Feng Qin, Zhang Feng-qiu, Sun Zheng, Zhang Xin-yan, Liu Jie
Department of Periodontics and Mucosa Disease, Capital Medical University School of Stomatology, Beijing 100050, China.
Zhonghua Kou Qiang Yi Xue Za Zhi. 2012 Oct;47(10):605-9. doi: 10.3760/cma.j.issn.1002-0098.2012.10.007.
To evaluate the effects of sonicated extracts of Porphyromonas gingivalis (Pg) on receptor activator of NF-κB ligand (RANKL) and osteoprotegerin (OPG) expression in human periodontal ligament cells (HPDLC) and the effect of Pg on bone resorption in periodontitis.
HPDLC were exposed to 25, 50 mg/L sonicated extracts of Pg for 6 h, HPDLC without treatment served as control. The expression of RANKL-OPG mRNA and protein were examined by real time polymerase chain reaction and Western blotting. OPG protein in the supernatant was examined by enzyme linked immunosorbent assay (ELISA). The data were statistically analyzed by SPSS 13.0 and one-way analysis of variance (ANOVA).
When HPDLC were exposed to sonicated extracts of Pg, the expression of RANKL mRNA and protein in 25 mg/L and 50 mg/L groups were higher than that of control group (P < 0.05), the expression of OPG mRNA in 50 mg/L group (0.087 ± 0.021) was lower than that of control group (0.240 ± 0.019) (P < 0.05), and OPG protein in 25 mg/L and 50 mg/L groups (0.813 ± 0.007, 0.398 ± 0.009) was lower than that of control group (1.131 ± 0.005) (P < 0.01). OPG protein expression in the supernatant was not significantly different between experimental group and control group.
Sonicated extracts of Pg exposed to HPDLC can up-regulate RANKL expression, down-regulate OPG expression and influence bone metabolism.
评估牙龈卟啉单胞菌(Pg)超声提取物对人牙周膜细胞(HPDLC)中核因子κB受体活化因子配体(RANKL)和骨保护素(OPG)表达的影响,以及Pg对牙周炎骨吸收的影响。
将HPDLC暴露于25、50mg/L的Pg超声提取物中6小时,未处理的HPDLC作为对照。通过实时聚合酶链反应和蛋白质印迹法检测RANKL - OPG mRNA和蛋白的表达。采用酶联免疫吸附测定(ELISA)检测上清液中的OPG蛋白。数据采用SPSS 13.0软件进行统计学分析,并进行单因素方差分析(ANOVA)。
当HPDLC暴露于Pg超声提取物时,25mg/L和50mg/L组中RANKL mRNA和蛋白的表达高于对照组(P < 0.05),50mg/L组中OPG mRNA的表达(0.087±0.021)低于对照组(0.240±0.019)(P < 0.05),25mg/L和50mg/L组中OPG蛋白(0.813±0.007,0.398±0.009)低于对照组(1.131±0.005)(P < 0.01)。实验组和对照组上清液中OPG蛋白表达无显著差异。
暴露于HPDLC的Pg超声提取物可上调RANKL表达,下调OPG表达并影响骨代谢。