Figure 5.
Immuno-characterization of M(0) THP-1 macrophage-like treated with sEVsPBDE+LPS Macrophage sEVsPBDE+LPS on resting M(0) THP-1 macrophage-like affecting expression of surface markers of macrophage polarization by flow cytometry analysis. (A) gating strategy analyzing the selected macrophage population for CD14/CD11b expression in each experimental condition. (B) Cumulative analysis of resting M(0) THP-1 macrophage-like treated with macrophage sEVsPBDE+LPS, or sEVsPBDE+LPS, indicated percentage of the CD14/CD11b cells expressing CCR7, CD80 and HLA-DR. Untreated cells (NT) and LPS were considered as experimental control condition. (C) Cumulative analysis of the Mean Fluorescence Intensity (MFI) of resting M(0) THP-1 macrophage-like treated with macrophage sEVsPBDE+LPS expressing CCR7, CD80 and HLA-DR. (D) Cumulative analysis of resting M(0) THP-1 macrophage-like treated with macrophage sEVsPBDE+LPS, or only DMSO, indicated percentage of the CD14/CD11b cells expressing CD38 and CD209. Untreated cells (NT) and LPS were considered as experimental control condition. Non statistical significance is indicated as ns. *P ≤ 0.05 by nonparametric Mann-Whitney test, unpaired and one-tailed with confidential interval 95%.
