2018
DOI: 10.1039/c7nr08800k
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Visualization and intracellular dynamic tracking of exosomes and exosomal miRNAs using single molecule localization microscopy

Abstract: Exosomes are small membrane vesicles secreted by a wide variety of cells. Studies have demonstrated that exosomal miRNAs can influence the biological processes of recipient cells. Therefore, direct imaging and tracking of exosomal miRNAs in living recipient cells are essential for exosome functional analysis. However, the moderate spatial resolution of conventional fluorescence microscopy limits the precise imaging and tracking of exosomes considering their relatively small size (<100 nm). Here, we took advant… Show more

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Cited by 55 publications
(57 citation statements)
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“…Exosomes Isolation : Isolation of exosomes from cell culture media was carried out as previously described, according to the manufacturer's instructions . For clinical sample detection, seven healthy samples (three were females and four males), seven breast cancer samples (all females), seven pancreatic cancer samples (two were females and five males) and seven unknown samples were enrolled in the study.…”
Section: Methodsmentioning
confidence: 99%
“…Exosomes Isolation : Isolation of exosomes from cell culture media was carried out as previously described, according to the manufacturer's instructions . For clinical sample detection, seven healthy samples (three were females and four males), seven breast cancer samples (all females), seven pancreatic cancer samples (two were females and five males) and seven unknown samples were enrolled in the study.…”
Section: Methodsmentioning
confidence: 99%
“…We and other have investigated cell uptake in several cell lines [ 150 , 151 , 152 , 153 ]. Several methods were used to study exosomal uptake in vitro and in vivo.…”
Section: Exosome Internalizationmentioning
confidence: 99%
“…New techniques, including nanoparticle tracking analysis (NTA) (11,12), tunable resistive pulse sensing (13,14), flow cytometry (FC) (15,16), and surface plasmon resonance (SPR) (17,18) are powerful, but have their own limitations in throughput, sensitivity, or multiplexing capability (8,9). Fundamental knowledge about how exosomes interact with cells to alter the physiology is difficult to discover, since conventional optical microscopy is not able to visualize exosomes, and complex labeling is required (19,20).…”
mentioning
confidence: 99%