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Induction of neural stem cell-like cells (NSCLCs) from mouse astrocytes by Bmi1

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dc.contributor.authorMoon, Jai-Hee-
dc.contributor.authorYoon, Byung Sun-
dc.contributor.authorKim, Bona-
dc.contributor.authorPark, Gyuman-
dc.contributor.authorJung, Hye-Youn-
dc.contributor.authorMaeng, Isaac-
dc.contributor.authorJun, Eun Kyoung-
dc.contributor.authorYoo, Seung Jun-
dc.contributor.authorKim, Aeree-
dc.contributor.authorOh, Sejong-
dc.contributor.authorWhang, Kwang Youn-
dc.contributor.authorKim, Hyunggee-
dc.contributor.authorKim, Dong-Wook-
dc.contributor.authorKim, Ki Dong-
dc.contributor.authorYou, Seungkwon-
dc.date.accessioned2021-09-09T07:19:32Z-
dc.date.available2021-09-09T07:19:32Z-
dc.date.issued2008-06-27-
dc.identifier.issn0006-291X-
dc.identifier.issn1090-2104-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/123354-
dc.description.abstractRecently, Bmi1 was shown to control the proliferation and self-renewal of neural stem cells (NSCs). In this study, we demonstrated the induction of NSC-like cells (NSCLCs) from mouse astrocytes by Bmi1 under NSC culture conditions. These NSCLCs exhibited the morphology and growth properties of NSCs, and expressed NSC marker genes, including nestin, CD133, and Sox2. In vitro differentiation of NSCLCs resulted in differentiated cell populations containing astrocytes, neurons, and oligodendrocytes. Following treatment with histone deacetylase inhibitors (trichostatin A and valproic acid), the potential of NSCLCs for proliferation, dedifferentiation, and self-renewal was significantly inhibited. Our data indicate that multipotent NSCLCs can be generated directly from astrocytes by the addition of Bmi1. (C) 2008 Elsevier Inc. All rights reserved.-
dc.format.extent6-
dc.language영어-
dc.language.isoENG-
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCE-
dc.titleInduction of neural stem cell-like cells (NSCLCs) from mouse astrocytes by Bmi1-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1016/j.bbrc.2008.04.068-
dc.identifier.scopusid2-s2.0-43149107660-
dc.identifier.wosid000256049700018-
dc.identifier.bibliographicCitationBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.371, no.2, pp 267 - 272-
dc.citation.titleBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.citation.volume371-
dc.citation.number2-
dc.citation.startPage267-
dc.citation.endPage272-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiophysics-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiophysics-
dc.subject.keywordPlusHISTONE DEACETYLASE INHIBITORS-
dc.subject.keywordPlusHUMAN FIBROBLASTS-
dc.subject.keywordPlusDIFFERENTIATION-
dc.subject.keywordPlusBRAIN-
dc.subject.keywordPlusIDENTIFICATION-
dc.subject.keywordPlusPROLIFERATION-
dc.subject.keywordPlusFOREBRAIN-
dc.subject.keywordPlusINK4A/ARF-
dc.subject.keywordPlusLINES-
dc.subject.keywordAuthorneural stem cells-
dc.subject.keywordAuthorastrocytes-
dc.subject.keywordAuthordedifferentiation-
dc.subject.keywordAuthorneural stem cell-like cells-
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