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Choroid Plexus Connexin 43 Expression and Gap Junction Flexibility Are Associated with Clinical Features of Acute EAE
Experimental autoimmune encephalomyelitis (EAE) induced by ventricular injection of antimyelin oligodendrocyte antibodies in DA rats showed severe clinical signs 4 to 5 days after injection. Immunocytochemically, connexin 43 (Cx43) expression increased in the choroid plexus and in the subventricular...
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Published in: | Annals of the New York Academy of Sciences 2009-09, Vol.1173 (1), p.75-82 |
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creator | Jovanova-Nesic, K. Koruga, D. Kojic, D. Kostic, V. Rakic, L. Shoenfeld, Y. |
description | Experimental autoimmune encephalomyelitis (EAE) induced by ventricular injection of antimyelin oligodendrocyte antibodies in DA rats showed severe clinical signs 4 to 5 days after injection. Immunocytochemically, connexin 43 (Cx43) expression increased in the choroid plexus and in the subventricular and subgranular zones of the hippocampus during the development of acute EAE, and decreased after the beginning of the remission phase of the disease. Quantitative computing analysis showed a significantly increased Cx43 expression in the choroid plexus at the peak of the disease. Plaque‐pattern expression of the Cx43 in the choroid plexus (CP) of acute EAE correlated with the increased docking and coupling of the Cx43 hemichannels revealed by atomic force microscopy (AFM). The inner diameter of the gap junction (GJ) channels decreased in the CP of acute EAE, measured by AFM. Cell structure conformational changes showed influences the channels' flexibility in acute EAE. |
doi_str_mv | 10.1111/j.1749-6632.2009.04658.x |
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Immunocytochemically, connexin 43 (Cx43) expression increased in the choroid plexus and in the subventricular and subgranular zones of the hippocampus during the development of acute EAE, and decreased after the beginning of the remission phase of the disease. Quantitative computing analysis showed a significantly increased Cx43 expression in the choroid plexus at the peak of the disease. Plaque‐pattern expression of the Cx43 in the choroid plexus (CP) of acute EAE correlated with the increased docking and coupling of the Cx43 hemichannels revealed by atomic force microscopy (AFM). The inner diameter of the gap junction (GJ) channels decreased in the CP of acute EAE, measured by AFM. Cell structure conformational changes showed influences the channels' flexibility in acute EAE.</description><identifier>ISSN: 0077-8923</identifier><identifier>EISSN: 1749-6632</identifier><identifier>DOI: 10.1111/j.1749-6632.2009.04658.x</identifier><identifier>PMID: 19758135</identifier><language>eng</language><publisher>Malden, USA: Blackwell Publishing Inc</publisher><subject>AFM topography ; Animals ; Antibodies ; Atomic force microscopy ; Brain - metabolism ; Brain - pathology ; Brain Chemistry ; Channels ; choroid plexus ; Choroid Plexus - metabolism ; Choroid Plexus - pathology ; Connexin 43 - biosynthesis ; Coupling ; Cx43 ; Docking ; EAE ; Encephalomyelitis, Autoimmune, Experimental - metabolism ; Encephalomyelitis, Autoimmune, Experimental - pathology ; Encephalomyelitis, Autoimmune, Experimental - physiopathology ; Flexibility ; Gap Junctions - physiology ; Hippocampus ; Immunohistochemistry ; Microscopy, Atomic Force ; Rats</subject><ispartof>Annals of the New York Academy of Sciences, 2009-09, Vol.1173 (1), p.75-82</ispartof><rights>2009 New York Academy of Sciences</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5348-1d15bec7d5cf379553cea63b91db95c45fdd97311fad6daaf79878b423eacf013</citedby><cites>FETCH-LOGICAL-c5348-1d15bec7d5cf379553cea63b91db95c45fdd97311fad6daaf79878b423eacf013</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19758135$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jovanova-Nesic, K.</creatorcontrib><creatorcontrib>Koruga, D.</creatorcontrib><creatorcontrib>Kojic, D.</creatorcontrib><creatorcontrib>Kostic, V.</creatorcontrib><creatorcontrib>Rakic, L.</creatorcontrib><creatorcontrib>Shoenfeld, Y.