Department of Nephrology,; National Center for Children's Health (Beijing), Beijing, China; Key Laboratory of Chronic Kidney Disease and Blood Purification in Childhood (Beijing), Beijing, China; Key Laboratory of Major Diseases in Children, Ministry of Education, Beijing, China.
Department of Traditional Chinese Medicine, Beijing Children's Hospital, Capital Medical University, Beijing, China; National Center for Children's Health (Beijing), Beijing, China.
Am J Med Sci. 2020 Mar;359(3):168-176. doi: 10.1016/j.amjms.2019.11.011. Epub 2019 Nov 30.
Intestinal-barrier damage plays an important pathogenic role in immunoglobulin A nephropathy (IgAN). In this study, we explored the characteristics of the intestinal barrier in rats with IgAN.
We randomly divided 17 Sprague Dawley (SD) male rats into a normal control group (NC; n = 9) and an IgAN model group (n = 8). Feces in the distal ileum were taken for intestinal-microbiota 16sDNA sequencing. We also took a segment of terminal ileum to analyze intestinal morphology and to detect mRNA and protein expression of the tight-junction proteins zonula occludens-1 (ZO-1) and occludin (OCLN), as well as of mucin 2 (MUC2). We then measured levels of serum diamine oxidase (DAO) and D-lactic acid (D-LA), the biomarkers of intestinal permeability.
Compared with the NC group, mRNA expression levels of ZO-1 (t = 4.216, P = 0.0007), OCLN (t = 2.413, P = 0.029) and MUC2 (t = 0.859, P < 0.0001) were significantly decreased in the IgAN model group. Protein expression of ZO-1 (t = 7.349, P < 0.0001) and OCLN (t = 6.367, P < 0.0001) was also decreased in the IgAN model group. Conversely, serum DAO (t = 3.758, P = 0.0024) and D-LA (t = 2.246, P = 0.0427) levels increased in this group. At the genus level, the relative abundance of Ruminococcus2 (P = 0.0086) was increased in the IgAN model group.
Decreased expression of ZO-1, OCLN and MUC2, plus intestinal-microbiota dysbiosis, are associated with intestinal-barrier damage in IgAN rats.
肠屏障损伤在免疫球蛋白 A 肾病(IgAN)中起着重要的致病作用。在这项研究中,我们探索了 IgAN 大鼠的肠屏障特征。
我们将 17 只雄性 Sprague Dawley(SD)大鼠随机分为正常对照组(NC;n=9)和 IgAN 模型组(n=8)。取回肠末端粪便进行肠道微生物 16sDNA 测序。我们还取回肠末端一段分析肠道形态,并检测紧密连接蛋白 zonula occludens-1(ZO-1)和闭合蛋白(OCLN)以及粘蛋白 2(MUC2)的 mRNA 和蛋白表达。然后测量血清二胺氧化酶(DAO)和 D-乳酸(D-LA)水平,这是肠通透性的生物标志物。
与 NC 组相比,IgAN 模型组 ZO-1(t=4.216,P=0.0007)、OCLN(t=2.413,P=0.029)和 MUC2(t=0.859,P<0.0001)的 mRNA 表达水平明显降低。ZO-1(t=7.349,P<0.0001)和 OCLN(t=6.367,P<0.0001)的蛋白表达也在 IgAN 模型组中降低。相反,该组血清 DAO(t=3.758,P=0.0024)和 D-LA(t=2.246,P=0.0427)水平升高。在属水平上,IgAN 模型组中 Ruminococcus2 的相对丰度增加(P=0.0086)。
ZO-1、OCLN 和 MUC2 表达降低以及肠道微生物群失调与 IgAN 大鼠的肠屏障损伤有关。