首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Treatment of Periodontal Ligament Stem Cells with MOR and CBD Promotes Cell Survival and Neuronal Differentiation via the PI3K/Akt/mTOR Pathway
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Treatment of Periodontal Ligament Stem Cells with MOR and CBD Promotes Cell Survival and Neuronal Differentiation via the PI3K/Akt/mTOR Pathway

机译:MOR和CBD处理牙周膜干细胞可通过PI3K / Akt / mTOR途径促进细胞存活和神经元分化

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摘要

Periodontal ligament mesenchymal stem cells (hPDLSCs), as well as all mesenchymal stem cells, show self-renewal, clonogenicity, and multi-tissue differentiation proprieties and can represent a valid support for regenerative medicine. We treated hPDLSCs with a combination of Moringin (MOR) and Cannabidiol (CBD), in order to understand if treatment could improve their survival and their in vitro differentiation capacity. Stem cells survival is fundamental to achieve a successful therapy outcome in the re-implanted tissue of patients. Through NGS transcriptome analysis, we found that combined treatment increased hPDLSCs survival, by inhibition of apoptosis as demonstrated by enhanced expression of anti-apoptotic genes and reduction of pro-apoptotic ones. Moreover, we investigated the possible involvement of PI3K/Akt/mTOR pathway, emphasizing a differential gene expression between treated and untreated cells. Furthermore, hPDLSCs were cultured for 48 h in the presence or absence of CBD and MOR and, after confirming the cellular viability through MTT (3-(4,5-dimethylthiazolyl-2)-2,5-diphenyltetrazoliumbromide) assay, we examined the presence of neuronal markers, through immunofluorescence analysis. We found an increased expression of Nestin and GAP43 (growth associated protein 43) in treated cells. In conclusion, hPDLSCs treated with Moringin and Cannabidiol showed an improved survival capacity and neuronal differentiation potential.
机译:牙周膜间充质干细胞(hPDLSCs)以及所有间充质干细胞均具有自我更新,克隆形成和多组织分化的特性,可以为再生医学提供有效的支持。为了了解治疗是否可以提高其生存率和体外分化能力,我们用辣木素(MOR)和卡那比二醇(CBD)的组合治疗了hPDLSC。干细胞存活是在患者的再植入组织中取得成功治疗结果的基础。通过NGS转录组分析,我们发现联合治疗通过抑制细胞凋亡来提高hPDLSCs的存活率,这可以通过增强抗凋亡基因的表达和减少促凋亡基因来证明。此外,我们调查了PI3K / Akt / mTOR途径的可能参与,强调了已处理和未处理细胞之间的差异基因表达。此外,在存在或不存在CBD和MOR的情况下,将hPDLSCs培养48小时,并通过MTT(3-(4,5-二甲基噻唑基-2)-2,5-二苯基四唑溴化物)确认了细胞活力后,我们检查了通过免疫荧光分析发现神经元标记物的存在。我们发现在处理过的细胞中巢蛋白和GAP43(生长相关蛋白43)的表达增加。总之,用辣木素和卡那比二醇治疗的hPDLSCs表现出提高的生存能力和神经元分化潜能。

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