An Aminopropyl Carbazole Derivative Induces Neurogenesis by Increasing Final Cell Division in Neural Stem Cells
DC Field | Value | Language |
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dc.contributor.author | Shin, Jae-Yeon | - |
dc.contributor.author | Kong, Sun-Young | - |
dc.contributor.author | Yoon, Hye Jin | - |
dc.contributor.author | Ann, Jihyae | - |
dc.contributor.author | Lee, Jeewoo | - |
dc.contributor.author | Kim, Hyun-Jung | - |
dc.date.available | 2019-03-08T16:59:25Z | - |
dc.date.issued | 2015-07 | - |
dc.identifier.issn | 1976-9148 | - |
dc.identifier.issn | 2005-4483 | - |
dc.identifier.uri | https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/9358 | - |
dc.description.abstract | P7C3 and its derivatives, 1-(3,6-dibromo-9H-carbazol-9-yl)-3-(p-tolylamino)propan-2-ol (1) and N-(3-(3,6-dibromo-9H-carbazol-9-yl)-2-hydroxypropy1)-N-(3-methoxyphenyl)-4-methylbenzenesulfonamide (2), were previously reported to increase neurogenesis in rat neural stem cells (NSCs). Although P7C3 is known to increase neurogenesis by protecting newborn neurons, it is not known whether its derivatives also have protective effects to increase neurogenesis. In the current study, we examined how 1 induces neurogenesis. The treatment of 1 in NSCs increased numbers of cells in the absence of epidermal growth factor (EGF) and fibroblast growth factor 2 (FGF2), while not affecting those in the presence of growth factors. Compound 1 did not induce astrocytogenesis during NSC differentiation. 5-Bromo-2'-deoxyuridine (BrdU) pulsing experiments showed that 1 significantly enhanced BrdU-positive neurons. Taken together, our data suggest that 1 promotes neurogenesis by the induction of final cell division during NSC differentiation. | - |
dc.format.extent | 7 | - |
dc.language | 영어 | - |
dc.language.iso | ENG | - |
dc.publisher | KOREAN SOC APPLIED PHARMACOLOGY | - |
dc.title | An Aminopropyl Carbazole Derivative Induces Neurogenesis by Increasing Final Cell Division in Neural Stem Cells | - |
dc.type | Article | - |
dc.identifier.doi | 10.4062/biomolther.2015.016 | - |
dc.identifier.bibliographicCitation | BIOMOLECULES & THERAPEUTICS, v.23, no.4, pp 313 - 319 | - |
dc.identifier.kciid | ART002002098 | - |
dc.description.isOpenAccess | N | - |
dc.identifier.wosid | 000357441700002 | - |
dc.identifier.scopusid | 2-s2.0-84934288627 | - |
dc.citation.endPage | 319 | - |
dc.citation.number | 4 | - |
dc.citation.startPage | 313 | - |
dc.citation.title | BIOMOLECULES & THERAPEUTICS | - |
dc.citation.volume | 23 | - |
dc.type.docType | Article | - |
dc.publisher.location | 대한민국 | - |
dc.subject.keywordAuthor | Neurodegenerative diseases | - |
dc.subject.keywordAuthor | Neural stem cells | - |
dc.subject.keywordAuthor | Neurogenesis | - |
dc.subject.keywordAuthor | Final cell division | - |
dc.subject.keywordAuthor | Aminopropyl carbazoles | - |
dc.subject.keywordPlus | PROGENITOR CELLS | - |
dc.subject.keywordPlus | NEUROPROTECTIVE EFFICACY | - |
dc.subject.keywordPlus | SMALL-MOLECULE | - |
dc.subject.keywordPlus | MOUSE MODEL | - |
dc.subject.keywordPlus | DISEASE | - |
dc.subject.keywordPlus | NEURONS | - |
dc.subject.keywordPlus | GROWTH | - |
dc.subject.keywordPlus | BRAIN | - |
dc.relation.journalResearchArea | Biochemistry & Molecular Biology | - |
dc.relation.journalResearchArea | Pharmacology & Pharmacy | - |
dc.relation.journalWebOfScienceCategory | Biochemistry & Molecular Biology | - |
dc.relation.journalWebOfScienceCategory | Pharmacology & Pharmacy | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.description.journalRegisteredClass | kci | - |
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