Figure 4

The majority of CD11b+Ly6Clo cells that develop in the liver after IRE treatment are side-scatter high, and express high levels of F4/80 and intermediate levels of MHCII. (a) Representative flow cytometry density plots showing Ly6C expression versus side-scatter (SSC), F4/80, MHCII, and CD64 of CD11b+ monocytes/macrophages isolated from the IRE-treated liver lobe compared to parts of the liver not directly treated by IRE (control) from the same animal. Rectangular gates define Ly6Clo cells that are “high” for the given marker. (b) Quantification of CD11b+Ly6Clo cells that are SSC, F4/80, MHCII, or CD64 high, as defined by the gates in (a), in control and IRE-treated parts of the liver. Two-tailed unpaired t tests show ***p < 0.001 and ****p < 0.0001. Individual points represent data from separate animals (n = 4). Graph bars and error bars show mean ± SEM. (c) Representative flow cytometry density plots showing that the majority (70%) of CD11b+Ly6Clo cells in IRE-treated liver are SSChi, and that this subset is also F4/80hi and MHCIIint. The remainder of the CD11b+Ly6Clo cells that are SSClo (30%) express lower levels of F4/80 and very high levels of MHCII.