ARF6 and EFA6A regulate the development and maintenance of dendritic spines

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dc.contributor.authorChoi, Sko
dc.contributor.authorKo, Jko
dc.contributor.authorLee, JRko
dc.contributor.authorLee, HWko
dc.contributor.authorKim, Kko
dc.contributor.authorChung, HSko
dc.contributor.authorKim, Hko
dc.contributor.authorKim, Eunjoonko
dc.date.accessioned2007-09-19T02:53:53Z-
dc.date.available2007-09-19T02:53:53Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2006-05-
dc.identifier.citationJOURNAL OF NEUROSCIENCE, v.26, no.18, pp.4811 - 4819-
dc.identifier.issn0270-6474-
dc.identifier.urihttp://hdl.handle.net/10203/1483-
dc.description.abstractThe cellular and molecular mechanisms underlying the development and maintenance of dendritic spines are not fully understood. ADP-ribosylation factor 6 ( ARF6) is a small GTPase known to regulate actin remodeling and membrane traffic. Here, we report involvement of ARF6 and exchange factor for ARF6 ( EFA6A) in the regulation of spine development and maintenance. An active form of ARF6 promotes the formation of dendritic spines at the expense of filopodia. EFA6A promotes spine formation in an ARF6 activation-dependent manner. Knockdown of ARF6 and EFA6A by small interfering RNA decreases spine formation. Live imaging indicates that ARF6 knockdown decreases the conversion of filopodia to spines and the stability of early spines. The spine-promoting effect of ARF6 is partially blocked by Rac1. ARF6 and EFA6A protect mature spines from inactivity-induced destabilization. These results suggest that ARF6 and EFA6A may regulate the conversion of filopodia to spines and the stability of both early and mature spines.-
dc.description.sponsorshipThis work was supported by the National Creative Research Initiative Program of the Korean Ministry of Science and Technology (E.K.) and Korea Health 21 Research and Development Project, Ministry of Health and Welfare, Republic of Korea Grant 02-PJ1-PG1-CH06-0001 (H.K.). S.C. is supported in part by the Bojeong Kim fellowship. We thank Dr. Julie G. Donaldson (National Institutes of Health) for pXS-ARF6-HA cDNAs (wild type and T27N) and the Kazusa DNA Research Institute for KIAA2011 cDNA.en
dc.languageEnglish-
dc.language.isoen_USen
dc.publisherSOC NEUROSCIENCE-
dc.subjectHIPPOCAMPAL PYRAMIDAL NEURONS-
dc.subjectNUCLEOTIDE-EXCHANGE PROTEIN-
dc.subjectADP-RIBOSYLATION FACTOR-6-
dc.subjectMORPHOLOGICAL PLASTICITY-
dc.subjectSYNAPTIC PLASTICITY-
dc.subjectACTIN CYTOSKELETON-
dc.subjectSMALL GTPASES-
dc.subjectMEMBRANE-
dc.subjectRHO-
dc.subjectRAC-
dc.titleARF6 and EFA6A regulate the development and maintenance of dendritic spines-
dc.typeArticle-
dc.identifier.wosid000237271700011-
dc.identifier.scopusid2-s2.0-33646934083-
dc.type.rimsART-
dc.citation.volume26-
dc.citation.issue18-
dc.citation.beginningpage4811-
dc.citation.endingpage4819-
dc.citation.publicationnameJOURNAL OF NEUROSCIENCE-
dc.identifier.doi10.1523/JNEUROSCI.4182-05.2006-
dc.contributor.localauthorKim, Eunjoon-
dc.contributor.nonIdAuthorChoi, S-
dc.contributor.nonIdAuthorKo, J-
dc.contributor.nonIdAuthorLee, JR-
dc.contributor.nonIdAuthorLee, HW-
dc.contributor.nonIdAuthorKim, K-
dc.contributor.nonIdAuthorChung, HS-
dc.contributor.nonIdAuthorKim, H-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorspine-
dc.subject.keywordAuthorfilopodia-
dc.subject.keywordAuthorARF6-
dc.subject.keywordAuthorEFA6A-
dc.subject.keywordAuthorRac1-
dc.subject.keywordAuthorsynapse-
dc.subject.keywordPlusHIPPOCAMPAL PYRAMIDAL NEURONS-
dc.subject.keywordPlusNUCLEOTIDE-EXCHANGE PROTEIN-
dc.subject.keywordPlusADP-RIBOSYLATION FACTOR-6-
dc.subject.keywordPlusMORPHOLOGICAL PLASTICITY-
dc.subject.keywordPlusSYNAPTIC PLASTICITY-
dc.subject.keywordPlusACTIN CYTOSKELETON-
dc.subject.keywordPlusSMALL GTPASES-
dc.subject.keywordPlusMEMBRANE-
dc.subject.keywordPlusRHO-
dc.subject.keywordPlusRAC-
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