Department of Periodontology, Faculty of Dentistry, Khon Kaen University, Khon Kaen, Thailand.
J Periodontol. 2013 Jul;84(7):1010-8. doi: 10.1902/jop.2012.120362. Epub 2012 Sep 24.
Toll-like receptors (TLRs) play pivotal roles in host immune responses and have been suggested to be involved in the development of many infectious diseases. In this study, the mRNA expression levels of TLR2, TLR4, and TLR9 and their relationship with periodontopathic bacteria in periodontal tissue are examined. Furthermore, the mechanism of TLR induction by Porphyromonas gingivalis is investigated in human gingival fibroblasts (HGFs).
Gingival tissue and subgingival plaque samples were collected from 19 patients with chronic periodontitis (CP) and 16 control individuals without periodontitis. Gene expression levels in the tissues and in HGFs were analyzed by reverse transcription-polymerase chain reaction (RT-PCR). The numbers of periodontopathic bacteria were determined by quantitative real-time PCR.
The expression levels of TLR2 and TLR9 were significantly higher in the tissues of patients with CP compared to the tissues of control individuals. The mRNA levels of TLR2 and TLR9, but not TLR4, were positively correlated with the number of P. gingivalis in subgingival plaque. P. gingivalis sonicated extract, P. gingivalis lipopolysaccharide, P. gingivalis DNA, and tumor necrosis factor-α(TNF-α) could significantly upregulate the mRNA expression of TLR2 in HGFs. Furthermore, P. gingivalis-mediated TLR2 expression was suppressed by TNF-α antibody.
This study suggests that P. gingivalis infection induces TLR2 and TLR9 upregulation in patients with CP. P. gingivalis-induced TLR2 expression in HGFs is partially dependent on TNF-α and may lead to sensitization of HGFs to bacterial components encountered in the periodontal microenvironment.
Toll 样受体(TLRs)在宿主免疫反应中发挥关键作用,并且被认为与许多传染病的发展有关。在这项研究中,检查了 TLR2、TLR4 和 TLR9 的 mRNA 表达水平及其与牙周组织中牙周病细菌的关系。此外,还研究了牙龈卟啉单胞菌诱导 TLR 的机制在人牙龈成纤维细胞(HGFs)中。
从 19 名慢性牙周炎(CP)患者和 16 名无牙周炎的对照个体中收集牙龈组织和龈下菌斑样本。通过逆转录-聚合酶链反应(RT-PCR)分析组织和 HGFs 中的基因表达水平。通过定量实时 PCR 确定牙周病细菌的数量。
与对照组相比,CP 患者组织中 TLR2 和 TLR9 的表达水平显着升高。TLR2 和 TLR9 的 mRNA 水平,但不是 TLR4,与龈下菌斑中 P. gingivalis 的数量呈正相关。牙龈卟啉单胞菌超声提取物、牙龈卟啉单胞菌脂多糖、牙龈卟啉单胞菌 DNA 和肿瘤坏死因子-α(TNF-α)均可显着上调 HGFs 中 TLR2 的 mRNA 表达。此外,TNF-α 抗体可抑制牙龈卟啉单胞菌介导的 TLR2 表达。
本研究表明,P. gingivalis 感染诱导 CP 患者 TLR2 和 TLR9 的上调。HGFs 中 P. gingivalis 诱导的 TLR2 表达部分依赖于 TNF-α,并且可能导致 HGFs 对牙周微环境中遇到的细菌成分敏感。