Figure 4
Figure 4. Absence of chronic GCs in the gut-associated lymphoid tissues of Dicer1fl/flAicdaCre/+ mice. Flow cytometric analysis of GC B cells in the Peyer patches (PP; A), or mesenteric lymph nodes (mLN; B), of unchallenged Dicer1+/+AicdaCre/+ and Dicer1fl/flAicdaCre/+ mice. GC B cells were stained as described in Figure 3A. Numbers adjacent to outlined area indicated percentage of cells in the individual gate. (C) Confocal microscopy of PP cryosections from unchallenged Dicer1+/+AicdaCre/+ and Dicer1fl/flAicdaCre/+ mice. The sections were stained with the same cocktail of antibodies as described in Figure 3B to visualize B-cell follicles, FDCs, and GC B cells. Data are representative of more than 6 experiments (A-B) or 3 experiments (C).

Absence of chronic GCs in the gut-associated lymphoid tissues of Dicer1fl/flAicdaCre/+ mice. Flow cytometric analysis of GC B cells in the Peyer patches (PP; A), or mesenteric lymph nodes (mLN; B), of unchallenged Dicer1+/+AicdaCre/+ and Dicer1fl/flAicdaCre/+ mice. GC B cells were stained as described in Figure 3A. Numbers adjacent to outlined area indicated percentage of cells in the individual gate. (C) Confocal microscopy of PP cryosections from unchallenged Dicer1+/+AicdaCre/+ and Dicer1fl/flAicdaCre/+ mice. The sections were stained with the same cocktail of antibodies as described in Figure 3B to visualize B-cell follicles, FDCs, and GC B cells. Data are representative of more than 6 experiments (A-B) or 3 experiments (C).

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