Guan Su-Min, He Jian-Jun, Zhang Ming, Shu Lei
Department of Preventive Dentistry and Infection Control Office, School of Stomatology, The Fourth Military Medical University, Xi'an, China.
FEMS Immunol Med Microbiol. 2011 Jun;62(1):91-100. doi: 10.1111/j.1574-695X.2011.00789.x. Epub 2011 Mar 8.
Prevotella intermedia is an important periodontal pathogen that induces various inflammatory and immune responses. In this study, we investigated the effects of P. intermedia on the plasminogen system in human periodontal ligament (hPDL) cells and explored the signaling pathways involved. Using semi-quantitative reverse transcription (RT)-PCR and quantitative real-time RT-qPCR, we demonstrated that P. intermedia challenge increased tissue-type plasminogen activator (tPA) and plasminogen activator inhibitor (PAI)-2 expression in a concentration- and time-dependent manner, but exerted no influence on urokinase-type plasminogen activator and PAI-1mRNA expression in hPDL cells. Prevotella intermedia stimulation also enhanced tPA protein secretion as confirmed by enzyme-linked immunosorbent assay. Western blot results revealed that P. intermedia treatment increased phosphorylation of extracellular signal-regulated kinase (ERK), c-Jun N-terminal kinase (JNK) and p38 kinase (p38). ERK, JNK and protein kinase C inhibitors significantly attenuated the P. intermedia-induced tPA and PAI-2 expression. Furthermore, p38 and phosphatidylinositol 3-kinase inhibitors markedly decreased PAI-2 expression, whereas they showed no or little inhibition on tPA expression. In contrast, inhibition of protein kinase A greatly enhanced the upregulatory effect of P. intermedia on tPA and PAI-2 expression. Our results suggest that P. intermedia may contribute to periodontal tissue destruction by upregulating tPA and PAI-2 expression in hPDL cells via multiple signaling pathways.
中间普氏菌是一种重要的牙周病原体,可引发多种炎症和免疫反应。在本研究中,我们调查了中间普氏菌对人牙周膜(hPDL)细胞中纤溶酶原系统的影响,并探索了其中涉及的信号通路。通过半定量逆转录(RT)-PCR和定量实时RT-qPCR,我们证明中间普氏菌刺激以浓度和时间依赖性方式增加了组织型纤溶酶原激活物(tPA)和纤溶酶原激活物抑制剂(PAI)-2的表达,但对hPDL细胞中尿激酶型纤溶酶原激活物和PAI-1mRNA表达没有影响。酶联免疫吸附测定证实,中间普氏菌刺激还增强了tPA蛋白的分泌。蛋白质印迹结果显示,中间普氏菌处理增加了细胞外信号调节激酶(ERK)、c-Jun氨基末端激酶(JNK)和p38激酶(p38)的磷酸化。ERK、JNK和蛋白激酶C抑制剂显著减弱了中间普氏菌诱导的tPA和PAI-2表达。此外,p38和磷脂酰肌醇3激酶抑制剂显著降低了PAI-2表达,而它们对tPA表达没有或几乎没有抑制作用。相反,抑制蛋白激酶A大大增强了中间普氏菌对tPA和PAI-2表达的上调作用。我们的结果表明,中间普氏菌可能通过多种信号通路上调hPDL细胞中tPA和PAI-2的表达,从而导致牙周组织破坏。