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. 2018 Aug 28;14(8):e1007252. doi: 10.1371/journal.ppat.1007252

Fig 3. Role of different lymphocyte subsets in the formation of NIFs and in the control of viral replication in the lung.

Fig 3

Various mouse strains deficient for different cell populations were infected with 106 PFU MCMV-3D, i.e. Ighm-/-, Cd3e-/-, Rag2-/-, and Rag2-/-Il2rg-/- mice and analyzed at 8dpi. (A) Immunofluorescence of NIFs in different mouse strains stained as indicated with an antibody against CD45 (white) and a nuclear staining with DAPI (blue); infected cells expressing mCherry (red); Scale bar 50 μm. (B+C) Quantification of the number of infected cells counted (B) per NIF or (C) per whole lung slice. (B) Dots represent NIFs; Mann-Whitney test compared to WT data performed with mean values of individual animals. (C) Dots represent means of 4 lung slices analyzed per animal. (B+C) open circles (WT) are identical to that shown in Fig 1C and 1D and Fig 2B; median + interquartile range (red); Mann-Whitney test compared to WT data performed with mean values of individual animals; pooled data from 2–3 independent experiments.