Figure 5
Figure 5. VLPs, HIV-1 and exosomes enter mDCs through a mechanism resistant to proteolysis. mDC capture of (A) VLPHIV-Gag-eGFP, (B) HIVNL43, or (C) ExosomesDiI. Pronase-treated or -untreated mDCs were pulsed for 15 minutes at 37°C with pronase or mock-treated VLPHIV-Gag-eGFP, HIVNL43, and ExosomesDiI. Protease pretreatments of either the cells or the particles were insufficient to prevent the capture of VLPHIV-Gag-eGFP, ExosomesDiI or HIVNL43 by mDCs. (C-E) Mean values and SEM from 6 independent experiments, including cells from at least 4 different donors.

VLPs, HIV-1 and exosomes enter mDCs through a mechanism resistant to proteolysis. mDC capture of (A) VLPHIV-Gag-eGFP, (B) HIVNL43, or (C) ExosomesDiI. Pronase-treated or -untreated mDCs were pulsed for 15 minutes at 37°C with pronase or mock-treated VLPHIV-Gag-eGFP, HIVNL43, and ExosomesDiI. Protease pretreatments of either the cells or the particles were insufficient to prevent the capture of VLPHIV-Gag-eGFP, ExosomesDiI or HIVNL43 by mDCs. (C-E) Mean values and SEM from 6 independent experiments, including cells from at least 4 different donors.

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