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登革出血热肝组织微小 RNA 和异构体的差异表达分析与谱分析。

Differential expression analysis and profiling of hepatic miRNA and isomiRNA in dengue hemorrhagic fever.

机构信息

Center for Technological Innovation, Instituto Evandro Chagas, Ananindeua, PA, Brazil.

Instituto de Ciências Biológicas, Universidade Federal do Pará, Belém, PA, Brazil.

出版信息

Sci Rep. 2021 Mar 10;11(1):5554. doi: 10.1038/s41598-020-72892-w.

Abstract

Dengue virus causes dengue hemorrhagic fever (DHF) and has been associated to fatal cases worldwide. The liver is one of the most important target tissues in severe cases, due to its intense viral replication and metabolic role. microRNAs role during infection is crucial to understand the regulatory mechanisms of DENV infection and can help in diagnostic and anti-viral therapies development. We sequenced the miRNome of six fatal cases and compared to five controls, to characterize the human microRNAs expression profile in the liver tissue during DHF. Eight microRNAs were differentially expressed, including miR-126-5p, a regulatory molecule of endothelial cells, miR-122-5p, a liver specific homeostasis regulator, and miR-146a-5p, an interferon-regulator. Enrichment analysis with predicted target genes of microRNAs revealed regulatory pathways of apoptosis, involving MAPK, RAS, CDK and FAS. Immune response pathways were related to NF- kB, CC and CX families, IL and TLR. This is the first description of the human microRNA and isomicroRNA profile in liver tissues from DHF cases. The results demonstrated the association of miR-126-5p, miR-122-5p and miR-146a-5p with DHF liver pathogenesis, involving endothelial repair and vascular permeability regulation, control of homeostasis and expression of inflammatory cytokines.

摘要

登革热病毒会引发登革出血热(DHF),并已在全球范围内与致命病例相关联。由于其强烈的病毒复制和代谢作用,肝脏是严重病例中最重要的靶组织之一。miRNA 在感染过程中的作用对于理解 DENV 感染的调控机制至关重要,并且有助于开发诊断和抗病毒疗法。我们对六例致命病例的 miRNome 进行了测序,并与五例对照进行了比较,以描述 DHF 期间肝脏组织中人类 microRNAs 的表达谱。有 8 个 microRNAs 表达差异,包括调节内皮细胞的 miR-126-5p、肝脏特异性稳态调节剂 miR-122-5p 和干扰素调节剂 miR-146a-5p。对 microRNAs 的预测靶基因进行富集分析,揭示了涉及 MAPK、RAS、CDK 和 FAS 的凋亡调控途径。与 NF-κB、CC 和 CX 家族、IL 和 TLR 相关的免疫反应途径。这是首次对 DHF 病例肝脏组织中的人类 microRNA 和 isomicroRNA 图谱进行描述。结果表明,miR-126-5p、miR-122-5p 和 miR-146a-5p 与 DHF 肝脏发病机制有关,涉及内皮修复和血管通透性调节、稳态控制和炎症细胞因子的表达。

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