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Induction of GDNF and GFR alpha-1 Following AAV1-Rheb(S16H) Administration in the Hippocampus in vivo

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dc.contributor.authorYun, Dongyoung-
dc.contributor.authorJeon, Min-Tae-
dc.contributor.authorKim, Hyung-Jun-
dc.contributor.authorMoon, Gyeong Joon-
dc.contributor.authorLee, Shinrye-
dc.contributor.authorHa, Chang Man-
dc.contributor.authorShin, Minsang-
dc.contributor.authorKim, Sang Ryong-
dc.date.accessioned2023-08-16T09:48:24Z-
dc.date.available2023-08-16T09:48:24Z-
dc.date.created2022-01-13-
dc.date.issued2020-04-
dc.identifier.issn1226-2560-
dc.identifier.urihttp://scholarworks.bwise.kr/kbri/handle/2023.sw.kbri/631-
dc.description.abstractThe activation of neurotrophic signaling pathways following the upregulation of glial cell line-derived neurotrophic factor (GDNF), a member of the transforming growth factor-beta family, has a potential neuroprotective effect in the adult brain. Herein, We report that hippocampal transduction of adeno-associated virus serotype 1 (AAV1) with a constitutively active form of ras homolog enriched in brain [Rheb(S16H)], which can stimulate the production of brain-derived neurotrophic factor (BDNF) in hippocarnpal neurons, induces the increases in expression of GDNF and GDNF family receptor alpha-1 (GFR alpha-1), in neurons and astrocytes in the hippocampus of rat brain in vivo. Moreover, upregulation of GDNF and GFR alpha-1 contributes to neuroprotection against thrombin-induced neurotoxicity in the hippocampus. These results suggest that AAV1-Rheb(S16H) transduction of hippocampal neurons, resulting in neurotrophic interactions between neurons and astrocytes, may be useful for neuroprotection in the adult hippocampus.-
dc.language영어-
dc.language.isoen-
dc.publisherKOREAN SOC BRAIN & NEURAL SCIENCE, KOREAN SOC NEURODEGENERATIVE DISEASE-
dc.titleInduction of GDNF and GFR alpha-1 Following AAV1-Rheb(S16H) Administration in the Hippocampus in vivo-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Hyung-Jun-
dc.contributor.affiliatedAuthorLee, Shinrye-
dc.contributor.affiliatedAuthorHa, Chang Man-
dc.identifier.doi10.5607/en19075-
dc.identifier.scopusid2-s2.0-85086414664-
dc.identifier.wosid000547488400006-
dc.identifier.bibliographicCitationEXPERIMENTAL NEUROBIOLOGY, v.29, no.2, pp.164 - 175-
dc.relation.isPartOfEXPERIMENTAL NEUROBIOLOGY-
dc.citation.titleEXPERIMENTAL NEUROBIOLOGY-
dc.citation.volume29-
dc.citation.number2-
dc.citation.startPage164-
dc.citation.endPage175-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.identifier.kciidART002586560-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaResearch & Experimental Medicine-
dc.relation.journalResearchAreaNeurosciences & Neurology-
dc.relation.journalWebOfScienceCategoryMedicine, Research & Experimental-
dc.relation.journalWebOfScienceCategoryNeurosciences-
dc.subject.keywordPlusNEUROTROPHIC FACTOR-
dc.subject.keywordPlusDOPAMINE NEURONS-
dc.subject.keywordPlusPROTECTS-
dc.subject.keywordPlusBDNF-
dc.subject.keywordPlusTRANSDUCTION-
dc.subject.keywordPlusGENE-
dc.subject.keywordPlusHRHEB(S16H)-
dc.subject.keywordPlusRASAGILINE-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusCOMPLEX-
dc.subject.keywordAuthorRheb(S16H)-
dc.subject.keywordAuthorHippocampus-
dc.subject.keywordAuthorAstrocyte-
dc.subject.keywordAuthorGDNF Neuroprotection-
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