In situ single step detection of exosome microRNA using molecular beacon

分子信标 微泡 外体 小RNA 生物标志物 链球菌溶血素 寡核苷酸 计算生物学 生物 基因 生物化学 细菌蛋白
作者
Ji Hye Lee,Jeong Ah Kim,Min Hee Kwon,Ji Yoon Kang,Won Jong Rhee
出处
期刊:Biomaterials [Elsevier]
卷期号:54: 116-125 被引量:133
标识
DOI:10.1016/j.biomaterials.2015.03.014
摘要

In situ single step detection of microRNAs (miRNA) in a whole exosome has been developed as a novel diagnosis method that can be utilized for various diseases. Exosomes are small extracellular vesicles that contain biomarker miRNAs produced from their originating cells and are known to travel through the circulatory system. This makes exosomal miRNAs from the body fluids an attractive biomarker that can lead to a paradigm shift in the diagnosis of disease. However, current techniques, including real-time PCR analysis, are time-consuming and laborious, making them unsuitable for exosomal miRNA detection for diagnosis. Thus, the development of alternative methods is necessary. Herein, we have demonstrated that exosomal miRNAs can be detected directly using a nano-sized fluorescent oligonucleotide probe, molecular beacon. MiRNA-21 in exosomes from breast cancer cells were detected successfully by molecular beacons in a quantitative manner. Permeabilization by streptolysin O treatment further enhanced the delivery of molecular beacons into exosomes, giving significantly increased signals from target miRNAs. In addition, we selectively detected cancer cell-derived exosomal miRNA-21 among heterogeneous exosome mixtures and in human serum. The method developed in the article is simple, fast, and sensitive, so it will offer great opportunities for the high-throughput diagnosis and prognosis of diseases.
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