高原红细胞增多症患者血浆外泌体microRNA表达谱

IF 2.1 4区 医学 Q3 HEMATOLOGY
Shengyan Wang , Jie Ma , Huiping Qiu , Shizhen Liu , Shouli Zhang , Huihui Liu , Peili Zhang , Ri-li Ge , Guojie Li , Sen Cui
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引用次数: 0

摘要

高原红细胞增多症(HAPC)是一种以多种严重不良反应为特征的慢性高山病。其发病机制尚不清楚,迄今为止,尚未有研究调查藏族HAPC患者的血浆外显子组谱。在这项研究中,我们旨在通过测定microRNA (miRNA)特征来阐明HAPC的发病机制。我们使用下一代miRNA测序技术比较了8名HAPC患者和8名健康对照者的血浆外泌体miRNA表达谱。此外,我们使用透射电子显微镜、纳米颗粒跟踪分析和western blotting提取和鉴定血浆外泌体。我们使用定量逆转录聚合酶链反应(qRT-PCR)来验证血浆外泌体差异表达的mirna。最后,我们利用受试者工作特征(ROC)曲线分析了差异表达mirna对HAPC的诊断价值。我们从确认的血浆外泌体中检测到2007种mirna,包括1342种已知的mirna和665种新预测的mirna。我们通过qRT-PCR验证了前10个差异表达mirna的表达。HAPC患者hsa-miR-122-5p、hsa-miR-423-5p、hsa-miR-4433b-3p、hsa-miR-1291、hsa-miR-106b-5p表达水平显著上调,hsa-miR-200c-3p表达水平下调。本研究可为今后HAPC的研究提供背景知识,进一步促进这种常见病的新疗法的开发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Plasma exosomal microRNA expression profiles in patients with high-altitude polycythemia

High-altitude polycythemia (HAPC) is a chronic mountain sickness characterized by multiple severe ill-effects. Its pathogenesis is still unclear, and till date, no study has been conducted to investigate the plasma exome profile of Tibetan patients with HAPC. In this study, we aimed to elucidate the pathogenesis of HAPC by determining the microRNA (miRNA) signatures. We compared the plasma exosome miRNA expression profiles of eight patients with HAPC and eight healthy controls using next-generation miRNA sequencing. Further, we extracted and identified plasma exosomes using transmission electron microscopy, nanoparticle tracking analysis, and western blotting. We used quantitative reverse-transcription polymerase chain reaction (qRT-PCR) to validate differentially expressed plasma exosomal miRNAs. Finally, we analyzed the diagnostic values of the differentially expressed miRNAs for HAPC using receiver operating characteristic (ROC) curves. We detected 2007 miRNAs from confirmed plasma exosomes, including 1342 known miRNAs and 665 newly predicted miRNAs. We verified the expression of the top 10 differentially expressed miRNAs via qRT-PCR. Patients with HAPC showed significantly upregulated hsa-miR-122-5p, hsa-miR-423-5p, hsa-miR-4433b-3p, hsa-miR-1291, and hsa-miR-106b-5p expression levels, while hsa-miR-200c-3p expression was downregulated. This study may provide background knowledge for future studies on HAPC studies, which may further facilitate the development of novel therapies against this common disease.

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来源期刊
CiteScore
4.90
自引率
0.00%
发文量
42
审稿时长
14 days
期刊介绍: Blood Cells, Molecules & Diseases emphasizes not only blood cells, but also covers the molecular basis of hematologic disease and studies of the diseases themselves. This is an invaluable resource to all those interested in the study of hematology, cell biology, immunology, and human genetics.
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