Zhao L, Chen J, Cheng L, Wang X, Du J, Wang F, Peng Z
Department of Operative Dentistry and Endodontics, Guanghua School of Stomatology, Hospital of Stomatology, Sun Yat-sen University, Guangzhou, China.
Int Endod J. 2014 Feb;47(2):163-72. doi: 10.1111/iej.12127. Epub 2013 May 25.
To investigate the influence of Enterococcus faecalis lipoteichoic acid (LTA) on the key bone resorption-regulating proteins, receptor activator of nuclear factor-κB ligand (RANKL) and osteoprotegerin (OPG) in human periodontal ligament fibroblasts (PDL cells).
Periodontal ligament cells were subjected to various concentrations of LTA. Cell viability was then determined by methyl thiazolyl tetrazolium (MTT) assay, whilst the expression levels of RANKL and OPG were investigated by enzyme-linked immunosorbent assay (ELISA) and Western blotting. The effect of the inhibitors [IL-1 receptor-associated kinase (IRAK)-1/4, p38 mitogen-activated protein kinase (MAPK) (SB203580)] on LTA-stimulated RANKL/OPG activation was examined. Cell viability and RANKL/OPG ratio in PDL cells were also analysed by MTT assay and Western blotting. Data were analysed using one-way anova or t-test at a significance level of P = 0.05.
Cell viability was reduced significantly in the LTA group in a dose-dependent fashion (P < 0.05). In addition, LTA was found to upregulate the protein expression of RANKL, OPG and their relative ratio in PDL cells (P < 0.05). The optimal concentration of LTA used in PDL cells was determined to be 10 μg mL(-1) . Following IRAK1/4 and p38MAPK inhibition, LTA-stimulated increases of RANKL/OPG ratio were significantly reduced (P < 0.05).
Enterococcus faecalis LTA could upregulate the expression of RANKL and OPG at different rates, suggesting a potential role for LTA in the bone resorption process of refractory apical periodontitis through the regulation of RANKL and OPG. In addition, IRAK1/4 and p38MAPK signalling involving RANKL/OPG may contribute to inflammatory responses from PDL cells.
研究粪肠球菌脂磷壁酸(LTA)对人牙周膜成纤维细胞(PDL细胞)中关键骨吸收调节蛋白——核因子κB受体活化因子配体(RANKL)和骨保护素(OPG)的影响。
将牙周膜细胞暴露于不同浓度的LTA中。然后通过甲基噻唑基四氮唑(MTT)法测定细胞活力,同时采用酶联免疫吸附测定(ELISA)和蛋白质印迹法研究RANKL和OPG的表达水平。检测抑制剂[白细胞介素-1受体相关激酶(IRAK)-1/4、p38丝裂原活化蛋白激酶(MAPK)(SB203580)]对LTA刺激的RANKL/OPG活化的影响。还通过MTT法和蛋白质印迹法分析PDL细胞中的细胞活力和RANKL/OPG比值。数据采用单因素方差分析或t检验进行分析,显著性水平为P = 0.05。
LTA组细胞活力呈剂量依赖性显著降低(P < 0.05)。此外,发现LTA可上调PDL细胞中RANKL、OPG的蛋白表达及其相对比值(P < 0.05)。确定PDL细胞中使用的LTA最佳浓度为10μg mL(-1)。在抑制IRAK1/4和p38MAPK后,LTA刺激的RANKL/OPG比值增加显著降低(P < 0.05)。
粪肠球菌LTA可不同程度地上调RANKL和OPG的表达,提示LTA可能通过调节RANKL和OPG在难治性根尖周炎的骨吸收过程中发挥潜在作用。此外,涉及RANKL/OPG的IRAK1/4和p38MAPK信号传导可能促成PDL细胞的炎症反应。