2018
DOI: 10.1007/s13238-018-0529-4
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Effect of pH, temperature and freezing-thawing on quantity changes and cellular uptake of exosomes

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Cited by 214 publications
(186 citation statements)
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“…[46] A subset of samples used for validation was used for isolating small EVs using ultracentrifugation sucrose density gradient method. [51,52] Small EVs including exosomes play important role in intercellular communication and execute its functions on different cell types. [47][48][49] We characterized average size of the isolated small EVs using DLS and Nanosight tracking analysis (NTA) could be useful for calculating both number and diameter information.…”
Section: Discussionmentioning
confidence: 99%
“…[46] A subset of samples used for validation was used for isolating small EVs using ultracentrifugation sucrose density gradient method. [51,52] Small EVs including exosomes play important role in intercellular communication and execute its functions on different cell types. [47][48][49] We characterized average size of the isolated small EVs using DLS and Nanosight tracking analysis (NTA) could be useful for calculating both number and diameter information.…”
Section: Discussionmentioning
confidence: 99%
“…EV isolations from the culture medium were performed with Platform period cultures. Chlamydomonas cells were cultured in normal TAP medium 42 and incubated at 25°C under continuous light, with a light intensity 180-200 μmol photons m -2 s -1 . The EV isolation experiments were performed at the logarithmic (sample "Log", 1.0 × 10 7 cells mL -1 ), nitrogen depletion (sample "N-", 1.5 × 10 7 cells mL -1 cells after culture for 3 days in the TAP-N culture medium, using NaCl instead of NH 4 Cl), nitrogen recovery (sample "NR", 1.5 × 10 7 cells mL -1 cells re-added N-cells with full TAP medium and cultured for another 3 days) and platform stages (sample "Pla", 2.5 × 10 7 cells mL -1 cells from Log continuous culture in TAP medium after 8 days).…”
Section: Methodsmentioning
confidence: 99%
“…On the other hand, storage at 37 °C leads to a reduction in exosome size. Currently, there are no standard criteria for the storage of exosomes …”
Section: Exosomesmentioning
confidence: 99%
“…The most common method for exosome isolation remains a sucrose‐based gradient ultracentrifugation (density of exosomes is usually in the range of 1.12–1.19 g per mL), but other methods based on precipitation (such as ExtraPEG described in a patent application) have been developed, yielding higher exosome concentrations but with the presence of some impurities in the form of co‐precipitated proteins . In the most recent study, the representative markers used to detect exosomes after isolation were ALIX (an ALG‐2‐interacting protein X), HSP70 (a heat shock protein 70) and TSG101 (a tumour susceptibility gene 101) . The intracellular protein impurities level can often be estimated by detecting β‐tubulin (exosomes do not possess any cytoskeleton‐like support).…”
Section: Exosomesmentioning
confidence: 99%
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