BACKGROUND:An impairment of the intestinal barrier function is one of the major characteristics of Crohn's disease (CD). This study aimed to evaluate the impact of autophagy induction by rapamycin on the intestinal epithelial barrier function in CD model mice. METHODS:IL-10 knockout (IL-10 KO) mice were used as the human CD models in this study. All the mice were randomly assigned into four groups, (a) wild-type (WT) group; (b) IL-10 KO group; (c) IL-10 KO + rapamycin group and (d) IL-10 KO + 3-methyladenine (3-MA), containing 6 mice in each group. The disease activity index (DAI), histology, pro-inflammatory cytokines and chemotactic factors in colon tissues, intestinal and colonic permeability, distributions and expressions of tight junction (TJ) proteins, epithelial apoptosis of mice in four groups were evaluated and compared. RESULTS:Autophagy induction by rapamycin treatment ameliorated DAI and histological colitis, decreased pro-inflammatory cytokines (TNF-α, IFN-γ and IL-17) and chemotactic factors (CXCL-1 and CXCL-2), decreased intestinal and colonic permeability, improved the distribution and expression of TJ proteins in IL-10 KO mice. CONCLUSION:Autophagy induction by rapamycin significantly improved intestinal barrier function and protected IL-10 KO mice from the experimental chronic colitis.

译文

背景:肠道屏障功能的损害是克罗恩病(CD)的主要特征之一。这项研究旨在评估雷帕霉素诱导的自噬对CD模型小鼠肠上皮屏障功能的影响。
方法:以IL-10基因敲除小鼠(IL-10 KO)作为人类CD模型。将所有小鼠随机分为四组,(a)野生型(WT)组;(b)野生型(WT)组。 (b)IL-10 KO组; (c)IL-10 KO雷帕霉素组和(d)IL-10 KO 3-甲基腺嘌呤(3-MA),每组6只小鼠。评估并比较了四组小鼠的疾病活动指数(DAI),组织学,结肠组织中的促炎细胞因子和趋化因子,肠和结肠通透性,紧密连接(TJ)蛋白的分布和表达,小鼠上皮细胞凋亡。
结果:雷帕霉素诱导的自噬改善了DAI和组织性结肠炎,降低了促炎细胞因子(TNF-α,IFN-γ和IL-17)和趋化因子(CXCL-1和CXCL-2),降低了肠道和结肠的通透性,改善了IL-10 KO小鼠中TJ蛋白的分布和表达。
结论:雷帕霉素自噬诱导显着改善肠屏障功能,并保护IL-10 KO小鼠免受实验性慢性结肠炎的侵害。

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