Nanoparticle tracking analysis of extracellular vesicles reveals two populations of exosomes
A. V. Selenina, VA Kulichkova, А. Н. Томилин, А. С. Цимоха
Abstract
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A. V. Selenina, VA Kulichkova, А. Н. Томилин, А. С. Цимоха
Abstract
Open-access reader
Exosomes are extracellular vesicles of 30 to100 nm in diameter, which are secreted by various cells of mammals. It is known that exosomes represent a specific way of cell-to-cell communication. Mechanisms of secretion and uptake of these vesicles are not clear. To address this problem, we fused the transmembrane protein CD63, a known exosomal marker, at its N-termini to the EGFP protein. We have shown that these proteins exit cells as a part of exosomes, substantiated by the fluorescent nanoparticle tracking analysis. The analysis has also shown that there are two prevailing exosome populations in general population of vesicles.
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Exosomes are extracellular vesicles of 30 to100 nm in diameter, which are secreted by various cells of mammals. It is known that exosomes represent a specific way of cell-to-cell communication. Mechanisms of secretion and uptake of these vesicles are not clear. To address this problem, we fused the transmembrane protein CD63, a known exosomal marker, at its N-termini to the EGFP protein. We have shown that these proteins exit cells as a part of exosomes, substantiated by the fluorescent nanoparticle tracking analysis. The analysis has also shown that there are two prevailing exosome populations in general population of vesicles.
Key concepts: Microvesicles, Nanoparticle tracking analysis, Exosome, CD63, Vesicle, Secretion, Cell biology, Population