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Simultaneous visualization of the subfemtomolar expression of microRNA and microRNA target gene using HILO microscopy

机译:使用HILO显微镜同时可视化microRNA和microRNA靶基因的亚皮膜下表达

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摘要

The family of microRNAs (miRNAs) not only plays an important role in gene regulation but is also useful for the diagnosis of diseases. A reliable method with high sensitivity may allow researchers to detect slight fluctuations in ultra-trace amounts of miRNA. In this study, we propose a sensitive imaging method for the direct probing of miR-10b (miR-10b-3p, also called miR-10b*) and its target (HOXD10 mRNA) in fixed cells based on the specific recognition of molecular beacons combined with highly inclined and laminated optical sheet (HILO) fluorescence microscopy. The designed dye-quencher-labelled molecular beacons offer excellent efficiencies of fluorescence resonance energy transfer that allow us to detect miRNA and the target mRNA simultaneously in hepatocellular carcinoma cells using HILO fluorescence microscopy. Not only can the basal trace amount of miRNA be observed in each individual cell, but the obtained images also indicate that this method is useful for monitoring the fluctuations in ultra-trace amounts of miRNA when the cells are transfected with a miRNA precursor or a miRNA inhibitor (anti-miR). Furthermore, a reasonable causal relation between the miR-10b and HOXD10 expression levels was observed in miR-10b* precursor-transfected cells and miR-10b* inhibitor-transfected cells. The trends of the miRNA alterations obtained using HILO microscopy completely matched the RT-qPCR data and showed remarkable reproducibility (the coefficient of variation [CV] = 0.86%) and sensitivity (<1.0 fM). This proposed imaging method appears to be useful for the simultaneous visualisation of ultra-trace amounts of miRNA and target mRNA and excludes the procedures for RNA extraction and amplification. Therefore, the visualisation of miRNA and the target mRNA should facilitate the exploration of the functions of ultra-trace amounts of miRNA in fixed cells in biological studies and may serve as a powerful tool for diagnoses based on circulating cancer cells.
机译:microRNA(miRNA)家族不仅在基因调控中起着重要作用,而且对疾病的诊断也很有用。一种可靠的高灵敏度方法可以使研究人员检测超痕量miRNA的细微波动。在这项研究中,我们基于分子信标的特异性识别,提出了一种在固定细胞中直接探测miR-10b(miR-10b-3p,也称为miR-10b *)及其靶标(HOXD10 mRNA)的灵敏成像方法。与高度倾斜和层压的光学片(HILO)荧光显微镜相结合。设计的染料淬灭剂标记的分子信标具有出色的荧光共振能量转移效率,使我们能够使用HILO荧光显微镜同时检测肝癌细胞中的miRNA和靶mRNA。不仅可以在每个单个细胞中观察到基本痕量的miRNA,而且所获得的图像还表明,当用miRNA前体或miRNA转染细胞时,该方法可用于监测超痕量miRNA的波动。抑制剂(anti-miR)。此外,在miR-10b *前体转染的细胞和miR-10b *抑制剂转染的细胞中观察到miR-10b和HOXD10表达水平之间的合理因果关系。使用HILO显微镜获得的miRNA改变趋势完全符合RT-qPCR数据,并显示出显着的可重复性(变异系数[CV] = 0.86%)和灵敏度(<1.0 fM)。拟议的成像方法似乎对同时显示超痕量的miRNA和靶标mRNA有用,并且排除了RNA提取和扩增的步骤。因此,在生物学研究中,miRNA和靶标mRNA的可视化应有助于探索固定细胞中超痕量miRNA的功能,并可作为基于循环癌细胞进行诊断的有力工具。

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