Diomede Francesca, Thangavelu Soundara Rajan, Merciaro Ilaria, D'Orazio Monica, Bramanti Placido, Mazzon Emanuela, Trubiani Oriana
University "G. d'Annunzio", Department of Medical, Oral and Biotechnological Sciences.
Eur J Histochem. 2017 Aug 25;61(3):2826. doi: 10.4081/ejh.2017.2826.
Periodontitis is a chronic oral inflammatory disease produced by bacteria. Gingival retraction and bone and connective tissues resorption are the hallmarks of this disease. Chronic periodontitis may contribute to the risk of onset or progression of neuroinflammatory pathological conditions, such as Alzheimer's disease. The main goal of the present study was to investigate if the role of epigenetic modulations is involved in periodontitis using human periodontal ligament stem cells (hPDLSCs) as an in vitro model system. hPDLSCs were treated with lipopolysaccharide of Porphyromonas gingivalis and the expression of proteins associated with DNA methylation and histone acetylation, such as DNMT1 and p300, respectively, and inflammatory transcription factor NF-kB, were examined. Immunofluorescence, Western blot and next generation sequencing results demonstrated that P. gingivalis lipopolysaccharide significantly reduced DNA methylase DNMT1, while it markedly upregulated the level of histone acetyltransferase p300 and NF-kB in hPDLSCs. Our results showed that P. gingivalis lipopolysaccharide markedly regulate the genes involved in epigenetic mechanism, which may result in inflammation induction. We propose that P. gingivalis lipopolysaccharide-treated hPDLSCs could be a potential in vitro model system to study epigenetics modulations associated with periodontitis, which might be helpful to identify novel biomarkers linked to this oral inflammatory disease.
牙周炎是一种由细菌引起的慢性口腔炎症性疾病。牙龈退缩以及骨和结缔组织吸收是这种疾病的标志。慢性牙周炎可能会增加神经炎症性病理状况(如阿尔茨海默病)的发病或进展风险。本研究的主要目的是使用人牙周膜干细胞(hPDLSCs)作为体外模型系统,研究表观遗传调控在牙周炎中是否起作用。用牙龈卟啉单胞菌的脂多糖处理hPDLSCs,并分别检测与DNA甲基化和组蛋白乙酰化相关的蛋白质(如DNMT1和p300)以及炎症转录因子NF-κB的表达。免疫荧光、蛋白质印迹和下一代测序结果表明,牙龈卟啉单胞菌脂多糖显著降低了DNA甲基化酶DNMT1,同时显著上调了hPDLSCs中组蛋白乙酰转移酶p300和NF-κB的水平。我们的结果表明,牙龈卟啉单胞菌脂多糖显著调节参与表观遗传机制的基因,这可能导致炎症诱导。我们提出,经牙龈卟啉单胞菌脂多糖处理的hPDLSCs可能是研究与牙周炎相关的表观遗传调控的潜在体外模型系统,这可能有助于识别与这种口腔炎症性疾病相关的新型生物标志物。
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