In situ single step detection of exosome microRNA using molecular beacon

被引:135
作者
Lee, Ji Hye [1 ]
Kim, Jeong Ah [2 ]
Kwon, Min Hee [1 ]
Kang, Ji Yoon [3 ]
Rhee, Won Jong [1 ]
机构
[1] Incheon Natl Univ, Div Bioengn, Inchon 406772, South Korea
[2] MIT, Dept Mech Engn, Cambridge, MA 02139 USA
[3] Korea Inst Sci & Technol KIST, Brain Sci Inst, Ctr BioMicrosyst, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
Exosome; Molecular beacon; microRNA; Cancer; Diagnosis; MESSENGER-RNA; LIVING CELLS; MICROVESICLES; QUANTIFICATION; INHIBITION; BIOMARKERS; DELIVERY; TARGETS; MIRNAS; SERUM;
D O I
10.1016/j.biomaterials.2015.03.014
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
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 0 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. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:116 / 125
页数:10
相关论文
共 46 条
[1]   Tumor exosomes expressing Fas ligand mediate CD8+ T-cell apoptosis [J].
Abusamra, AJ ;
Zhong, ZH ;
Zheng, XF ;
Li, M ;
Ichim, TE ;
Chin, JL ;
Min, WP .
BLOOD CELLS MOLECULES AND DISEASES, 2005, 35 (02) :169-173
[2]   MicroRNAs as biomarkers in rheumatic diseases [J].
Alevizos, Ilias ;
Illei, Gabor G. .
NATURE REVIEWS RHEUMATOLOGY, 2010, 6 (07) :391-398
[3]   In vitro quantification of specific microRNA using molecular beacons [J].
Baker, Meredith B. ;
Bao, Gang ;
Searles, Charles D. .
NUCLEIC ACIDS RESEARCH, 2012, 40 (02) :e13
[4]   Fluorescent Probes for Live-Cell RNA Detection [J].
Bao, Gang ;
Rhee, Won Jong ;
Tsourkas, Andrew .
ANNUAL REVIEW OF BIOMEDICAL ENGINEERING, 2009, 11 :25-47
[5]   MicroRNAs as biomarkers of disease onset [J].
Ciesla, Maciej ;
Skrzypek, Klaudia ;
Kozakowska, Magdalena ;
Loboda, Agnieszka ;
Jozkowicz, Alicja ;
Dulak, Jozef .
ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2011, 401 (07) :2051-2061
[6]   Antennapedia and HIV transactivator of transcription (TAT) "protein transduction domains" promote endocytosis of high molecular weight cargo upon binding to cell surface glycosaminoglycans [J].
Console, S ;
Marty, C ;
García-Echeverría, C ;
Schwendener, R ;
Ballmer-Hofer, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (37) :35109-35114
[7]   MicroRNAs in body fluids-the mix of hormones and biomarkers [J].
Cortez, Maria Angelica ;
Bueso-Ramos, Carlos ;
Ferdin, Jana ;
Lopez-Berestein, Gabriel ;
Sood, Anil K. ;
Calin, George A. .
NATURE REVIEWS CLINICAL ONCOLOGY, 2011, 8 (08) :467-477
[8]   Oncomirs - microRNAs with a role in cancer [J].
Esquela-Kerscher, A ;
Slack, FJ .
NATURE REVIEWS CANCER, 2006, 6 (04) :259-269
[9]   Selecting optimal oligonucleotide composition for maximal antisense effect following streptolysin O-mediated delivery into human leukaemia cells [J].
Giles, RV ;
Spiller, DG ;
Grzybowski, J ;
Clark, RE ;
Tidd, DM .
NUCLEIC ACIDS RESEARCH, 1998, 26 (07) :1567-1575
[10]  
Hessvik Nina Pettersen, 2013, Frontiers in Genetics, V4, P36, DOI 10.3389/fgene.2013.00036