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. 2016 Nov 14;213(12):2759–2772. doi: 10.1084/jem.20160612

Figure 6.

Figure 6.

TMEM16F is required for control of chronic viral infection. (A–C) WT or TMEM16F-KO mice were i.v. infected with 4 × 106 pfu LCMV clone 13 for 80 d (A and B) or 150 d (C). (A) Absolute number of GP33-tetramer–positive CD8 T cells per 106 PBMCs was analyzed by flow cytometry at indicated time points after infection. n = 4 for WT; n = 3 for KO. (B and C) Virus loads in serum in B at indicated time points and in kidney at 138 d after infection in C were determined by focus assay. (B) n = 4 for WT n = 3 for KO; (C) n = 4. (D) WT or TMEM16F-deficient BM chimeric mice were i.v. infected with 4 × 106 pfu LCMV clone 13 and sacrificed at day 150 after infection. Virus loads in kidney and liver of BM chimeric mice were determined by focus assay. LOD, limit of detection. n = 4 for WT; n = 3 for KO. Results are displayed as mean ± SEM of two to three independent experiments. Student’s t test was used. *, P < 0.05; **, P < 0.01; ****, P < 0.0001.