Fig. 2: GFI1-expressing CD8+ T cells exhibit a TM cell molecular program.
From: GFI1-driven transcriptional and epigenetic programs maintain CD8+ T cell stemness and persistence

a, Shared and unique DEGs (P < 0.05) in activated CD11a+CD44+GFI1hi CD8+ T cells isolated from the spleen of Gfi1tdTomato/+ mice at D7 post infection with LCMVc13 or LCMVArm and analyzed by RNA-seq. b, Volcano plot of DEGs in GFI1hi CD8+ T cells from LCMVc13-infected mice as in a. Blue and red indicate genes upregulated in activated GFI1lo and GFI1hi CD8+ T cells, respectively. Gray dots indicate P > 0.05. c, DEseq2-normalized expression of selected genes in GFI1hi and GFI1lo CD8+ T cells isolated from LCMVc13-infected mice as in a. d, Gene set enrichment analysis of GFI1hi and GFI1lo CD8+ T cells isolated from LCMVc13-infected mice as in a, using a memory CD8+ T cells gene signature26. NES, normalized enrichment score. e, Shared and unique DEGs (P < 0.05) in CD44+CD62L+GFI1hi and CD44+Ly108+GFI1hi CD8+ TM cells isolated from the spleen of Gfi1tdTomato/+ mice at D7 post infection with LCMVc13 and analyzed by RNA-seq. f,g, Representative flow cytometry plots (f) and quantification (g) of spleen donor CD45.2+CD8+ T cells at D7 post LCMVArm infection in congenic C57BL/6 mice transferred intravenously (i.v.) with splenic CD8+ T cells isolated at D21 post LCMVArm infection from CD45.2+ Gfi1tdTomato/+ mice and infected with LCMVArm 24 h later. Data pooled from two experiments (n = 7 mice per group). h, Total donor CD45.2+CD8+ T cells at D14 post LCMVc13 infection in the spleen of congenic C57BL/6 recipients infected with LCMVc13 7 days before transfer of infection-matched (D7) CD8+ T cells isolated from LCMVc13-infected CD45.2+ Gfi1tdTomato/+ mice. Data pooled from two experiments (n = 5 or 7 mice per group). P values were calculated using a Wald’s test (b, d and e) or a two-tailed Student’s t-test (g and h). Data in g and h show means; error bars, s.e.m.