Yang Xia, Gao Xian-Chun, Liu Jun, Ren Hong-Yu
Xia Yang, Xian-Chun Gao, Jun Liu, Hong-Yu Ren, Division of Gastroenterology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, Hubei Province, China.
World J Gastroenterol. 2017 Jul 14;23(26):4744-4751. doi: 10.3748/wjg.v23.i26.4744.
To investigate toll-like receptor 2 (TLR2) and TLR4 expression, following bifidobacteria and low-dose EPEC endotoxin treatment, and intestinal barrier function in rat intestinal epithelial cell18 (IEC18).
Six experimental groups were established - normal control, EPEC, (), , , and groups. Optimal EPEC endotoxin concentration, bifidobacteria fold dilution, and treatment duration were determined. Quantitative real-time polymerase chain reaction and western blot, respectively, were conducted to detect TLR2 and TLR4 mRNA and protein expression in IEC-18 cells. Transepithelial electrical resistance (TEER) was measured by the EVOM chopstick voltohmmeter in each group. All experiments were conducted in triplicate and data were analyzed on SPSS 16.
TLR2 and TLR4 mRNA and protein expression in the EPEC group were significantly higher than in the control group ( < 0.05). TLR2 mRNA and protein expression in the , and groups were significantly lower than in the normal control group ( < 0.05). TLR4 mRNA and protein expression in the and groups were significantly lower than in normal controls ( < 0.05). In addition, the TEER in , , , and groups were decreased by 19%, 18%, 23% and 23%, respectively, after 120 min of intervention, as compared to the control group. However, the TEER in the EPEC group was significantly decreased by 67% in comparison to the normal control group ( < 0.05).
Bifidobacteria protect IEC-18 cells against injury by down-regulating TLR2 and TLR4 expression and enhance intestinal barrier function to protect the intestinal epithelial cells from pathogenic invasion.
研究双歧杆菌和低剂量肠致病性大肠杆菌(EPEC)内毒素处理后,大鼠肠上皮细胞18(IEC18)中Toll样受体2(TLR2)和TLR4的表达以及肠道屏障功能。
建立六个实验组——正常对照组、EPEC组、()组、组、组和组。确定最佳的EPEC内毒素浓度、双歧杆菌稀释倍数和处理持续时间。分别采用定量实时聚合酶链反应和蛋白质印迹法检测IEC-18细胞中TLR2和TLR4的mRNA和蛋白表达。用EVOM筷子伏特计测量每组的跨上皮电阻(TEER)。所有实验均重复三次,数据用SPSS 16进行分析。
EPEC组中TLR2和TLR4的mRNA和蛋白表达显著高于对照组(P<0.05)。组、组和组中TLR2的mRNA和蛋白表达显著低于正常对照组(P<0.05)。组和组中TLR4的mRNA和蛋白表达显著低于正常对照组(P<0.05)。此外,干预120分钟后,组、组、组和组的TEER分别比对照组降低了19%、18%、23%和23%。然而,与正常对照组相比,EPEC组的TEER显著降低了67%(P<0.05)。
双歧杆菌通过下调TLR2和TLR4的表达保护IEC-18细胞免受损伤,并增强肠道屏障功能以保护肠上皮细胞免受病原体侵袭。