Figure 2.
Trametinib suppresses phosphorylation of ERK1/2 in T and B cells. (A) PBMCs were isolated from patients and stimulated with PMA and ionomycin for 15 minutes. Expression of phosphorylated ERK1/2 by CD4+ T, CD8+ T cells, and CD19+ B cells was analyzed after treatment (or not) with trametinib and tacrolimus (10 nM, 100 nM, and 1 µM). The numbers represent the frequencies of phospho-ERK1/2 cells compared with controls. (B) Aggregated percentages of cells CD4+/CD8+ T and CD19+ B cells showing phosphorylated ERK1/2 expression with PMA/Ionomycin stimulation for 4 hours (data expressed as means ± SEMs; n = 4 per group, gray; PMA and ionomycin stimulation, red; unstimulated). *P < .05; **P < .01; ***P < .001; ****P < .0001 (unpaired 2-tailed Student t test).

Trametinib suppresses phosphorylation of ERK1/2 in T and B cells. (A) PBMCs were isolated from patients and stimulated with PMA and ionomycin for 15 minutes. Expression of phosphorylated ERK1/2 by CD4+ T, CD8+ T cells, and CD19+ B cells was analyzed after treatment (or not) with trametinib and tacrolimus (10 nM, 100 nM, and 1 µM). The numbers represent the frequencies of phospho-ERK1/2 cells compared with controls. (B) Aggregated percentages of cells CD4+/CD8+ T and CD19+ B cells showing phosphorylated ERK1/2 expression with PMA/Ionomycin stimulation for 4 hours (data expressed as means ± SEMs; n = 4 per group, gray; PMA and ionomycin stimulation, red; unstimulated). *P < .05; **P < .01; ***P < .001; ****P < .0001 (unpaired 2-tailed Student t test).

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