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机构地区:[1]天津市口腔医院,300041
出 处:《现代口腔医学杂志》2014年第2期107-110,共4页Journal of Modern Stomatology
基 金:天津市卫生局科技基金(09KY20)
摘 要:目的研究高浓度牙龈卟啉单胞菌(Porphyromonas gingivalis,P.g.)脂多糖(lipopolysaccharide,LPS)对人牙周膜成纤维细胞(human periodontal ligament fibroblasts,hPDLFs)中骨唾液酸蛋白(Bone sialoprotein,BSP)和白细胞介素8(Interleukin 8,IL-8)基因表达的调节。方法 10mg/L P.g.LPS处理第4-5代体外培养的hPDLFs不同时间(1、4、8、12、24小时)后,采用实时荧光定量PCR(Real-time PCR)检测骨唾液酸蛋白(BSP)和IL-8基因的表达水平。结果 10mg/L P.g.LPS作用hPDLFs 1、4小时后BSP mRNA的表达水平稍有下降(P>0.05),并在刺激8、12、24小时后BSP mRNA的表达水平显著下降(P<0.01);此外10mg/L P.g.LPS明显上调hPDLFs中IL-8 mRNA表达水平,在处理8h时刺激作用最为明显,达到高峰(P<0.01)。结论高浓度(10mg/L)P.g.LPS对hPDLFs的BSP基因表达有抑制作用,而对IL-8基因表达有增强作用。Objective To investigate the regulation of gene expression of bone sialoprotein (BSP) hand Interleukin 8 (IL-8) by high concentration of Porphyromonas gingivalis lipopolysaecharide (P.g.LPS) in human periodontal ligament fibroblasts (hPDLFs). Methods hPDLFs cells were cultured in 10mg/L P.g. LPS for time course (1,4,8,12,24h), total RNA were extracted, and then BSPand IL-8 mRNA levels were observed by Real-time PCR. Results l0mg/L P.g. LPS decreased the BSP mRNA expression in hPDLFs after stimulation for 8h (P〈0.01), while IL- 8 mRNA levels were up-regulated by 10mg/L P.g. LPS at 8h (P〈0.01). Conclusion The effects of high concentration of P.g. LPS (l0mg/L) on the BSP mRNA levels in hPDLFs were suppressed, whereas on the IL-8 mRNA expression were enhanced.
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