EV preparations were characterized according to the guidelines of the International Society for Extracellular Vesicles [16 (link)] and as described previously by us [11 (link)]. EV size and concentration was measured by nanoparticle tracking analysis (NanoSight NS300, Malvern Instruments, UK). EV markers were evaluated by western blot and the shape of the EVs was evaluated by electron microscopy [11 (link)].
To isolate TdTomato-labeled EVs, we transduced breast cancer cells with a lentiviral vector to express palmitoylated TdTomato (PalmtdTomato) [53 (link)]. The DNA construct was a gift from Dr. X. Breakefield, Massachusetts General Hospital. The fluorescence label of the isolated EVs were evaluated by fluorescent microscopy and plate reader (SpectraMax M2 plate reader, Molecular Devices LLC, San Joses, CA, USA).