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. 2021 Mar 3;12:638676. doi: 10.3389/fimmu.2021.638676

Figure 6.

Figure 6

Suppression of MSU-induced mitochondrial production of the ROS by DcR3.Fc and HBD.Fc in M-Mϕ and GM-Mϕ. M-Mϕ (A) and GM-Mϕ (B) treated with hIgG, DcR3.Fc, or HBD.Fc- (3 μg/ml of each) were stained with MitoSOX (2.5 μM, 30 min) and then stimulated with MSU (300 μg/ml) for 1.5 or 3 h. The MitoSOX fluorescence was detected through the PE-channel by flow cytometry, and the median fluorescence intensity (MFIs) were shown in each histogram. The data shown were mean ± SD of three independent experiments. The statistical significance was determined by one-way ANOVA. *p < 0.05 was obtained by comparing DcR3.Fc- or HBD.Fc-treated group to hIgG-group.