Jin Luyuan, Luo Xiaoliang, Jiang Yan, Xie Xiaoli
Dept. of Stomatology, Xiangya Hospital, Central-south University, Changsha 410008, China.
Hua Xi Kou Qiang Yi Xue Za Zhi. 2012 Feb;30(1):93-6.
To investigate the expression of Toll like receptor 2 (TLR2) and interleukin-1 beta (IL-1 beta) of cultured human periodontal ligament cells (HPDLCs) activated by Enterococcus faecalis (E. faecalis) lipoteichoic acid (LTA).
HPDLCs that were obtained from the periodontal tissues of healthy humans were maintained in proper condition. Flow cytometry was used to detect the expression of TLR2 on normal HPDLCs and infectious HPDLCs which were incubated with 0.1, 1, 10 microg mL(-1) E. faecalis LTA for 24 h. IL-1 beta was detected by enzyme linked immunosorbent assay (ELISA) after incubating with LTA of the above concentration for 12, 24 and 48 h or pretreated with TLR2 neutralizing antibody for 1 h and then co-cultured with 1 microg mL(-1) LTA for 24 h.
E. faecalis LTA promoted the expression of TLR2 in normal HPDLCs. The difference had statistical significance (P<0.05). IL-1 beta secretion could be detected 12h after stimulation with LTA and increasingly escalate within 48h (P<0.05). TLR2 neutralizing antibody had no evident effect on IL-1 beta generation stimulating by E. faecalis LTA.
E. faecalis LTA can increase the expression of TLR2 and IL-1 beta in normal HPDLCs.
研究粪肠球菌脂磷壁酸(LTA)激活培养的人牙周膜细胞(HPDLCs)后Toll样受体2(TLR2)和白细胞介素-1β(IL-1β)的表达。
从健康人牙周组织获取HPDLCs并妥善培养。采用流式细胞术检测正常HPDLCs以及分别用0.1、1、10μg/mL粪肠球菌LTA孵育24小时后的感染性HPDLCs中TLR2的表达。在分别用上述浓度的LTA孵育12、24和48小时后,或先用TLR2中和抗体预处理1小时,再与1μg/mL LTA共培养24小时后,通过酶联免疫吸附测定(ELISA)检测IL-1β。
粪肠球菌LTA促进正常HPDLCs中TLR2的表达。差异具有统计学意义(P<0.05)。LTA刺激12小时后可检测到IL-1β分泌,并在48小时内逐渐增加(P<0.05)。TLR2中和抗体对粪肠球菌LTA刺激产生IL-1β无明显影响。
粪肠球菌LTA可增加正常HPDLCs中TLR2和IL-1β的表达。