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Article: Cannabidiol alleviates LPS-inhibited odonto/osteogenic differentiation in human dental pulp stem cells in vitro

TitleCannabidiol alleviates LPS-inhibited odonto/osteogenic differentiation in human dental pulp stem cells in vitro
Authors
Keywordscannabidiol
dental pulp stem cells
Notch signalling pathway
odonto/osteogenic differentiation
Issue Date1-Mar-2025
PublisherWiley
Citation
International Endodontic Journal, 2025, v. 58, n. 3, p. 449-466 How to Cite?
AbstractAim: Cannabidiol (CBD), derived from the Cannabis sativa plant, exhibits benefits in potentially alleviating a number of oral and dental pathoses, including pulpitis and periodontal diseases. This study aimed to explore the impact of CBD on several traits of human dental pulp stem cells (hDPSC), such as their proliferation, apoptosis, migration and odonto/osteogenic differentiation. Methodology: hDPSCs were harvested from human dental pulp tissues. The cells were treated with CBD at concentrations of 1.25, 2.5, 5, 10, 25 and 50 μg/mL. Cell responses in terms of cell proliferation, colony-forming unit, cell cycle progression, cell migration, apoptosis and odonto/osteogenic differentiation of hDPSCs were assessed in the normal culture condition and P. gingivalis lipopolysaccharide (LPS)-induced ‘inflammatory’ milieus. RNA sequencing and proteomic analysis were performed to predict target pathways impacted by CBD. Results: CBD minimally affects hDPSCs' behaviour under normal culture growth milieu in normal conditions. However, an optimal concentration of 1.25 μg/mL CBD significantly countered the harmful effects of LPS, indicated by the promoting cell proliferation and restoring the odonto/osteogenic differentiation potential of hDPSCs under LPS-treated conditions. The proteomic analysis demonstrated that several proteins involved in cell proliferation and differentiation were upregulated following CBD exposure, including CCL8, CDC42 and KFL5. RNA sequencing data indicated that CBD upregulated the Notch signalling pathway. In an inhibitory experiment, DAPT, a Notch inhibitor, reduced the effect of CBD-rescued LPS-attenuated mineralization in hDPSCs, suggesting that CBD potentially mediates Notch activation to exert its impact on odonto/osteogenic differentiation of hDPSCs. Conclusions: CBD recovers the proliferation and survival of hDPSCs following exposure to LPS. Additionally, we report that CBD-mediated Notch activation effectively restores the odonto/osteogenic differentiation ability of hDPSCs under inflamed conditions. These results underscore the potential role of CBD as a therapeutic option to enhance dentine regeneration.
Persistent Identifierhttp://hdl.handle.net/10722/366341
ISSN
2023 Impact Factor: 5.4
2023 SCImago Journal Rankings: 2.155

 

DC FieldValueLanguage
dc.contributor.authorKornsuthisopon, Chatvadee-
dc.contributor.authorChansaenroj, Ajjima-
dc.contributor.authorSuwittayarak, Ravipha-
dc.contributor.authorPhothichailert, Suphalak-
dc.contributor.authorUsarprom, Khunakon-
dc.contributor.authorSrikacha, Apicha-
dc.contributor.authorVimolmangkang, Sornkanok-
dc.contributor.authorPhrueksotsai, Chaloemrit-
dc.contributor.authorSamaranayake, Lakshman P-
dc.contributor.authorOsathanon, Thanaphum-
dc.date.accessioned2025-11-25T04:18:51Z-
dc.date.available2025-11-25T04:18:51Z-
dc.date.issued2025-03-01-
dc.identifier.citationInternational Endodontic Journal, 2025, v. 58, n. 3, p. 449-466-
dc.identifier.issn0143-2885-
dc.identifier.urihttp://hdl.handle.net/10722/366341-
dc.description.abstractAim: Cannabidiol (CBD), derived from the Cannabis sativa plant, exhibits benefits in potentially alleviating a number of oral and dental pathoses, including pulpitis and periodontal diseases. This study aimed to explore the impact of CBD on several traits of human dental pulp stem cells (hDPSC), such as their proliferation, apoptosis, migration and odonto/osteogenic differentiation. Methodology: hDPSCs were harvested from human dental pulp tissues. The cells were treated with CBD at concentrations of 1.25, 2.5, 5, 10, 25 and 50 μg/mL. Cell responses in terms of cell proliferation, colony-forming unit, cell cycle progression, cell migration, apoptosis and odonto/osteogenic differentiation of hDPSCs were assessed in the normal culture condition and P. gingivalis lipopolysaccharide (LPS)-induced ‘inflammatory’ milieus. RNA sequencing and proteomic analysis were performed to predict target pathways impacted by CBD. Results: CBD minimally affects hDPSCs' behaviour under normal culture growth milieu in normal conditions. However, an optimal concentration of 1.25 μg/mL CBD significantly countered the harmful effects of LPS, indicated by the promoting cell proliferation and restoring the odonto/osteogenic differentiation potential of hDPSCs under LPS-treated conditions. The proteomic analysis demonstrated that several proteins involved in cell proliferation and differentiation were upregulated following CBD exposure, including CCL8, CDC42 and KFL5. RNA sequencing data indicated that CBD upregulated the Notch signalling pathway. In an inhibitory experiment, DAPT, a Notch inhibitor, reduced the effect of CBD-rescued LPS-attenuated mineralization in hDPSCs, suggesting that CBD potentially mediates Notch activation to exert its impact on odonto/osteogenic differentiation of hDPSCs. Conclusions: CBD recovers the proliferation and survival of hDPSCs following exposure to LPS. Additionally, we report that CBD-mediated Notch activation effectively restores the odonto/osteogenic differentiation ability of hDPSCs under inflamed conditions. These results underscore the potential role of CBD as a therapeutic option to enhance dentine regeneration.-
dc.languageeng-
dc.publisherWiley-
dc.relation.ispartofInternational Endodontic Journal-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectcannabidiol-
dc.subjectdental pulp stem cells-
dc.subjectNotch signalling pathway-
dc.subjectodonto/osteogenic differentiation-
dc.titleCannabidiol alleviates LPS-inhibited odonto/osteogenic differentiation in human dental pulp stem cells in vitro-
dc.typeArticle-
dc.identifier.doi10.1111/iej.14183-
dc.identifier.pmid39697062-
dc.identifier.scopuseid_2-s2.0-85212525522-
dc.identifier.volume58-
dc.identifier.issue3-
dc.identifier.spage449-
dc.identifier.epage466-
dc.identifier.eissn1365-2591-
dc.identifier.issnl0143-2885-

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