首页> 外文期刊>Journal of periodontal research >Elevated mRNA expression for supervillin and vascular endothelial growth factor in human neutrophils stimulated with lipopolysaccharide from Porphyromonas gingivalis.
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Elevated mRNA expression for supervillin and vascular endothelial growth factor in human neutrophils stimulated with lipopolysaccharide from Porphyromonas gingivalis.

机译:牙龈卟啉单胞菌脂多糖刺激人嗜中性粒细胞中supervillin和血管内皮生长因子的mRNA表达升高。

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Differential gene expression was examined in human neutrophils stimulated with lipopolysaccharide from Porphyromonas gingivalis (P. gingivalis-LPS) using RNA fingerprinting by arbitrarily primed polymerase chain reaction (RAP-PCR). LPS from Escherichia coli (E. coli-LPS) was used as control. More than 200 differently expressed transcripts were found in 8 subjects showing differential regulation at the transcriptional level. Densitometric analyses revealed that 42-100 genes were upregulated, while 53-116 genes were downregulated by P. gingivalis-LPS compared with E. coli-LPS. The results of sequencing identification showed the presence of supervillin (SVIL) and vascular endothelial growth factor (VEGF) genes in the clones which were upregulated by P. gingivalis-LPS. Consequently, semiquantitative analyses proved that the level of mRNA for SVIL and VEGF were significantly higher in P. gingivalis-LPS-stimulated neutrophils than in other bacterial (E. coli, Actinobacillus actinomycetemcomitans, Prevotella intermedia) LPS- or synthetic lipid A-stimulated neutrophils. Our findings suggest that an elevated mRNA expression for SVIL could be associated with impaired function of neutrophils when stimulated by P. gingivalis-LPS. Further, the VEGF mRNA over-expression might be related to the pathogenesis of P. gingivalis-associated periodontitis. The RAP-PCR technique used in this study enabled us to identify a number of P. gingivalis-LPS regulated genes which hitherto have not been reported.
机译:通过任意引发的聚合酶链反应(RAP-PCR)使用RNA指纹技术,检测了来自牙龈卟啉单胞菌(P. gingivalis-LPS)的脂多糖刺激的人中性粒细胞的差异基因表达。来自大肠杆菌的LPS(大肠杆菌-LPS)用作对照。在8位受试者中发现了200多种不同表达的转录本,显示出在转录水平上的差异调控。光密度分析表明,与大肠杆菌-LPS相比,牙龈丙酸杆菌-LPS上调了42-100个基因,而53-116个基因下调。测序鉴定的结果表明,在由牙龈卟啉单胞菌-LPS上调的克隆中存在supervillin(SVIL)和血管内皮生长因子(VEGF)基因。因此,半定量分析证明,牙龈卟啉单胞菌-LPS刺激的中性粒细胞中SVIL和VEGF的mRNA水平明显高于其他细菌(大肠杆菌,放线菌,放线杆菌,中间小球藻),LPS或合成的脂质A刺激的中性粒细胞。 。我们的发现表明,当由牙龈卟啉单胞菌-LPS刺激时,SVIL的mRNA表达升高可能与中性粒细胞功能受损有关。此外,VEGF mRNA的过度表达可能与牙龈卟啉单胞菌相关的牙周炎的发病机制有关。这项研究中使用的RAP-PCR技术使我们能够鉴定出迄今尚未报道的许多P. gingivalis-LPS调控基因。

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