Figure 3
Figure 3. Oxidized ATP, but not KN-62, prevents microvesicle shedding. Immature DCs in standard saline solution were seeded on a glass coverslip at 37°C at a concentration of 105/mL and were preincubated for 2 hours with the covalent P2XR blocker oATP prior to stimulation with 100 μM BzATP or 3 mM ATP (A). Image acquisition and analysis were as in Figure 1. Blocking of P2X7R was also run by supplementing sucrose saline solution with 100 nM KN-62 (B, ▪) or by overnight incubation of DCs with 10 μg/mL of a monoclonal anti-P2X7R (C, ▪). The negative control was run in the presence of irrelevant mouse IgG (⊡). Bar = 10 μm. Data are averages ± SE of 3 experiments performed with cells from 3 different donors.

Oxidized ATP, but not KN-62, prevents microvesicle shedding. Immature DCs in standard saline solution were seeded on a glass coverslip at 37°C at a concentration of 105/mL and were preincubated for 2 hours with the covalent P2XR blocker oATP prior to stimulation with 100 μM BzATP or 3 mM ATP (A). Image acquisition and analysis were as in Figure 1. Blocking of P2X7R was also run by supplementing sucrose saline solution with 100 nM KN-62 (B, ▪) or by overnight incubation of DCs with 10 μg/mL of a monoclonal anti-P2X7R (C, ▪). The negative control was run in the presence of irrelevant mouse IgG (⊡). Bar = 10 μm. Data are averages ± SE of 3 experiments performed with cells from 3 different donors.

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