</scope></search><sort><creationdate>2004</creationdate><title>The role of utrophin and Dp71 for assembly of different dystrophin-associated protein complexes (DPCS) in the choroid plexus and microvasculature of the brain</title><author>Haenggi, T. ; Soontornmalai, A. ; Schaub, M.C. ; Fritschy, J.-M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c503t-1f4ffea34edeb480ca20204fe214ffe4da3ca9563435b4a2ceb296b1574679b33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Animals</topic><topic>Astrocytes - drug effects</topic><topic>Astrocytes - metabolism</topic><topic>Biological and medical sciences</topic><topic>blood–brain barrier</topic><topic>Brain Chemistry - physiology</topic><topic>Capillaries - drug effects</topic><topic>Capillaries - metabolism</topic><topic>Cerebral circulation. Blood-brain barrier. Choroid plexus. Cerebrospinal fluid. Circumventricular organ. Meninges</topic><topic>Cerebrovascular Circulation - physiology</topic><topic>Choroid Plexus - metabolism</topic><topic>confocal laser scanning microscopy</topic><topic>dystrophin</topic><topic>Dystrophin - analogs & derivatives</topic><topic>Dystrophin - genetics</topic><topic>Dystrophin - physiology</topic><topic>Dystrophin-Associated Proteins - biosynthesis</topic><topic>Endothelial Cells - drug effects</topic><topic>Endothelial Cells - metabolism</topic><topic>Fluorescent Antibody Technique</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>glial end-foot</topic><topic>Immunohistochemistry</topic><topic>mdx 3Cv mice</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Inbred mdx</topic><topic>Mice, Knockout</topic><topic>Microscopy, Confocal</topic><topic>Utrophin - genetics</topic><topic>Utrophin - physiology</topic><topic>utrophin-knockout mice</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Haenggi, T.</creatorcontrib><creatorcontrib>Soontornmalai, A.</creatorcontrib><creatorcontrib>Schaub, M.C.</creatorcontrib><creatorcontrib>Fritschy, J.-M.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Haenggi, T.</au><au>Soontornmalai, A.</au><au>Schaub, M.C.</au><au>Fritschy, J.-M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The role of utrophin and Dp71 for assembly of different dystrophin-associated protein complexes (DPCS) in the choroid plexus and microvasculature of the brain</atitle><jtitle>Neuroscience</jtitle><addtitle>Neuroscience</addtitle><date>2004</date><risdate>2004</risdate><volume>129</volume><issue>2</issue><spage>403</spage><epage>413</epage><pages>403-413</pages><issn>0306-4522</issn><eissn>1873-7544</eissn><coden>NRSCDN</coden><abstract>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.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>15501597</pmid><doi>10.1016/j.neuroscience.2004.06.079</doi><tpages>11</tpages></addata></record> |
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source | MEDLINE; ScienceDirect Journals (5 years ago - present) |
subjects | Animals Astrocytes - drug effects Astrocytes - metabolism Biological and medical sciences blood–brain barrier Brain Chemistry - physiology Capillaries - drug effects Capillaries - metabolism Cerebral circulation. Blood-brain barrier. Choroid plexus. Cerebrospinal fluid. Circumventricular organ. Meninges Cerebrovascular Circulation - physiology Choroid Plexus - metabolism confocal laser scanning microscopy dystrophin Dystrophin - analogs & derivatives Dystrophin - genetics Dystrophin - physiology Dystrophin-Associated Proteins - biosynthesis Endothelial Cells - drug effects Endothelial Cells - metabolism Fluorescent Antibody Technique Fundamental and applied biological sciences. Psychology glial end-foot Immunohistochemistry mdx 3Cv mice Mice Mice, Inbred C57BL Mice, Inbred mdx Mice, Knockout Microscopy, Confocal Utrophin - genetics Utrophin - physiology utrophin-knockout mice Vertebrates: nervous system and sense organs |
title | The role of utrophin and Dp71 for assembly of different dystrophin-associated protein complexes (DPCS) in the choroid plexus and microvasculature of the brain |
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