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. Author manuscript; available in PMC: 2020 May 15.
Published in final edited form as: J Immunol. 2019 Apr 8;202(10):2873–2887. doi: 10.4049/jimmunol.1801577

Figure 3. In vitro polarized TH2 CD4+ T cells are more efficient at performing trogocytosis than TH1 and non-polarized cells.

Figure 3.

Non-polarized and in vitro polarized TH1 and TH2 T cell blasts were used in standard in vitro trogocytosis assay and expression of IL-4, GATA-3, IFNγ and T-bet in recovered T cells was assessed via flow cytometry. (A & B) 2D plots showing fluorescence intensity of (A) IL-4 vs. GATA-3, and (B) IFNγ vs. T-bet in polarized TH2 (grey) and TH1 (black), and non-polarized cells, 1 hour post recovery. Numbers in corners represent frequencies of cells in respective quadrants. (C & D) Histogram overlays showing the frequency of trogocytosed (C) MHCII I-Ek and (D) biotinylated APC membrane by polarized TH1 (grey line) TH2 (thick black line), and non-polarized cells (thin black line), with unstimulated controls in shaded grey for comparison. (E) Mean frequency of trog+ cells from non-polarized (left), TH1 (middle), and TH2 (right) CD4+ cells 1 hour post-recovery. Error bars represent ±SEM from three independent experiments, * = p≤ 0.05, *** = p≤ 0.001, and **** = p≤ 0.0001. All data shown is representative of three independent experiments.