Figure 7
Batf3 silencing is not sufficient to impair DNGR-1+ BDCA3+ DC development in humanized mice. (A) CD11c+ HLA-DR+ live cells (same as in Figure 3) were analyzed for the expression of BDCA3 versus CD11b (top panel) among the GFP+ cells. Two populations were identified: gate I, BDCA3+, CD11b−; and gate II, BDCA3−, CD11b+. Numbers indicate percentage of cells in each of the indicated gates. (B) Frequency of BDCA3+ GFP+ (top panel) and of CD11b+ GFP+ cells (bottom panel) is shown. (C) Normalized expression of Batf3 within Lin− (CD3/14/16/19/20/56) HLA-DR+ GFP+ live cells, purified from the spleen of the humanized mice. (A,C) Data are representative of 2 independent experiments, with 4 mice for each sh-RNA. (B) Data are mean ± SEM of 2 independent experiments. *P < .05 (Mann-Whitney test). sh-CTRL indicates control; Sp, spleen; Lg, lung; and K, kidney.

Batf3 silencing is not sufficient to impair DNGR-1+ BDCA3+ DC development in humanized mice. (A) CD11c+ HLA-DR+ live cells (same as in Figure 3) were analyzed for the expression of BDCA3 versus CD11b (top panel) among the GFP+ cells. Two populations were identified: gate I, BDCA3+, CD11b; and gate II, BDCA3, CD11b+. Numbers indicate percentage of cells in each of the indicated gates. (B) Frequency of BDCA3+ GFP+ (top panel) and of CD11b+ GFP+ cells (bottom panel) is shown. (C) Normalized expression of Batf3 within Lin (CD3/14/16/19/20/56) HLA-DR+ GFP+ live cells, purified from the spleen of the humanized mice. (A,C) Data are representative of 2 independent experiments, with 4 mice for each sh-RNA. (B) Data are mean ± SEM of 2 independent experiments. *P < .05 (Mann-Whitney test). sh-CTRL indicates control; Sp, spleen; Lg, lung; and K, kidney.

Close Modal

or Create an Account

Close Modal
Close Modal