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贾第虫感染后功能性胃肠疾病患者肠道中的比较表达谱分析。

Comparative expression profiling in the intestine of patients with Giardia-induced postinfectious functional gastrointestinal disorders.

作者信息

Martínez Cristina, Lasitschka Felix, Thöni Cornelia, Wohlfarth Carolin, Braun Alexander, Granzow Martin, Röth Ralph, Dizdar Vernesa, Rappold Gudrun A, Hausken Trygve, Langeland Nina, Hanevik Kurt, Niesler Beate

机构信息

Department of Human Molecular Genetics, Institute of Human Genetics, Heidelberg University, Heidelberg, Germany.

Lleida Institute for Biomedical Research Dr. Pifarré Foundation (IRBLleida), Lleida, Spain.

出版信息

Neurogastroenterol Motil. 2020 Sep;32(9):e13868. doi: 10.1111/nmo.13868. Epub 2020 May 11.

DOI:10.1111/nmo.13868
PMID:32391639
Abstract

BACKGROUND

A Giardia outbreak in Bergen, Norway, caused postinfectious functional gastrointestinal disorders (PI-FGIDs). Despite the devastating effects of this outbreak, it presented a unique chance to investigate the implication on the dysregulation of genetic pathways in PI-FGID.

METHODS

We performed the first comparative expression profiling of miRNAs and their potential target genes in microdissected rectal biopsies from 20 Giardia-induced PI-FGID patients vs 18 healthy controls by nCounter analysis. Subsequently, candidates were validated on protein level by immunostaining.

KEY RESULTS

miRNA profiling on rectal biopsy samples from 5 diarrhea-predominant PI-IBS cases compared to 10 healthy controls revealed differential expression in the epithelial layer. The top five regulated miRNAs were implicated in GI disease, inflammatory response, and immunological disease. Subsequently, these miRNAs and 100 potential mRNA targets were examined in 20 PI-FGID cases and 18 healthy controls in both the mucosal epithelium and the lamina propria. Although deregulation of the selected miRNAs could not be verified in the larger sample set, mRNAs involved in barrier function were downregulated in the epithelium. Pro-inflammatory genes and genes implicated in epigenetic modifications were upregulated in the lamina propria. Immunostaining for selected candidates on 17 PI-FGID cases and 16 healthy controls revealed increased tryptase levels as well as a decreased and aberrant subcellular expression of occludin.

CONCLUSIONS AND INFERENCES

Genes relevant to immune and barrier function as well as stress response and epigenetic modulation are differentially expressed in PI-FGIDs and may contribute to disease manifestation.

摘要

背景

挪威卑尔根市的一次贾第虫暴发导致了感染后功能性胃肠疾病(PI-FGIDs)。尽管这次暴发产生了严重影响,但它为研究PI-FGID中基因通路失调的影响提供了一个独特的机会。

方法

我们通过nCounter分析,对20例贾第虫诱导的PI-FGID患者与18名健康对照者的显微切割直肠活检组织中的miRNA及其潜在靶基因进行了首次比较表达谱分析。随后,通过免疫染色在蛋白质水平上对候选基因进行了验证。

主要结果

与10名健康对照者相比,对5例以腹泻为主的PI-IBS病例的直肠活检样本进行miRNA谱分析,结果显示上皮层存在差异表达。上调程度最高的前五种miRNA与胃肠道疾病、炎症反应和免疫疾病有关。随后,在20例PI-FGID病例和18名健康对照者的黏膜上皮和固有层中对这些miRNA和100个潜在的mRNA靶标进行了检测。尽管在更大的样本集中未能证实所选miRNA的失调,但上皮中参与屏障功能的mRNA表达下调。固有层中促炎基因和与表观遗传修饰有关的基因表达上调。对17例PI-FGID病例和16名健康对照者的选定候选基因进行免疫染色,结果显示类胰蛋白酶水平升高,以及闭合蛋白的亚细胞表达减少和异常。

结论与推论

与免疫和屏障功能以及应激反应和表观遗传调节相关的基因在PI-FGIDs中存在差异表达,可能导致疾病表现。

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