Figure 4
Figure 4. The number of cells with HSC cell surface markers is not restored after 15 months without MOZ. (A) Experimental design. Mice were treated with poly(I:C) and then left undisturbed for 15 months; bone marrow stem cell populations and stage of the cell cycle were then quantitated in 3 Mozfl/fl;Mx1-cre and 3 control Mozfl/fl mice. (B) Flow cytometry plots showing analyses of the LSK-CD34–FLT3– and the LSK-CD48–CD150+ populations in Mozfl/fl and Mozfl/fl;Mx1-cre bone marrow 15 months after poly(I:C) treatment. Note that these are similar to those shown in Figure 2. (C-D) Quantification of stem cell markers by flow cytometry of Mozfl/fl and Mozfl/fl;Mx1-cre bone marrow cells. Note the reduction in typical LSK-CD34–FLT3– and LSK-CD48–CD150+ populations. (E) Cell cycle analysis of stem/progenitor populations. Note the reduction in the number of cells in G0. Data are presented as the mean ± SEM.

The number of cells with HSC cell surface markers is not restored after 15 months without MOZ. (A) Experimental design. Mice were treated with poly(I:C) and then left undisturbed for 15 months; bone marrow stem cell populations and stage of the cell cycle were then quantitated in 3 Mozfl/fl;Mx1-cre and 3 control Mozfl/fl mice. (B) Flow cytometry plots showing analyses of the LSK-CD34FLT3 and the LSK-CD48CD150+ populations in Mozfl/fl and Mozfl/fl;Mx1-cre bone marrow 15 months after poly(I:C) treatment. Note that these are similar to those shown in Figure 2. (C-D) Quantification of stem cell markers by flow cytometry of Mozfl/fl and Mozfl/fl;Mx1-cre bone marrow cells. Note the reduction in typical LSK-CD34FLT3 and LSK-CD48CD150+ populations. (E) Cell cycle analysis of stem/progenitor populations. Note the reduction in the number of cells in G0. Data are presented as the mean ± SEM.

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