Figure 1
Figure 1. Single-cell analysis of MAPK activation in ex vivo human CD4+CD25+ Treg cells and CD4+CD25− T cells following TCR activation. (A) Ex vivo CD4+ T cells were left unstimulated or stimulated with crosslinked αCD3/CD28 mAbs for 10 minutes and stained for CD4, CD25, and phospho-ERK1/2. Histograms depicting levels of phospho-ERK were generated by gating on subsets of CD4+CD25high or CD4+CD25− T cells. (B) Geometric mean fluorescence intensities (MFIs) of cell populations stained with anti–phospho-ERK1/2 or (C) anti–phospho-p38 Abs were determined over a 60-minute time course following activation with αCD3/CD28 mAbs. The experiment was performed 3 times with similar results, and a representative analysis is shown. The inset is the fold change in MFI from resting to activation (at 10 minutes), with each point representing a separate experiment and horizontal bars representing the mean.

Single-cell analysis of MAPK activation in ex vivo human CD4+CD25+ Treg cells and CD4+CD25 T cells following TCR activation. (A) Ex vivo CD4+ T cells were left unstimulated or stimulated with crosslinked αCD3/CD28 mAbs for 10 minutes and stained for CD4, CD25, and phospho-ERK1/2. Histograms depicting levels of phospho-ERK were generated by gating on subsets of CD4+CD25high or CD4+CD25 T cells. (B) Geometric mean fluorescence intensities (MFIs) of cell populations stained with anti–phospho-ERK1/2 or (C) anti–phospho-p38 Abs were determined over a 60-minute time course following activation with αCD3/CD28 mAbs. The experiment was performed 3 times with similar results, and a representative analysis is shown. The inset is the fold change in MFI from resting to activation (at 10 minutes), with each point representing a separate experiment and horizontal bars representing the mean.

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