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Voltage-dependent Ca2+ channels promote branching morphogenesis of salivary glands by patterning differential growth

DC Field Value Language
dc.contributor.authorKim, Jin Man-
dc.contributor.authorChoi, Seulki-
dc.contributor.authorLee, Sang Woo-
dc.contributor.authorPark, Kyung Pyo-
dc.creator박경표-
dc.date.accessioned2019-04-25T01:24:16Z-
dc.date.available2020-04-05T01:24:16Z-
dc.date.created2019-07-05-
dc.date.created2019-07-05-
dc.date.issued2018-05-
dc.identifier.citationScientific Reports, Vol.8 No.1, p. 7566-
dc.identifier.issn2045-2322-
dc.identifier.urihttps://hdl.handle.net/10371/149351-
dc.description.abstractBranching morphogenesis is a crucial part of early developmental processes in diverse organs, but the detailed mechanism of this morphogenic event remains to be elucidated. Here we introduce an unknown mechanism leading to branching morphogenesis using mouse embryonic organotypic cultures with time-lapse live imaging. We found spatially expressed L-type voltage-dependent Ca2+ channels (VDCCs) in the peripheral layers of developing epithelial buds and identified the VDCCs as a core signaling mediator for patterning branching architecture. In this process, differential growth in peripheral layers by VDCC-induced ERK activity promoted cleft formation through an epithelial buckling-folding mechanism. Our findings reveal an unexpected role of VDCCs in developmental processes, and address a fundamental question regarding the initial process of branching morphogenesis.-
dc.language영어-
dc.language.isoenen
dc.publisherNature Publishing Group-
dc.titleVoltage-dependent Ca2+ channels promote branching morphogenesis of salivary glands by patterning differential growth-
dc.typeArticle-
dc.identifier.doi10.1038/s41598-018-25957-w-
dc.citation.journaltitleScientific Reports-
dc.identifier.wosid000432108700012-
dc.identifier.scopusid2-s2.0-85047092790-
dc.description.srndOAIID:RECH_ACHV_DSTSH_NO:T201809347-
dc.description.srndRECH_ACHV_FG:RR00200001-
dc.description.srndADJUST_YN:-
dc.description.srndEMP_ID:A001677-
dc.description.srndCITE_RATE:4.122-
dc.description.srndFILENAME:SciRep_F.pdf-
dc.description.srndDEPT_NM:치의과학과-
dc.description.srndEMAIL:kppark@snu.ac.kr-
dc.description.srndSCOPUS_YN:Y-
dc.description.srndFILEURL:https://srnd.snu.ac.kr/eXrepEIR/fws/file/acf47166-962b-4e0e-94ff-efab52ce479f/link-
dc.citation.number1-
dc.citation.startpage7566-
dc.citation.volume8-
dc.description.isOpenAccessY-
dc.contributor.affiliatedAuthorLee, Sang Woo-
dc.contributor.affiliatedAuthorPark, Kyung Pyo-
dc.identifier.srndT201809347-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusEPITHELIUM IN-VITRO-
dc.subject.keywordPlusCELL-MIGRATION-
dc.subject.keywordPlusGENE-EXPRESSION-
dc.subject.keywordPlusCALCIUM-CHANNEL-
dc.subject.keywordPlusMAP KINASE-
dc.subject.keywordPlusDYNAMICS-
dc.subject.keywordPlusMECHANISMS-
dc.subject.keywordPlusPATHWAY-
dc.subject.keywordPlusTUBE-
dc.subject.keywordPlusELONGATION-
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