Red blood cells as potential materials for microRNA biomarker study: overcoming heparin-related challenges.

IF 4.1 2区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Eftychia Kontidou, Rawan Humoud, Ekaterina Chernogubova, Michael Alvarsson, Lars Maegdefessel, Aida Collado, John Pernow, Zhichao Zhou
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引用次数: 0

Abstract

microRNAs (miRNAs) have been intensively studied as valuable biomarkers in cardiometabolic disease. Typically, miRNAs are detected in plasma or serum, but the use of samples collected in heparinized tubes is problematic for miRNA studies using quantitative PCR (qPCR). Heparin and its derivatives interfere with qPCR-based analysis, leading to a substantial reduction or even complete loss of detectable miRNA levels. Given that red blood cells (RBCs) express abundant miRNAs, whose expression is altered in cardiometabolic disease, RBCs could serve as an attractive alternative in biomarker studies. Here, we aim to explore the stability of miRNAs in RBCs collected from whole blood with different anticoagulants and thereby the potential of RBCs as alternative materials for miRNA biomarker studies. miRNA profiling was performed in human RBCs via RNA sequencing, followed by qPCR validation of selected miRNAs in RBCs and plasma in both heparinized and EDTA tubes. RNA sequencing revealed abundant miRNA presence in RBCs isolated from blood collected in EDTA tubes. miR-210-3p, miR-21-5p, miR-16-5p, and miR-451a were detected at comparable levels in RBCs isolated from both heparinized and EDTA tubes but not in plasma from heparinized tubes. Of note, miR-210-3p levels were consistently lower in RBCs from individuals with type 2 diabetes compared with healthy controls, regardless of anticoagulant type, supporting their potential as biomarker materials. In conclusion, RBCs offer a promising alternative for miRNA biomarker studies, overcoming heparin-related challenges.NEW & NOTEWORTHY microRNAs are valuable biomarkers in cardiometabolic disease, but heparinized tubes hinder their detection because of qPCR interference. RBCs, which express abundant microRNAs like miR-210-3p, may serve as an alternative. microRNAs, including miR-210-3p, are consistently detectable in RBCs at comparable levels between heparinized and EDTA tubes. miR-210-3p levels in RBCs are similarly reduced in heparinized tubes of patients with type 2 diabetes. Thus, RBCs offer a promising solution for miRNA biomarker studies, overcoming heparin-related challenges.

红细胞作为微 RNA 生物标记物研究的潜在材料:克服肝素相关挑战。
微小核糖核酸(miRNA)作为心脏代谢疾病的重要生物标志物已得到深入研究。通常,miRNA 是在血浆或血清中检测的,但使用肝素化试管采集的样本对于利用 qPCR 进行 miRNA 研究来说是个问题。肝素及其衍生物会干扰基于 qPCR 的分析,导致可检测到的 miRNA 水平大幅降低甚至完全丧失。鉴于红细胞(RBC)表达丰富的 miRNA,而这些 miRNA 的表达在心脏代谢疾病中会发生改变,因此红细胞可作为生物标志物研究中一种有吸引力的替代方法。在这里,我们旨在探索从使用不同抗凝剂的全血中采集的 RBC 中 miRNA 的稳定性,从而了解 RBC 作为 miRNA 生物标记物研究替代材料的潜力。通过 RNA 测序对人类 RBC 进行了 miRNA 分析,然后对肝素化管和 EDTA 管中 RBC 和血浆中选定的 miRNA 进行了 qPCR 验证。从肝素化试管和 EDTA 试管中分离出的红细胞中检测到的 miR-210-3p、miR-21-5p、miR-16-5p 和 miR-451a 水平相当,但在肝素化试管中分离出的血浆中检测不到。值得注意的是,与健康对照组相比,无论抗凝剂类型如何,2 型糖尿病患者的红细胞中 miR-210 的水平一直较低,这支持了它们作为生物标记物材料的潜力。总之,RBC 为 miRNA 生物标记物研究提供了一种有前途的替代方法,克服了肝素相关的难题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
9.60
自引率
10.40%
发文量
202
审稿时长
2-4 weeks
期刊介绍: The American Journal of Physiology-Heart and Circulatory Physiology publishes original investigations, reviews and perspectives on the physiology of the heart, vasculature, and lymphatics. These articles include experimental and theoretical studies of cardiovascular function at all levels of organization ranging from the intact and integrative animal and organ function to the cellular, subcellular, and molecular levels. The journal embraces new descriptions of these functions and their control systems, as well as their basis in biochemistry, biophysics, genetics, and cell biology. Preference is given to research that provides significant new mechanistic physiological insights that determine the performance of the normal and abnormal heart and circulation.
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