</creatorcontrib><title>Choroid Plexus Connexin 43 Expression and Gap Junction Flexibility Are Associated with Clinical Features of Acute EAE</title><title>Annals of the New York Academy of Sciences</title><addtitle>Ann N Y Acad Sci</addtitle><description>Experimental autoimmune encephalomyelitis (EAE) induced by ventricular injection of antimyelin oligodendrocyte antibodies in DA rats showed severe clinical signs 4 to 5 days after injection. Immunocytochemically, connexin 43 (Cx43) expression increased in the choroid plexus and in the subventricular and subgranular zones of the hippocampus during the development of acute EAE, and decreased after the beginning of the remission phase of the disease. Quantitative computing analysis showed a significantly increased Cx43 expression in the choroid plexus at the peak of the disease. Plaque‐pattern expression of the Cx43 in the choroid plexus (CP) of acute EAE correlated with the increased docking and coupling of the Cx43 hemichannels revealed by atomic force microscopy (AFM). The inner diameter of the gap junction (GJ) channels decreased in the CP of acute EAE, measured by AFM. Cell structure conformational changes showed influences the channels' flexibility in acute EAE.</description><subject>AFM topography</subject><subject>Animals</subject><subject>Antibodies</subject><subject>Atomic force microscopy</subject><subject>Brain - metabolism</subject><subject>Brain - pathology</subject><subject>Brain Chemistry</subject><subject>Channels</subject><subject>choroid plexus</subject><subject>Choroid Plexus - metabolism</subject><subject>Choroid Plexus - pathology</subject><subject>Connexin 43 - biosynthesis</subject><subject>Coupling</subject><subject>Cx43</subject><subject>Docking</subject><subject>EAE</subject><subject>Encephalomyelitis, Autoimmune, Experimental - metabolism</subject><subject>Encephalomyelitis, Autoimmune, Experimental - pathology</subject><subject>Encephalomyelitis, Autoimmune, Experimental - physiopathology</subject><subject>Flexibility</subject><subject>Gap Junctions - physiology</subject><subject>Hippocampus</subject><subject>Immunohistochemistry</subject><subject>Microscopy, Atomic Force</subject><subject>Rats</subject><issn>0077-8923</issn><issn>1749-6632</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNqNkk9v0zAYhy0EYmXjKyCfEJcE_4lj54IUZW0BTYNpmxAny7EdzSVNOjvR0m-PQ6txo_hiy37ex69e_QCAGKU4ro-bFPOsSPKckpQgVKQoy5lIpxdg8fzwEiwQ4jwRBaFn4E0IG4QwERl_Dc5wwZnAlC3AWD30vncGfm_tNAZY9V1nJ9fBjMLltPM2BNd3UHUGrtUOfh07PcwXq4i72rVu2MPSW1iG0GunBmvgkxseYNW6zmnVwpVVwxg1sG9gqcfBwmW5vACvGtUG-_a4n4P71fKu-pxcfVt_qcqrRDOaiQQbzGqruWG6obxgjGqrcloX2NQF0xlrjCk4xbhRJjdKNbwQXNQZoVbpBmF6Dt4fvDvfP442DHLrgrZtqzrbj0HmPGeUivwkGLthGFF0EiRIUJERHsEP_wSxQChKGSanUS4Qw4yQGRUHVPs-BG8bufNuq_xeYiTnaMiNnBMg5wTIORryTzTkFEvfHX8Z6601fwuPWYjApwPw5Fq7_2-xvP5Z3s7HKEgOAhcGOz0LlP8VB005kz-u1_Iuv0RcXGJ5Q38D3x7V6Q</recordid><startdate>200909</startdate><enddate>200909</enddate><creator>Jovanova-Nesic, K.</creator><creator>Koruga, D.</creator><creator>Kojic, D.</creator><creator>Kostic, V.</creator><creator>Rakic, L.</creator><creator>Shoenfeld, Y.</creator><general>Blackwell Publishing Inc</general><scope>BSCLL</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>7ST</scope><scope>C1K</scope><scope>SOI</scope><scope>7SP</scope><scope>7U5</scope><scope>8FD</scope><scope>L7M</scope><scope>7T5</scope><scope>7TK</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>200909</creationdate><title>Choroid Plexus Connexin 43 Expression and Gap Junction Flexibility Are Associated with Clinical Features of Acute EAE</title><author>Jovanova-Nesic, K. ; 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Immunocytochemically, connexin 43 (Cx43) expression increased in the choroid plexus and in the subventricular and subgranular zones of the hippocampus during the development of acute EAE, and decreased after the beginning of the remission phase of the disease. Quantitative computing analysis showed a significantly increased Cx43 expression in the choroid plexus at the peak of the disease. Plaque‐pattern expression of the Cx43 in the choroid plexus (CP) of acute EAE correlated with the increased docking and coupling of the Cx43 hemichannels revealed by atomic force microscopy (AFM). The inner diameter of the gap junction (GJ) channels decreased in the CP of acute EAE, measured by AFM. Cell structure conformational changes showed influences the channels' flexibility in acute EAE.</abstract><cop>Malden, USA</cop><pub>Blackwell Publishing Inc</pub><pmid>19758135</pmid><doi>10.1111/j.1749-6632.2009.04658.x</doi><tpages>8</tpages></addata></record> |
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subjects | AFM topography Animals Antibodies Atomic force microscopy Brain - metabolism Brain - pathology Brain Chemistry Channels choroid plexus Choroid Plexus - metabolism Choroid Plexus - pathology Connexin 43 - biosynthesis Coupling Cx43 Docking EAE Encephalomyelitis, Autoimmune, Experimental - metabolism Encephalomyelitis, Autoimmune, Experimental - pathology Encephalomyelitis, Autoimmune, Experimental - physiopathology Flexibility Gap Junctions - physiology Hippocampus Immunohistochemistry Microscopy, Atomic Force Rats |
title | Choroid Plexus Connexin 43 Expression and Gap Junction Flexibility Are Associated with Clinical Features of Acute EAE |
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