Department of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Children's Hospital of Philadelphia Research Institute, Philadelphia, Pennsylvania.
Department of Pediatrics, Perelman School of Medicine at the University of Pennsylvania, Children's Hospital of Philadelphia Research Institute, Philadelphia, Pennsylvania
Am J Physiol Gastrointest Liver Physiol. 2014 Oct 15;307(8):G803-12. doi: 10.1152/ajpgi.00121.2014. Epub 2014 Aug 21.
The incidence of eosinophilic esophagitis (EoE) has increased in the past several years, yet our understanding of its pathogenesis remains limited. To test the hypothesis that microRNAs (miRNAs) are altered in children with EoE, miRNAs were profiled in esophageal mucosa biopsies obtained from patients with active disease (n = 5) and healthy control subjects (n = 6). Fourteen miRNAs were significantly altered between groups; four of these miRNAs were decreased in EoE patients. A panel of five miRNAs (miR-203, miR-375, miR-21, miR-223, and miR-142-3p) were selected for validation in an independent set of samples from control (n = 22), active disease (n = 22), inactive disease (n = 22), and gastroesophageal reflux disease (n = 6) patients. Each panel miRNA was significantly altered among groups. miRNA changes in esophageal biopsies were not reflected in the circulating RNA pool, as no differences in panel miRNA levels were observed in sera collected from the four patient groups. In addition, in contrast to previous studies, no change in esophageal miRNA levels was detected following treatment that resolved esophageal eosinophilia. In an effort to identify the ramifications of reduced esophageal miR-203, miR-203 activity was inhibited in cultured epithelial cells via expression of a tough decoy miRNA inhibitor. Luciferase reporter assays demonstrated that miR-203 does not directly regulate human IL-15 through targeting of the IL-15 3'-untranslated region. From these experiments, it is concluded that miRNAs are perturbed in the esophageal mucosa, but not the serum, of pediatric EoE patients. Further investigation is required to decipher pathologically relevant consequences of miRNA perturbation in this context.
嗜酸细胞性食管炎 (EoE) 的发病率在过去几年中有所增加,但我们对其发病机制的理解仍然有限。为了验证 miRNA 在 EoE 患儿中发生改变的假说,我们对来自活动期疾病患儿 (n = 5) 和健康对照受试者 (n = 6) 的食管黏膜活检标本进行了 miRNA 谱分析。两组间有 14 个 miRNA 显著改变;其中 4 个 miRNA 在 EoE 患者中减少。选择一组五个 miRNA(miR-203、miR-375、miR-21、miR-223 和 miR-142-3p)用于验证来自对照(n = 22)、活动期疾病(n = 22)、非活动期疾病(n = 22)和胃食管反流病(n = 6)患者的独立样本。每组 miRNA 在组间均有显著改变。食管活检中的 miRNA 变化并未反映在循环 RNA 池中,因为在来自四个患者组的血清中未观察到 miRNA 水平的差异。此外,与先前的研究相反,在缓解食管嗜酸性粒细胞增多的治疗后,未检测到食管 miRNA 水平的变化。为了确定食管 miR-203 减少的后果,我们通过表达坚硬的诱饵 miRNA 抑制剂在培养的上皮细胞中抑制 miR-203 的活性。荧光素酶报告基因测定表明,miR-203 不通过靶向 IL-15 3'-非翻译区直接调节人 IL-15。从这些实验中可以得出结论,miRNA 在儿科 EoE 患者的食管黏膜中发生改变,但在血清中未发生改变。需要进一步研究来阐明这种情况下 miRNA 扰动的病理相关后果。