Parikh Victoria N, Chan Stephen Y
Department of Internal Medicine, University of California San Francisco, San Francisco, CA, USA.
Methods Mol Biol. 2013;1024:157-72. doi: 10.1007/978-1-62703-453-1_12.
MicroRNAs (miRNAs) are small, noncoding RNA molecules that negatively regulate gene expression and control a wide range of cellular processes. Extracellular forms of miRNA circulating in the bloodstream (circulating miRNA, c-miRNA) are of increasing interest for their potential as biomarkers and long-range physiological signaling molecules. Precise measurement of intracellular miRNA expression is possible but can be challenging, especially in the context of specialized tissue niches in vivo. The accurate measurement of extracellular miRNA presents other obstacles stemming from their low concentrations and confounding sources of intracellular miRNA that contaminate RNA extraction protocols. Here, we describe multiple methods to isolate extracellular miRNA from cell culture media, serum, and plasma in order to accurately measure their variable expression under different conditions. We additionally describe an in situ staining protocol designed to not only quantify but also localize miRNA in formalin-fixed paraffin-embedded tissue that may prove useful in describing the action of c-miRNA before they leave their tissue of origin and after they potentially arrive at their target destination.
微小RNA(miRNA)是一类小的非编码RNA分子,它们通过负向调控基因表达来控制广泛的细胞过程。循环于血液中的细胞外形式的miRNA(循环miRNA,c-miRNA)作为生物标志物和远距离生理信号分子的潜力,正受到越来越多的关注。精确测量细胞内miRNA表达是可行的,但可能具有挑战性,尤其是在体内特殊组织微环境的背景下。细胞外miRNA的准确测量还存在其他障碍,这源于它们的低浓度以及污染RNA提取方案的细胞内miRNA的混杂来源。在这里,我们描述了多种从细胞培养基、血清和血浆中分离细胞外miRNA的方法,以便准确测量它们在不同条件下的可变表达。我们还描述了一种原位染色方案,该方案不仅旨在定量,还能在福尔马林固定石蜡包埋组织中定位miRNA,这在描述c-miRNA在离开其起源组织之前以及可能到达其目标目的地之后的作用方面可能会很有用。