Extended Data Fig. 3: A Srebp2-dependent metabolic program controls SI TRM formation. | Nature

Extended Data Fig. 3: A Srebp2-dependent metabolic program controls SI TRM formation.

From: Metabolic programs of T cell tissue residency empower tumour immunity

Extended Data Fig. 3: A Srebp2-dependent metabolic program controls SI TRM formation.

a, Quantification of gene expression by qPCR of shRNAmir control (shCd19) or shSrebf2 shRNAmir P14 CD8+ T cells before adoptive transfer. b, Frequency of effector shRNAmir control (shCd19) or shSrebf2 shRNAmir P14 CD8+ T cell populations in the spleen 7 days after LCMV infection. c, Frequency of memory shRNAmir control (shCd19) or shSrebf2 shRNAmir P14 CD8+ T cell populations in the spleen 21 days after LCMV infection. d, CRISPR/Cas9-mediated indel efficiency of the Srebf2 sgRNA construct on sorted transduced P14 CD8+ T cells before adoptive transfer. e, Frequency of effector sgCd19 or sgSrebf2 P14 CD8+ T cell populations in the spleen 7 days after LCMV infection. f, Frequency of memory sgCd19 or sgSrebf2 P14 CD8+ T cell populations in the spleen 21 days after LCMV infection. g, Total cell quantification of CD44high CD8+ T cells (left) and Tet+ CD8+ T cells (right) in the blood of Scap WT or Scap KO at different time points after LCMV infection. h, Total cell quantification of Tet+ CD8+ T cells (upper) and CD44high CD8+ T cells (lower) in SI, kidney, and liver of Scap WT or Scap KO at different time points after LCMV infection. i, Ratio of congenically distinct P14 CD8+ T cells transduced with a constitutively active nuclear form of human Srebp268 (nSrebp2) or an empty vector (Empty) from indicated tissues 7 days after LCMV infection. j, Flow cytometry analysis of cholesterol content by Filipin stain (left), and LDLR expression in P14 CD8+ T cells transduced with a bicistronic construct encoding Thy1.1 alone or Thy1.1 and nSrebp2 (right). P14 CD8+ T cells from the kidney, liver, WAT, and SI were gated on the IV population (h and i). Data are mean +/− s.e.m. and representative of at least two independent experiments, with a total of n = 2 (a), n = 4 (b-e), n = 5 (f), n = 6 (WT) and n = 7 (Scap KO) (g and h), n = 4 (i and j) mice and n = 2 (d) cell replicates. Two-sided unpaired (a, d, g, and h) and paired (j) t-Test. *P < 0.05, **P < 0.01, ***P < 0.005. Two-sided one-sample t-Test (i) #P < 0.05, ##P < 0.01, ###P < 0.005. Two-way ANOVA (h) ##P < 0.01.

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