Figure 4
Figure 4. Cdc42 deletion promotes expansion of myeloid cells. (A) Representative FACS analysis of bone marrow cells by Gr1/Mac1 staining of the indicated genotypes at 14 DPI. P2 gating represents the Mac-1+, Gr-1lo population of immature monocytic cells. The numbers shown indicate the percentage of cells within each gate. (B) The frequencies of Gr1+/Mac1+ cells from bone marrow, peripheral blood, and spleens determined by flow cytometry are shown. (C) Mice were injected with one dose of BrdU 2 hours prior to being killed. Representative histograms (left) and statistical quantification (right) of BrdU incorporation determined by flow cytometry of the Gr1+/Mac1+ bone marrow cells and splenocytes are shown. (D) Representative FACS analysis of Gr1+/Mac1+ cells from WT and KO bone marrow by annexin V/7-AAD staining shows increased survival of the KO cells. Numbers indicate percentage of cells within each gate.

Cdc42 deletion promotes expansion of myeloid cells. (A) Representative FACS analysis of bone marrow cells by Gr1/Mac1 staining of the indicated genotypes at 14 DPI. P2 gating represents the Mac-1+, Gr-1lo population of immature monocytic cells. The numbers shown indicate the percentage of cells within each gate. (B) The frequencies of Gr1+/Mac1+ cells from bone marrow, peripheral blood, and spleens determined by flow cytometry are shown. (C) Mice were injected with one dose of BrdU 2 hours prior to being killed. Representative histograms (left) and statistical quantification (right) of BrdU incorporation determined by flow cytometry of the Gr1+/Mac1+ bone marrow cells and splenocytes are shown. (D) Representative FACS analysis of Gr1+/Mac1+ cells from WT and KO bone marrow by annexin V/7-AAD staining shows increased survival of the KO cells. Numbers indicate percentage of cells within each gate.

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