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Human neural stem cells over-expressing choline acetyltransferase restore cognition in rat model of cognitive dysfunction

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dc.contributor.authorPark, Dongsun-
dc.contributor.authorLee, Hong Jun-
dc.contributor.authorJoo, Seong Soo-
dc.contributor.authorBae, Dae-Kwon-
dc.contributor.authorYang, Goeun-
dc.contributor.authorYang, Yun-Hui-
dc.contributor.authorLim, Inja-
dc.contributor.authorMatsuo, Akinori-
dc.contributor.authorTooyama, Ikuo-
dc.contributor.authorKim, Yun-Bae-
dc.contributor.authorKim, Seung U.-
dc.date.available2019-05-29T07:37:19Z-
dc.date.issued2012-04-
dc.identifier.issn0014-4886-
dc.identifier.issn1090-2430-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/20399-
dc.description.abstractA human neural stem cell (NSC) line over-expressing human choline acetyltransferase (ChAT) gene was generated and these F3.ChAT NSCs were transplanted into the brain of rat Alzheimer disease (AD) model which was induced by application of ethylcholine mustard aziridinium ion (AF64A) that specifically denatures cholinergic nerves and thereby leads to memory deficit as a salient feature of AD. Transplantation of F3.ChAT human NSCs fully recovered the learning and memory function of AF64A animals, and induced elevated levels of acetylcholine (ACh) in cerebrospinal fluid (CSF). Transplanted F3.ChAT human NSCs were found to migrate to various brain regions including cerebral cortex, hippocampus, striatum and septum, and differentiated into neurons and astrocytes. The present study demonstrates that brain transplantation of human NSCs over-expressing ChAT ameliorates complex learning and memory deficits in AF64A-cholinotoxin-induced AD rat model. (C) 2012 Elsevier Inc. All rights reserved.-
dc.format.extent6-
dc.language영어-
dc.language.isoENG-
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCE-
dc.titleHuman neural stem cells over-expressing choline acetyltransferase restore cognition in rat model of cognitive dysfunction-
dc.typeArticle-
dc.identifier.doi10.1016/j.expneurol.2011.12.040-
dc.identifier.bibliographicCitationEXPERIMENTAL NEUROLOGY, v.234, no.2, pp 521 - 526-
dc.description.isOpenAccessN-
dc.identifier.wosid000301994900030-
dc.identifier.scopusid2-s2.0-84862781166-
dc.citation.endPage526-
dc.citation.number2-
dc.citation.startPage521-
dc.citation.titleEXPERIMENTAL NEUROLOGY-
dc.citation.volume234-
dc.type.docTypeArticle-
dc.publisher.location미국-
dc.subject.keywordAuthorAlzheimer disease-
dc.subject.keywordAuthorAF64A cholinotoxin-
dc.subject.keywordAuthorBrain transplantation-
dc.subject.keywordAuthorCholine acetyltransferase (ChAT)-
dc.subject.keywordAuthorCognitive function-
dc.subject.keywordAuthorNeural stem cell-
dc.subject.keywordPlusMOUSE STROKE MODEL-
dc.subject.keywordPlusALZHEIMERS-DISEASE-
dc.subject.keywordPlusNEUROTROPHIC FACTOR-
dc.subject.keywordPlusFUNCTIONAL RECOVERY-
dc.subject.keywordPlusPROVIDE NEUROPROTECTION-
dc.subject.keywordPlusNEUROLOGICAL DISORDERS-
dc.subject.keywordPlusIN-VIVO-
dc.subject.keywordPlusBRAIN-
dc.subject.keywordPlusTRANSPLANTATION-
dc.subject.keywordPlusIMPROVEMENT-
dc.relation.journalResearchAreaNeurosciences & Neurology-
dc.relation.journalWebOfScienceCategoryNeurosciences-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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