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Signaling modulations of mir-206-3p in tooth morphogenesis

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dc.contributor.authorNeupane, S.-
dc.contributor.authorAryal, Y.P.-
dc.contributor.authorKim, T.-Y.-
dc.contributor.authorYeon, C.-Y.-
dc.contributor.authorAn, C.-H.-
dc.contributor.authorKim, J.-Y.-
dc.contributor.authorYamamoto, H.-
dc.contributor.authorLee, Y.-
dc.contributor.authorSohn, W.-J.-
dc.contributor.authorKim, J.-Y.-
dc.date.available2020-08-27T05:35:38Z-
dc.date.created2020-08-10-
dc.date.issued2020-08-
dc.identifier.issn1661-6596-
dc.identifier.urihttps://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/78050-
dc.description.abstractMicroRNAs (miRNAs) are a class of naturally occurring small non-coding RNAs that post-transcriptionally regulate gene expression in organisms. Most mammalian miRNAs influence biological processes, including developmental changes, tissue morphogenesis and the maintenance of tissue identity, cell growth, differentiation, apoptosis, and metabolism. The miR-206-3p has been correlated with cancer; however, developmental roles of this miRNA are unclear. In this study, we examined the expression pattern and evaluated the developmental regulation of miR-206-3p during tooth morphogenesis using ex-vivo culture method. The expression pattern of miR-206-3p was examined in the epithelium and mesenchyme of developing tooth germ with stage-specific manners. Perturbation of the expression of miR-206-3p clearly altered expression patterns of dental-development–related signaling molecules, including Axin2, Bmp2, Fgf4, Lef1 and Shh. The gene expression complemented with change in cellular events including, apoptosis and proliferation which caused altered crown and pulp morphogenesis in renal-capsule–calcified teeth. Especially, mislocalization of β-Catenin and SMAD1/5/8 were observed alongside dramatic alterations in the expression patterns of Fgf4 and Shh. Overall, our data suggest that the miR-206-3p regulate the cellular physiology during tooth morphogenesis through modulation of the Wnt, Bmp, Fgf, and Shh signaling pathways to form proper tooth pulp and crown. © 2020 by the authors. Licensee MDPI, Basel, Switzerland.-
dc.language영어-
dc.language.isoen-
dc.publisherMDPI AG-
dc.relation.isPartOfInternational Journal of Molecular Sciences-
dc.titleSignaling modulations of mir-206-3p in tooth morphogenesis-
dc.typeArticle-
dc.type.rimsART-
dc.description.journalClass1-
dc.identifier.wosid000559251100001-
dc.identifier.doi10.3390/ijms21155251-
dc.identifier.bibliographicCitationInternational Journal of Molecular Sciences, v.21, no.15, pp.1 - 15-
dc.description.isOpenAccessN-
dc.identifier.scopusid2-s2.0-85088811666-
dc.citation.endPage15-
dc.citation.startPage1-
dc.citation.titleInternational Journal of Molecular Sciences-
dc.citation.volume21-
dc.citation.number15-
dc.contributor.affiliatedAuthorKim, J.-Y.-
dc.type.docTypeArticle-
dc.subject.keywordAuthorEpigenetic regulation-
dc.subject.keywordAuthorEpithelial-mesenchymal interactions-
dc.subject.keywordAuthorSignaling regulations-
dc.subject.keywordAuthorTooth crown formation-
dc.subject.keywordPlusaxin-
dc.subject.keywordPlusaxin2-
dc.subject.keywordPlusbeta catenin-
dc.subject.keywordPlusbone morphogenetic protein 2-
dc.subject.keywordPlusfibroblast growth factor 4-
dc.subject.keywordPluslymphoid enhancer factor 1-
dc.subject.keywordPlusmicroRNA-
dc.subject.keywordPlusmicroRNA 206 3p-
dc.subject.keywordPluspeptides and proteins-
dc.subject.keywordPlusSmad1 protein-
dc.subject.keywordPlusSmad5 protein-
dc.subject.keywordPlusSmad8 protein-
dc.subject.keywordPlussonic hedgehog protein-
dc.subject.keywordPlusunclassified drug-
dc.subject.keywordPlusadult-
dc.subject.keywordPlusanimal experiment-
dc.subject.keywordPlusanimal model-
dc.subject.keywordPlusanimal tissue-
dc.subject.keywordPlusapoptosis-
dc.subject.keywordPlusArticle-
dc.subject.keywordPluscell function-
dc.subject.keywordPluscell proliferation-
dc.subject.keywordPluscontrolled study-
dc.subject.keywordPlusembryo-
dc.subject.keywordPlusepigenetics-
dc.subject.keywordPlusepithelial mesenchymal transition-
dc.subject.keywordPlushistology-
dc.subject.keywordPlusimmunohistochemistry-
dc.subject.keywordPlusin situ hybridization-
dc.subject.keywordPlusmorphogenesis-
dc.subject.keywordPlusmouse-
dc.subject.keywordPlusnonhuman-
dc.subject.keywordPluspulp morphogenesis-
dc.subject.keywordPlusreal time polymerase chain reaction-
dc.subject.keywordPlusshh signaling-
dc.subject.keywordPlussignal transduction-
dc.subject.keywordPlustooth crown formation-
dc.subject.keywordPlustooth development-
dc.subject.keywordPlusTUNEL assay-
dc.subject.keywordPlusWnt signaling-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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