Institute of Oral Biology, Center of Dental and Oral Medicine and Cranio-Maxillofacial Surgery, University of Zürich, Plattenstrasse 11, Zürich, Switzerland.
Inflammation. 2011 Apr;34(2):133-8. doi: 10.1007/s10753-010-9216-1.
Porphyromonas gingivalis is an oral pathogen highly implicated in chronic periodontitis, a disease characterized by inflammatory destruction of the tooth-supporting alveolar bone and eventually, tooth loss. T-cell innate immune responses are actively involved in this pathological process. Receptor activator of NF-κB Ligand (RANKL) is a cytokine that stimulates bone resorption, while its soluble decoy receptor osteoprotegerin (OPG) blocks its action. This study aimed to investigate in Jurkat T-cells the effects of P. gingivalis on the RANKL-OPG system and the major inflammatory mediator of bone resorption prostaglandin E(2) (PGE(2)). P. gingivalis caused concentration-dependent up-regulation of RANKL gene expression and protein production, assessed by quantitative PCR and ELISA, respectively. PGE(2) production was also enhanced. However, OPG was not detected. In conclusion, P. gingivalis induces RANKL and PGE(2) in T-cells, potentially favoring bone resorption. These T-cell responses to P. gingivalis may contribute to the pathogenesis of inflammatory alveolar bone destruction occurring in chronic periodontitis.
牙龈卟啉单胞菌是一种口腔病原体,高度参与慢性牙周炎,这是一种以支持牙齿的牙槽骨炎症性破坏为特征的疾病,最终导致牙齿脱落。T 细胞先天免疫反应积极参与这一病理过程。核因子-κB 受体激活剂配体(RANKL)是一种刺激骨吸收的细胞因子,而其可溶性诱饵受体骨保护素(OPG)则阻断其作用。本研究旨在探讨牙龈卟啉单胞菌对 Jurkat T 细胞中 RANKL-OPG 系统和骨吸收主要炎症介质前列腺素 E2(PGE2)的影响。通过定量 PCR 和 ELISA 分别评估,牙龈卟啉单胞菌导致 RANKL 基因表达和蛋白产生的浓度依赖性上调。PGE2 的产生也增强了。然而,未检测到 OPG。总之,牙龈卟啉单胞菌诱导 T 细胞中 RANKL 和 PGE2 的产生,可能有利于骨吸收。T 细胞对牙龈卟啉单胞菌的这些反应可能有助于慢性牙周炎中发生的炎症性牙槽骨破坏的发病机制。