2011
DOI: 10.1016/j.colsurfb.2011.05.013
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Characterisation of exosomes derived from human cells by nanoparticle tracking analysis and scanning electron microscopy

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Cited by 713 publications
(607 citation statements)
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“…To investigate this, we initially qualified the nanoparticle tracking analysis (NTA) as EV-quantification method and optimized a polyethylene glycol (PEG)-based large scale EV-preparation method (74,75). Testing PEG purified MSC-EVs in a mixed lymphocyte reaction assay we observed that in the presence of MSC-EVs less immune cells secreted proinflammatory cytokines than in their absence.…”
Section: Gvhdmentioning
confidence: 99%
“…To investigate this, we initially qualified the nanoparticle tracking analysis (NTA) as EV-quantification method and optimized a polyethylene glycol (PEG)-based large scale EV-preparation method (74,75). Testing PEG purified MSC-EVs in a mixed lymphocyte reaction assay we observed that in the presence of MSC-EVs less immune cells secreted proinflammatory cytokines than in their absence.…”
Section: Gvhdmentioning
confidence: 99%
“…Alix, TSG101) and in tetraspanins such as CD9, CD63, and CD81. As exosomes are generally smaller than the resolution limit of conventional optical techniques (light microscopy, flow cytometry scatter) (Van Der Pol et al 2010), highly dedicated technology is required for their detection, including electron microscopy, nanoparticle tracking analysis (NTA) (Sokolova et al 2011), tunable resistive pulse sensing (TRPS) (Maas, De Vrij, and Broekman 2014), and fluorescence-triggered high-resolution flow cytometry (Nolte- 'T Hoen et al 2012). Alternatively, exosomes may be characterized by bulk analysis techniques, such as Western blotting or bead-based flow cytome- try, a technique in which EV are linked to large beads and subsequently stained for exosome marker proteins (Suarez et al 2017;Volgers et al 2017).…”
Section: Exosomesmentioning
confidence: 99%
“…62 After separation, exosome identities are determined by at least two of these methods include atomic force microscopy (AFM), scanning electron microscopy (SEM), dynamic light scattering (DLS), flow cytometry (FCM), western blotting, nanoparticle tracking analysis (NTA), transmission electron microscopy (TEM) or ELISA. [63][64][65] After the isolation and characterization, exosomes for in vivo or in vitro applications must be frozen because they are unstable at room temperature and 37 °C. Exosomes can be stored for 6 months at -20 °C without cryopreservative agents.…”
Section: Isolation and Storage Of Exosomesmentioning
confidence: 99%