Department of Preventive Dentistry, School of Stomatology, Fourth Military Medical University, Xi'an, 710032, China.
J Dent Res. 2011 Jan;90(1):121-7. doi: 10.1177/0022034510382545. Epub 2010 Nov 5.
Prostaglandin E(2) (PGE(2)) plays important roles in the bone resorption of inflammatory diseases such as rheumatoid arthritis and periodontitis via specific prostaglandin receptors (i.e., EP1-EP4). In this study, the authors examined whether Prevotella intermedia regulates PGE(2) production and EP expression in human periodontal ligament fibroblasts (hPDLs); they also explored the potential signaling pathways involved in PGE(2) production. P. intermedia induced PGE(2) production and cyclooxygenase-2 (COX-2) expression in a dose- and time-dependent manner. Indomethacin and NS-398 completely abrogated the P. intermedia-induced PGE(2) production without modulating COX-2 expression. Specific inhibitors of extracellular signal-regulated kinase, c-Jun N-terminal kinase, p38, phosphatidylinositol 3-kinase, and protein kinase C--but not c-AMP and protein kinase A--significantly attenuated the P. intermedia-induced COX-2 and PGE(2) expression. P. intermedia reduced EP1 expression in a concentration- and time-dependent manner. The results indicate that the COX-2-dependent induction of PGE(2) by P. intermedia in hPDLs is mediated by multiple signaling pathways.
前列腺素 E(2)(PGE(2))通过特定的前列腺素受体(即 EP1-EP4)在类风湿关节炎和牙周炎等炎症性疾病的骨吸收中发挥重要作用。在这项研究中,作者研究了中间普氏菌是否调节人牙周膜成纤维细胞(hPDLs)中 PGE(2)的产生和 EP 表达;他们还探讨了参与 PGE(2)产生的潜在信号通路。中间普氏菌以剂量和时间依赖的方式诱导 PGE(2)产生和环氧化酶-2(COX-2)表达。吲哚美辛和 NS-398 完全阻断了中间普氏菌诱导的 PGE(2)产生,而不调节 COX-2 表达。细胞外信号调节激酶、c-Jun N-末端激酶、p38、磷脂酰肌醇 3-激酶和蛋白激酶 C 的特异性抑制剂——而不是 c-AMP 和蛋白激酶 A——显著减弱了中间普氏菌诱导的 COX-2 和 PGE(2)表达。中间普氏菌以浓度和时间依赖的方式降低 EP1 表达。结果表明,中间普氏菌在 hPDLs 中通过多种信号通路诱导 COX-2 依赖性 PGE(2)产生。