Liu Chang, Jing Ke
Department of Pediatrics, Fourth Affiliated Hospital of China Medical University, Shenyang 110032, China.
Zhongguo Dang Dai Er Ke Za Zhi. 2018 Feb;20(2):158-163. doi: 10.7499/j.issn.1008-8830.2018.02.015.
To investigate the effects of Toll-like receptor blockers TLR2-Ab and TLR4-Ab on the tight junction protein ZO-1 in intestinal epithelial cells in mice, as well as their effects on nuclear factor-kappa B (NF-κB) and tumor necrosis factor-α (TNF-α).
A total of 32 BALB/C mice were divided into control group, model group, TLR4 treatment group, and TLR2 treatment group, with 8 mice in each group. A mouse model of endotoxemia was established by intraperitoneal injection of lipopolysaccharide. The mice in the TLR4 treatment group and the TLR2 treatment group were given intraperitoneal injection of TLR4 antibody and TLR2 antibody (10 μg each mouse), respectively, and those in the control group were given normal saline. The distal small intestinal tissue was collected, and RT-PCR and immunohistochemistry were used to measure the mRNA and protein expression of ZO-1, NF-κBp65, and TNF-α.
Compared with the control group, the model group had significantly lower mRNA and protein expression of ZO-1 and significantly higher mRNA expression of NF-κBp65 and TNF-α (P<0.05). Compared with the model group, the TLR4 treatment group and the TLR2 treatment group had significantly higher mRNA and protein expression of ZO-1 and significantly lower mRNA and protein expression of NF-κBp65 and TNF-α (P<0.05). There were no significant differences in the mRNA and protein expression of ZO-1, NF-κBp65, and TNF-α between the TLR4 treatment group and the TLR2 treatment group (P>0.05).
Anti-TLR2 and anti-TLR4 monoclonal antibodies can reduce the activation of nuclear transcription factors, inhibit the secretion of inflammatory factors, and protect tight junction protein, which is expected to provide new ideas for the treatment of enterogenous infectious diseases.
探讨Toll样受体阻断剂TLR2抗体和TLR4抗体对小鼠肠上皮细胞紧密连接蛋白ZO - 1的影响,以及对核因子-κB(NF-κB)和肿瘤坏死因子-α(TNF-α)的影响。
将32只BALB/C小鼠分为对照组、模型组、TLR4治疗组和TLR2治疗组,每组8只。通过腹腔注射脂多糖建立内毒素血症小鼠模型。TLR4治疗组和TLR2治疗组小鼠分别腹腔注射TLR4抗体和TLR2抗体(每只小鼠10μg),对照组小鼠给予生理盐水。收集远端小肠组织,采用逆转录-聚合酶链反应(RT-PCR)和免疫组织化学法检测ZO - 1、NF-κBp65和TNF-α的mRNA和蛋白表达。
与对照组相比,模型组ZO - 1的mRNA和蛋白表达显著降低,NF-κBp65和TNF-α的mRNA表达显著升高(P<0.05)。与模型组相比,TLR4治疗组和TLR2治疗组ZO - 1的mRNA和蛋白表达显著升高,NF-κBp65和TNF-α的mRNA和蛋白表达显著降低(P<0.05)。TLR4治疗组和TLR2治疗组之间ZO - 1、NF-κBp65和TNF-α的mRNA和蛋白表达无显著差异(P>0.05)。
抗TLR2和抗TLR4单克隆抗体可降低核转录因子的激活,抑制炎性因子的分泌,保护紧密连接蛋白,有望为肠源性感染性疾病的治疗提供新思路。