Cited 21 times in
Retrovirally transduced NCAM140 facilitates neuronal fate choice of hippocampal progenitor cells
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 윤채옥 | - |
dc.date.accessioned | 2017-10-26T06:34:57Z | - |
dc.date.available | 2017-10-26T06:34:57Z | - |
dc.date.issued | 2005 | - |
dc.identifier.issn | 0022-3042 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/151029 | - |
dc.description.abstract | Neural cell adhesion molecule (NCAM) influences proliferation and differentiation of neuronal cells. However, only a little is known about the downstream effects of NCAM signalling, such as alterations in gene transcription, which are associated with cell fate choice. To examine whether NCAM plays a role in cell fate choice during hippocampal neurogenesis, we performed a gain-of-function study, using a retroviral vector which contained full-length NCAM140 cDNA and the marker gene EGFP, and found that NCAM140 promoted neurogenesis by activating proneural transcription activators with concurrent inhibition of gliogenesis. The enhanced transcript levels of proneural transcription factors in NCAM140-transduced cells were down-regulated by treatment of the cells with mitogen-activated protein kinase kinase (MEK) inhibitor PD098059. Overall, these findings suggest that NCAM140 may facilitate hippocampal neurogenesis via regulation of proneurogenic transcription factors in an extracellular signal-regulated kinase (ERK)-dependent manner. | - |
dc.description.statementOfResponsibility | restriction | - |
dc.language | English | - |
dc.publisher | Wiley | - |
dc.relation.isPartOf | JOURNAL OF NEUROCHEMISTRY | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.rights | https://creativecommons.org/licenses/by-nc-nd/2.0/kr/ | - |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/2.0/kr/ | - |
dc.subject.MESH | Animals | - |
dc.subject.MESH | Blotting, Western/methods | - |
dc.subject.MESH | Cell Count/methods | - |
dc.subject.MESH | Cell Differentiation/drug effects | - |
dc.subject.MESH | Cell Differentiation/physiology | - |
dc.subject.MESH | Cells, Cultured | - |
dc.subject.MESH | Drug Interactions | - |
dc.subject.MESH | Embryo, Mammalian | - |
dc.subject.MESH | Enzyme Inhibitors/pharmacology | - |
dc.subject.MESH | Extracellular Signal-Regulated MAP Kinases/metabolism | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Flavonoids/pharmacology | - |
dc.subject.MESH | Gene Expression/drug effects | - |
dc.subject.MESH | Gene Expression/physiology | - |
dc.subject.MESH | Green Fluorescent Proteins/metabolism | - |
dc.subject.MESH | Hippocampus/cytology* | - |
dc.subject.MESH | Hippocampus/embryology | - |
dc.subject.MESH | Immunohistochemistry/methods | - |
dc.subject.MESH | Indoles | - |
dc.subject.MESH | Microtubule-Associated Proteins/metabolism | - |
dc.subject.MESH | Neural Cell Adhesion Molecule L1/metabolism | - |
dc.subject.MESH | Neural Cell Adhesion Molecules/physiology* | - |
dc.subject.MESH | Neurons/metabolism* | - |
dc.subject.MESH | Neurons/virology | - |
dc.subject.MESH | Pregnancy | - |
dc.subject.MESH | Protein Isoforms/metabolism | - |
dc.subject.MESH | Proto-Oncogene Proteins c-bcl-2/metabolism | - |
dc.subject.MESH | RNA, Messenger/metabolism | - |
dc.subject.MESH | Rats | - |
dc.subject.MESH | Retroviridae/genetics* | - |
dc.subject.MESH | Retroviridae/physiology | - |
dc.subject.MESH | Reverse Transcriptase Polymerase Chain Reaction/methods | - |
dc.subject.MESH | Sialic Acids/metabolism | - |
dc.subject.MESH | Stem Cells/drug effects | - |
dc.subject.MESH | Stem Cells/physiology* | - |
dc.subject.MESH | Stem Cells/virology | - |
dc.subject.MESH | Transduction, Genetic/methods* | - |
dc.subject.MESH | Tubulin/metabolism | - |
dc.title | Retrovirally transduced NCAM140 facilitates neuronal fate choice of hippocampal progenitor cells | - |
dc.type | Article | - |
dc.publisher.location | England | - |
dc.contributor.college | Research Institutes (연구소) | - |
dc.contributor.department | Institute for Cancer Research (암연구소) | - |
dc.contributor.googleauthor | Ju Hee Kim | - |
dc.contributor.googleauthor | Jung-Ha Lee | - |
dc.contributor.googleauthor | Jin-Yong Park | - |
dc.contributor.googleauthor | Chang-Hwan Park | - |
dc.contributor.googleauthor | Chae-Ok Yun | - |
dc.contributor.googleauthor | Sang-Hun Lee | - |
dc.contributor.googleauthor | Yong-Sung Lee | - |
dc.contributor.googleauthor | Hyeon Son | - |
dc.identifier.doi | 10.1111/j.1471-4159.2005.03208.x | - |
dc.contributor.localId | A02614 | - |
dc.relation.journalcode | J01620 | - |
dc.identifier.eissn | 1471-4159 | - |
dc.identifier.pmid | 15998292 | - |
dc.identifier.url | http://onlinelibrary.wiley.com/doi/10.1111/j.1471-4159.2005.03208.x/abstract | - |
dc.subject.keyword | extracellular signal‐regulated kinase | - |
dc.subject.keyword | hippocampus | - |
dc.subject.keyword | neural cell adhesion molecule | - |
dc.subject.keyword | neurogenesis | - |
dc.subject.keyword | rat | - |
dc.contributor.alternativeName | Yun, Chae Ok | - |
dc.citation.volume | 94 | - |
dc.citation.number | 2 | - |
dc.citation.startPage | 417 | - |
dc.citation.endPage | 424 | - |
dc.identifier.bibliographicCitation | JOURNAL OF NEUROCHEMISTRY, Vol.94(2) : 417-424, 2005 | - |
dc.date.modified | 2017-05-04 | - |
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