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Article: MicroRNA expression in JAG1/Notch-activated periodontal ligament stem cells

TitleMicroRNA expression in JAG1/Notch-activated periodontal ligament stem cells
Authors
Issue Date1-Dec-2024
PublisherSpringer Nature [academic journals on nature.com]
Citation
BDJ Open, 2024, v. 10, n. 1 How to Cite?
AbstractObjectives: The study explored the expression profile of miRNAs in Notch-activated periodontal ligament stem cells (PDLSCs) and examined their potential cellular targets. Methods: PDLSCs were cultured and treated with indirect immobilized Jagged1. The miRNA expression profile was examined using NanoString analysis. Bioinformatic analysis was performed together with enrichment, and miRNA expression was evaluated and validated using a quantitative polymerase chain reaction (qPCR). Results: A total of 26 miRNAs were differentially expressed in Jagged1 treated PDLSCs compared with the controls. Pathway analysis revealed that altered miRNAs were significantly associated with the transforming growth factor β (TGF-β) signaling pathway. Target prediction analysis demonstrated that 11,170 genes as predictable targets of these altered miRNAs. Enrichment of predicted target genes revealed that they were related to ErbB, Ras and MAPK signaling pathways and small GTPase transduction. Conclusions: The research concludes that several miRNAs are differentially expressed in jagged-1 treated PDLSCs. In translational terms the differential functionality of these miRNAs offer promise for the development of targeted regenerative materials that are necessary for managing lost tissue replacement in periodontal diseases.
Persistent Identifierhttp://hdl.handle.net/10722/366284
ISSN
2023 Impact Factor: 2.5
2023 SCImago Journal Rankings: 0.518

 

DC FieldValueLanguage
dc.contributor.authorKulthanaamondhita, Promphakkon-
dc.contributor.authorKornsuthisopon, Chatvadee-
dc.contributor.authorChansaenroj, Ajjima-
dc.contributor.authorTrachoo, Vorapat-
dc.contributor.authorManokawinchoke, Jeeranan-
dc.contributor.authorSamaranayake, Lakshman-
dc.contributor.authorSrithanyarat, Supreda Suphanantachat-
dc.contributor.authorOsathanon, Thanaphum-
dc.date.accessioned2025-11-25T04:18:33Z-
dc.date.available2025-11-25T04:18:33Z-
dc.date.issued2024-12-01-
dc.identifier.citationBDJ Open, 2024, v. 10, n. 1-
dc.identifier.issn2056-807X-
dc.identifier.urihttp://hdl.handle.net/10722/366284-
dc.description.abstractObjectives: The study explored the expression profile of miRNAs in Notch-activated periodontal ligament stem cells (PDLSCs) and examined their potential cellular targets. Methods: PDLSCs were cultured and treated with indirect immobilized Jagged1. The miRNA expression profile was examined using NanoString analysis. Bioinformatic analysis was performed together with enrichment, and miRNA expression was evaluated and validated using a quantitative polymerase chain reaction (qPCR). Results: A total of 26 miRNAs were differentially expressed in Jagged1 treated PDLSCs compared with the controls. Pathway analysis revealed that altered miRNAs were significantly associated with the transforming growth factor β (TGF-β) signaling pathway. Target prediction analysis demonstrated that 11,170 genes as predictable targets of these altered miRNAs. Enrichment of predicted target genes revealed that they were related to ErbB, Ras and MAPK signaling pathways and small GTPase transduction. Conclusions: The research concludes that several miRNAs are differentially expressed in jagged-1 treated PDLSCs. In translational terms the differential functionality of these miRNAs offer promise for the development of targeted regenerative materials that are necessary for managing lost tissue replacement in periodontal diseases.-
dc.languageeng-
dc.publisherSpringer Nature [academic journals on nature.com]-
dc.relation.ispartofBDJ Open-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.titleMicroRNA expression in JAG1/Notch-activated periodontal ligament stem cells-
dc.typeArticle-
dc.identifier.doi10.1038/s41405-024-00232-5-
dc.identifier.scopuseid_2-s2.0-85195361989-
dc.identifier.volume10-
dc.identifier.issue1-
dc.identifier.eissn2056-807X-
dc.identifier.issnl2056-807X-

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