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. 2020 May 30;10(16):7131–7149. doi: 10.7150/thno.44564

Figure 3.

Figure 3

Intracellular trafficking of EV-coated multi-antigenic nanovaccines and ROS generation for enhancing proteasome activity. (A-B) Cell uptake by DC2.4 cells and BMDCs determined by flow cytometry at 1, 2 and 4 h post-incubation with EV-coated nanovaccines. (C) Photothermally triggered endosomal escape. Confocal images of BMDCs treated with EV-coated nanovaccines without (left) and with (right) laser irradiation. Endosomes were stained with LysoTracker™ Red. EVs were labelled with DiO (green). Scale bar: 10 µm. (D) Effect of EV-coated hybrid nanovaccines on ROS generation in BMDCs under laser irradiation using H2DCFDA as an ROS tracker that was quantified by flow cytometry. (E) Proteasome activity in BMDCs was analyzed by a fluorometric assay kit. Data are presented as the means ± SD (n = 3). **P < 0.01, ***P < 0.005, vs the indicated groups.