Fig. 1.
Fig. 1. Demonstration of specific antigenic peptide TCR-triggered CD25 upregulation on cytochromec peptide TCR transgenic mouse T lymphocytes. B10A TCR-transgenic mouse splenocytes were incubated at 5 × 106 cells/mL with 1 μmol/L of cytochrome c peptide for 2, 4, 6, and 8 hours. The cells were then labeled with (1) FITC antimouse CD25, (2) PE antimouse TCRαβ, and (3) PI. CD25 expression on the TCR+ cells was evaluated by flow cytometry by gating for PI− (live) and PE-antimouse TCRαβ+ cells. (A) Flow cytometry profiles of CD25-expressing TCRαβ+ cells. The shaded histograms show changes in CD25 expression after 2 (graph a), 4 (graph b), 6 (graph c), and 8 (graph d) hours of stimulation. The solid histogram (control) in graph a represents the CD25 level on T cells from a sample that was not incubated with antigenic peptide. (B) Time-dependent changes in percentages of CD25+ cells among TCRαβ+ cells was calculated from data in (A).

Demonstration of specific antigenic peptide TCR-triggered CD25 upregulation on cytochromec peptide TCR transgenic mouse T lymphocytes. B10A TCR-transgenic mouse splenocytes were incubated at 5 × 106 cells/mL with 1 μmol/L of cytochrome c peptide for 2, 4, 6, and 8 hours. The cells were then labeled with (1) FITC antimouse CD25, (2) PE antimouse TCRαβ, and (3) PI. CD25 expression on the TCR+ cells was evaluated by flow cytometry by gating for PI (live) and PE-antimouse TCRαβ+ cells. (A) Flow cytometry profiles of CD25-expressing TCRαβ+ cells. The shaded histograms show changes in CD25 expression after 2 (graph a), 4 (graph b), 6 (graph c), and 8 (graph d) hours of stimulation. The solid histogram (control) in graph a represents the CD25 level on T cells from a sample that was not incubated with antigenic peptide. (B) Time-dependent changes in percentages of CD25+ cells among TCRαβ+ cells was calculated from data in (A).

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