Figure 1.
Figure 1. Genetic disruption of Pak2 in HSPCs induces MDSC expansion in the spleen. CD45.1+ naive BoyJ mice were noncompetitively transplanted with CD45.2+Pak2flox/floxMx1Cre+ (Pak2-KO) or CD45.2+Pak2flox/floxMx1Cre− (WT) BM cells and treated with polyIC. (A) Gr1highLy6G+ cells that were isolated from spleens suppressed T-cell proliferation. (B) The numbers of phenotypic granulocytic (CD11b+Ly6G+Ly6Clow) and monocytic (CD11b+Ly6Glow/−Ly6Chi) MDSCs are shown per spleen. (C-D) WT (C) and Pak2-KO (D) splenic CD45.2+Gr1highLy6G+ cells were stained with Giemsa. Inserts show morphology of cells at a high magnification. All scale bars represent 20 mm. Representative data from at least 3 experiments with 3 to 9 mice per genotype are shown.

Genetic disruption of Pak2 in HSPCs induces MDSC expansion in the spleen. CD45.1+ naive BoyJ mice were noncompetitively transplanted with CD45.2+Pak2flox/floxMx1Cre+ (Pak2-KO) or CD45.2+Pak2flox/floxMx1Cre (WT) BM cells and treated with polyIC. (A) Gr1highLy6G+ cells that were isolated from spleens suppressed T-cell proliferation. (B) The numbers of phenotypic granulocytic (CD11b+Ly6G+Ly6Clow) and monocytic (CD11b+Ly6Glow/−Ly6Chi) MDSCs are shown per spleen. (C-D) WT (C) and Pak2-KO (D) splenic CD45.2+Gr1highLy6G+ cells were stained with Giemsa. Inserts show morphology of cells at a high magnification. All scale bars represent 20 mm. Representative data from at least 3 experiments with 3 to 9 mice per genotype are shown.

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