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首页> 外文期刊>Journal of cellular and molecular medicine. >MicroRNA expression profile of human periodontal ligament cells under the influence of Porphyromonas gingivalis LPS
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MicroRNA expression profile of human periodontal ligament cells under the influence of Porphyromonas gingivalis LPS

机译:牙龈卟啉单胞菌LPS影响下人牙周膜细胞微RNA表达谱

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Periodontitis is a chronic inflammatory disease which is caused by bacterial infection and leads to the destruction of periodontal tissues and resorption of alveolar bone. Thus, special attention should be paid to the mechanism under lipopolysaccharide (LPS)-induced periodontitis because LPS is the major cause of periodontitis. However, to date, miRNA expression in the LPS-induced periodontitis has not been well characterized. In this study, we investigated miRNA expression patterns in LPS-treated periodontal ligament cells (PDLCs). Through miRNA array and differential analysis, 22 up-regulated miRNAs and 28 down-regulated miRNAs in LPS-treated PDLCs were identified. Seven randomly selected up-regulated (miR-21-5p, 498, 548a-5p) and down-regulated (miR-495-3p, 539-5p, 34c-3p and 7a-2-3p) miRNAs were examined by qRT-PCR, and the results proved the accuracy of the miRNA array. Moreover, targets of these deregulated miRNAs were analysed using the miRWalk database. Database for Annotation, Visualization and Integration Discovery software were performed to analyse the Gene Ontology and Kyoto Encyclopaedia of Genes and Genomes pathway of differential expression miRNAs, and the results shown that Toll-like receptor signalling pathway, cAMP signalling pathway, transforming growth factor-beta signalling pathway, mitogen-activated protein kinase (MAPK) signalling pathway and other pathways were involved in the molecular mechanisms underlying LPS-induced periodontitis. In conclusion, this study provides clues for enhancing our understanding of the mechanisms and roles of miRNAs as key regulators of LPS-induced periodontitis.
机译:牙周炎是一种慢性炎性疾病,由细菌感染引起,导致牙周组织破坏和牙槽骨吸收。因此,应特别注意脂多糖(LPS)引起的牙周炎的机制,因为LPS是牙周炎的主要原因。然而,迄今为止,尚未很好地表征LPS诱导的牙周炎中miRNA的表达。在这项研究中,我们调查了LPS处理的牙周膜细胞(PDLC)中的miRNA表达模式。通过miRNA阵列和差异分析,在LPS处理的PDLC中鉴定出22个上调的miRNA和28个下调的miRNA。通过qRT-PCR检测了七个随机选择的上调(miR-21-5p,498、548a-5p)和下调(miR-495-3p,539-5p,34c-3p和7a-2-3p)miRNA。 PCR,结果证明了miRNA阵列的准确性。此外,使用miRWalk数据库分析了这些失控的miRNA的靶标。用Annotation,Visualization和Integration Discovery软件数据库分析差异表达miRNA的基因本体论和《京都议定书》的基因和基因组途径,结果显示Toll样受体信号传导途径,cAMP信号传导途径,转化生长因子-β信号通路,促分裂原活化蛋白激酶(MAPK)信号通路和其他通路参与了LPS诱导的牙周炎的分子机制。总之,这项研究为增强我们对miRNAs作为LPS诱导的牙周炎的关键调节因子的机制和作用的理解提供了线索。

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