Circulating Cell and Plasma microRNA Profiles Differ between Non-ST-Segment and ST-Segment-Elevation Myocardial Infarction.

Jeanine A Ward, Nada Esa, Rahul Pidikiti, Jane E Freedman, John F Keaney, Kahraman Tanriverdi, Olga Vitseva, Victor Ambros, Rosalind Lee, David D McManus
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引用次数: 69

Abstract

Background: Differences in plasma and whole blood expression microRNAs (miRNAs) in patients with an acute coronary syndrome (ACS) have been determined in both in vitro and in vivo studies. Although most circulating miRNAs are located in the cellular components of whole blood, little is known about the miRNA profiles of whole blood subcomponents, including plasma, platelets and leukocytes in patients with myocardial ischemia.

Methods: Thirteen patients with a ST-segment-elevation (STEMI) or non-ST-segment elevation (NSTEMI) myocardial infarction were identified in the University of Massachusetts Medical Center Emergency Department (ED) or cardiac catheterization laboratory between February and June of 2012. Whole blood was obtained from arterial blood samples at the time of cardiac catheterization and cell-specific miRNA profiling was performed. Expression of 343 miRNAs was quantified from whole blood, plasma, platelets, and peripheral blood mononuclear cells using a high-throughput, quantitative Real-Time polymerase-chain reaction system (qRT-PCR).

Results: MiRNAs associated with STEMI as compared to NSTEMI patients included miR-25-3p, miR-221-3p, and miR-374b-5p. MiRNA 30d-5p was associated with plasma, platelets, and leukocytes in both STEMI and NSTEMI patients; miRNAs 221-3p and 483-5p were correlated with plasma and platelets only in NSTEMI patients.

Conclusions: Cell-specific miRNA profiles differed between patients with STEMI and NSTEMI. The miRNA distribution is also unique amongst plasma, platelets, and leukocytes in patients with ischemic heart disease or ACS. Our findings suggest unique miRNA profiles among the circulating subcomponents in patients presenting with myocardial ischemia.

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非st段抬高心肌梗死和st段抬高心肌梗死循环细胞和血浆microRNA谱差异
背景:体外和体内研究已经确定了急性冠脉综合征(ACS)患者血浆和全血microRNAs (miRNAs)表达的差异。尽管大多数循环miRNA位于全血的细胞成分中,但对心肌缺血患者的全血亚成分,包括血浆、血小板和白细胞的miRNA谱知之甚少。方法:2012年2月至6月在马萨诸塞大学医学中心急诊科(ED)或心导管实验室确诊的st段抬高(STEMI)或非st段抬高(NSTEMI)型心肌梗死患者13例。在心导管插入时从动脉血液样本中获得全血,并进行细胞特异性miRNA谱分析。采用高通量、定量实时聚合酶链反应系统(qRT-PCR)对全血、血浆、血小板和外周血单个核细胞中343种mirna的表达进行定量。结果:与非STEMI患者相比,与STEMI相关的mirna包括miR-25-3p、miR-221-3p和miR-374b-5p。在STEMI和NSTEMI患者中,MiRNA 30d-5p与血浆、血小板和白细胞相关;miRNAs 221-3p和483-5p仅在NSTEMI患者中与血浆和血小板相关。结论:细胞特异性miRNA谱在STEMI和NSTEMI患者之间存在差异。在缺血性心脏病或ACS患者的血浆、血小板和白细胞中,miRNA分布也是独特的。我们的研究结果表明,心肌缺血患者的循环亚组分中存在独特的miRNA谱。
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