Fig. 1: VHL expression in T cells is critical for the control of M. tuberculosis infection in mice.
From: HIF-1 stabilization in T cells hampers the control of Mycobacterium tuberculosis infection

a, b Vhl cKO and WT mice were infected via aerosol with 250 M. tuberculosis and sacrificed at indicated time points after infection. The log10 CFU in the lung (a) and spleen (b) of individual mice (n WT = 10, 9, 12; n Vhl cKO = 9, 9, 10 mice at 4, 6 and 8 weeks post infection (w.p.i.) respectively) are represented. c The weight change with respect to the uninfected group mean (day 0) during infection with M. tuberculosis of Vhl cKO and WT mice (n = 11 per group) is depicted. d Representative micrographs from hematoxylin-eosin-stained paraffin lung sections from Vhl cKO and WT mice 8 w.p.i. with M. tuberculosis (bar: 400 μm). e The cumulative mortality of Vhl cKO and WT mice (n = 9 per group) after M. tuberculosis infection is depicted. f The log10 CFU in the lungs and spleens of Hif1a cKO (n = 11) and WT (n = 9) mice 8 w.p.i. with M. tuberculosis are shown. g–i The representative dot plots of CD4 and CD8 (gated on T cells) in the lungs of Vhl cKO and WT mice before and 8 w.p.i. with M. tuberculosis (g), and the frequency of CD4 (h) and CD8 (i) T cells in the lungs (WT n = 4, 4, 6, 8 and Vhl cKO n = 4, 5, 6 and 8 mice at 0, 4, 6 and 8 w.p.i. respectively). j, k The frequency of CD4 and CD8 T cells in the lungs of Hif1a cKO and WT mice before (n = 4 per group) and 8 w.p.i. (n = 5 per group) are depicted. l, m The frequency of CD4 in spleens (l) and mediastinal lymph nodes (m) before and 8 w.p.i. with M. tuberculosis are shown (Vhl cKO n = 4, 7 and WT n = 4, 4 mice at 0 and 8 w.p.i., respectively). Rag2−/− mice were administered i.v. with either 2.106 Vhl cKO or WT CD4 T cells (n = 6) or left untreated 3 days after M. tuberculosis infection. The log10 CFU in the lungs and spleens (n) (n = 8 animals per group) and number of CD4 T cells (o) in lungs (n = 6 mice per group) 4 w.p.i. Each symbol represents one mouse, and the data are presented as the mean ± s.e.m. The p-values were calculated using either a two-tailed unpaired t test with Welch’s correction for no homoscedasticity and FDR approach for multiple comparison (a, b, f, h–m, o), a one-way ANOVA with Welch’s correction (n), a 2-way ANOVA with Sidak’s multiple comparison test (c), or a χ2 test (e). Source data are provided as a Source Data file.