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Regulation of RANKL and OPG gene expression in human gingival fibroblasts and periodontal ligament cells by Porphyromonas gingivalis: a putative role of the Arg-gingipains

机译:牙龈卟啉单胞菌对人牙龈成纤维细胞和牙周膜细胞中RANKL和OPG基因表达的调节:Arg-牙龈蛋白酶的推定作用

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摘要

Porphyromonas gingivalis is highly implicated in the pathogenesis of periodontitis, which is characterized by the destruction of periodontal connective tissues and the supporting alveolar bone. Receptor Activator of NF-kappaB Ligand (RANKL) stimulates bone resorption, whereas osteoprotegerin (OPG) blocks its action, and this bi-molecular system is implicated in periodontitis. The aim of this work was (a) to investigate the regulation of RANKL and OPG gene expression in human periodontal ligament (PDL) cells and gingival fibroblasts (GF), in response to P. gingivalis culture supernatants, by quantitative real-time PCR and (b) to attempt to identify putative virulence factors involved in this process. The results indicated that P. gingivalis induced RANKL and reduced OPG mRNA expression by the studied cells, resulting in an increased RANKL/OPG expression ratio. Heat-inactivation of P. gingivalis resulted in significant reduction of RANKL mRNA expression. A Lys-gingipain mutant strain did not affect, whereas an Arg-gingipain mutant strain further enhanced RANKL mRNA expression, compared to their parental wild-type strain. In conclusion, P. gingivalis up-regulates the RANKL/OPG expression ratio in GF and PDL cells, denoting an enhanced osteoclastogenic potential by the cells. The component mainly responsible for RANKL induction appears to be proteinaceous, and it may be regulated by the Arg-gingipains.
机译:牙龈卟啉单胞菌与牙周炎的发病机理高度相关,其特征在于牙周结缔组织和支持牙槽骨的破坏。 NF-κB配体的受体激活剂(RANKL)刺激骨吸收,而骨保护素(OPG)阻止其作用,这种双分子系统与牙周炎有关。这项工作的目的是(a)通过定量实时PCR和逆转录分析技术研究人牙周膜培养物上清液对人牙周膜(PDL)细胞和牙龈成纤维细胞(GF)中RANKL和OPG基因表达的调控。 (b)试图确定此过程中涉及的推定毒力因子。结果表明,牙龈卟啉单胞菌诱导RANKL并降低了所研究细胞的OPG mRNA表达,从而导致RANKL / OPG表达比增加。牙龈卟啉单胞菌的热失活导致RANKL mRNA表达显着降低。与它们的亲本野生型菌株相比,Lys-gingipain突变菌株没有影响,而Arg-gingipain突变菌株进一步增强了RANKL mRNA表达。总之,牙龈卟啉单胞菌上调了GF和PDL细胞中RANKL / OPG的表达比例,表明该细胞增强了破骨细胞的潜力。主要负责RANKL诱导的成分似乎是蛋白质,可能受Arg-gingipains调节。

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