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Antioxidative role of selenoprotein W in oxidant-induced mouse embryonic neuronal cell death

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dc.contributor.authorChung, Youn Wook-
dc.contributor.authorJeong, Daewon-
dc.contributor.authorNoh, Ok Jeong-
dc.contributor.authorPark, Yong Hwan-
dc.contributor.authorKang, Soo Im-
dc.contributor.authorLee, Min Goo-
dc.contributor.authorLee, Tae-Hoon-
dc.contributor.authorYim, Moon Bin-
dc.contributor.authorKim, Ick Young-
dc.date.accessioned2021-09-08T17:40:30Z-
dc.date.available2021-09-08T17:40:30Z-
dc.date.created2021-06-10-
dc.date.issued2009-05-
dc.identifier.issn1016-8478-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/120161-
dc.description.abstractIt has been reported that selenoprotein W (SelW) mRNA is highly expressed in the developing central nerve system of rats, and its expression is maintained until the early postnatal stage. We here found that SelW protein significantly increased in mouse brains of postnatal day 8 and 20 relative to embryonic day 15. This was accompanied by increased expression of SOD1 and SOD2. When the expression of SelW in primary cultured cells derived from embryonic cerebral cortex was knocked down with small interfering RNAs (siRNAs), SelW siRNA-transfected neuronal cells were more sensitive to the oxidative stress induced by treatment of H2O2 than control cells. TUNEL assays revealed that H2O2-induced apoptotic cell death occurred at a higher frequency in the siRNA-transfected cells than in the control cells. Taken together, our findings suggest that SelW plays an important role in protection of neurons from oxidative stress during neuronal development.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherKOREAN SOC MOLECULAR & CELLULAR BIOLOGY-
dc.subjectGLUTATHIONE-PEROXIDASE-
dc.subjectTHIOREDOXIN REDUCTASE-
dc.subjectSELENOCYSTEINE INSERTION-
dc.subjectMAMMALIAN SELENOPROTEIN-
dc.subjectMUSCULAR-DYSTROPHY-
dc.subjectEXPRESSION PATTERN-
dc.subjectELONGATION-FACTOR-
dc.subjectDIETARY SELENIUM-
dc.subjectRAT MUSCLE-
dc.subjectBRAIN-
dc.titleAntioxidative role of selenoprotein W in oxidant-induced mouse embryonic neuronal cell death-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Ick Young-
dc.identifier.doi10.1007/s10059-009-0074-3-
dc.identifier.scopusid2-s2.0-66649090050-
dc.identifier.wosid000266349000015-
dc.identifier.bibliographicCitationMOLECULES AND CELLS, v.27, no.5, pp.609 - 613-
dc.relation.isPartOfMOLECULES AND CELLS-
dc.citation.titleMOLECULES AND CELLS-
dc.citation.volume27-
dc.citation.number5-
dc.citation.startPage609-
dc.citation.endPage613-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.identifier.kciidART001343630-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaCell Biology-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryCell Biology-
dc.subject.keywordPlusGLUTATHIONE-PEROXIDASE-
dc.subject.keywordPlusTHIOREDOXIN REDUCTASE-
dc.subject.keywordPlusSELENOCYSTEINE INSERTION-
dc.subject.keywordPlusMAMMALIAN SELENOPROTEIN-
dc.subject.keywordPlusMUSCULAR-DYSTROPHY-
dc.subject.keywordPlusEXPRESSION PATTERN-
dc.subject.keywordPlusELONGATION-FACTOR-
dc.subject.keywordPlusDIETARY SELENIUM-
dc.subject.keywordPlusRAT MUSCLE-
dc.subject.keywordPlusBRAIN-
dc.subject.keywordAuthorantioxidant-
dc.subject.keywordAuthorneuronal cells-
dc.subject.keywordAuthoroxidative stress-
dc.subject.keywordAuthorselenium-
dc.subject.keywordAuthorselenoprotein W-
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