Figure 1.
Figure 1. Normal thymocyte development in c-myc+/– mice. (A) Thymus cellularity (mean ± SD; n = 5) is shown for wt and c-myc+/– mice. *P < .05. (B) Thymocytes from wt and c-myc+/– littermates were analyzed for expression of TCRαβ, TCRγδ, CD4, and CD8. The numbers shown represent the percentage of cells within each quadrant. (C) Subpopulations of DN thymocytes in wt and c-myc+/– littermates were analyzed for expression of CD44 and CD25 gated on lin– cells (defined as negative for markers expressed by mature cells such as TCRαβ, TCRγδ, CD3, CD4, CD8, B220, NK1.1, CD11b, and Gr1). (D) Cell-cycle analysis of DN, DP, CD8SP, and CD4SP thymocytes from wt and c-myc+/– littermates was performed by Hoechst staining and FACS analysis. The numbers shown represent the mean percentage ± SD of cells in S-G2-M phases. The results shown are representative of 2 experiments and 5 mice per group (4 months old) were analyzed in each experiment.

Normal thymocyte development in c-myc+/– mice. (A) Thymus cellularity (mean ± SD; n = 5) is shown for wt and c-myc+/– mice. *P < .05. (B) Thymocytes from wt and c-myc+/– littermates were analyzed for expression of TCRαβ, TCRγδ, CD4, and CD8. The numbers shown represent the percentage of cells within each quadrant. (C) Subpopulations of DN thymocytes in wt and c-myc+/– littermates were analyzed for expression of CD44 and CD25 gated on lin cells (defined as negative for markers expressed by mature cells such as TCRαβ, TCRγδ, CD3, CD4, CD8, B220, NK1.1, CD11b, and Gr1). (D) Cell-cycle analysis of DN, DP, CD8SP, and CD4SP thymocytes from wt and c-myc+/– littermates was performed by Hoechst staining and FACS analysis. The numbers shown represent the mean percentage ± SD of cells in S-G2-M phases. The results shown are representative of 2 experiments and 5 mice per group (4 months old) were analyzed in each experiment.

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