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Catalpol promotes the generation of cerebral organoids with oRGs through activation of STAT3 signaling

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dc.contributor.authorLee, Yoo-Jung-
dc.contributor.authorCho, Byounggook-
dc.contributor.authorKwon, Daeyeol-
dc.contributor.authorKim, Yunkyung-
dc.contributor.authorAn, Saemin-
dc.contributor.authorKang, Soi-
dc.contributor.authorKim, Jongpil-
dc.date.accessioned2025-01-13T06:30:14Z-
dc.date.available2025-01-13T06:30:14Z-
dc.date.issued2025-05-
dc.identifier.issn2380-6761-
dc.identifier.issn2380-6761-
dc.identifier.urihttps://scholarworks.dongguk.edu/handle/sw.dongguk/56663-
dc.description.abstractThe generation of human cortical organoids containing outer radial glia (oRG) cells is crucial for modeling neocortical development. Here we show that Catalpol, an iridoid glucoside derived from Rehmannia glutinosa, significantly enhances the generation of cerebral organoids with expanded oRG populations and increased neurogenic potential. Catalpol-treated organoids exhibited thicker ventricular zone/subventricular zone (VZ/SVZ) and outer subventricular zone (oSVZ) regions, with increased numbers of SOX2 + HOPX+ and SOX2 + TNC+ oRG cells and elevated expression of oRG markers HOPX and FAM107A. We found that Catalpol promoted oRG generation through non-vertical divisions of ventricular radial glia (vRG) cells, indicating enhanced oRG generation via asymmetrical divisions. Furthermore, we demonstrated that Catalpol augmented oRG cell numbers through activation of the STAT3 signaling pathway. These findings highlight Catalpol's potential in promoting the generation of cerebral organoids with expanded oRG populations and increased neurogenic potential through STAT3 activation, offering new insights into neocortical development modeling. © 2024 The Author(s). Bioengineering & Translational Medicine published by Wiley Periodicals LLC on behalf of American Institute of Chemical Engineers.-
dc.format.extent11-
dc.language영어-
dc.language.isoENG-
dc.publisherJohn Wiley and Sons Inc-
dc.titleCatalpol promotes the generation of cerebral organoids with oRGs through activation of STAT3 signaling-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1002/btm2.10746-
dc.identifier.scopusid2-s2.0-85213679568-
dc.identifier.wosid001391772800001-
dc.identifier.bibliographicCitationBioengineering and Translational Medicine, v.10, no.3, pp 1 - 11-
dc.citation.titleBioengineering and Translational Medicine-
dc.citation.volume10-
dc.citation.number3-
dc.citation.startPage1-
dc.citation.endPage11-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalResearchAreaEngineering-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryEngineering, Biomedical-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.subject.keywordPlusOUTER SUBVENTRICULAR ZONE-
dc.subject.keywordPlusJAK2/STAT3 PATHWAY-
dc.subject.keywordPlusRADIAL GLIA-
dc.subject.keywordPlusMODEL-
dc.subject.keywordPlusPROGENITORS-
dc.subject.keywordPlusNEOCORTEX-
dc.subject.keywordPlusIDENTITY-
dc.subject.keywordAuthorCatalpol-
dc.subject.keywordAuthorcerebral organoids-
dc.subject.keywordAuthorouter radial glia cells-
dc.subject.keywordAuthorSTAT3 signaling-
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