Fig. 6.
Fig. 6. Cell cycle analysis of primitive hematopoietic stem cells after stimulation. Lin−Sca-1+ BM cells from Mx–c-fos or control littermates were cultured with SCF, IL-3, and IL-6 in the presence (200 U/mL) or absence of IFN-/β. (A) After 24 hours, the cells were lysed and the nuclei were stained with propidium iodide. DNA content in the nuclei was determined by FACS. Percentage of PI-labeled nuclei in S/G2/M phase of the cell cycle is indicated. (B) After 36 hours, cells were pulsed with BrdU for 3 hours. Incorporated BrdU was detected by anti-BrdU monoclonal antibody and positive cells were counted. Results represent mean and SD of four dishes. The data presented are representative of three independent experiments.

Cell cycle analysis of primitive hematopoietic stem cells after stimulation. LinSca-1+ BM cells from Mx–c-fos or control littermates were cultured with SCF, IL-3, and IL-6 in the presence (200 U/mL) or absence of IFN-/β. (A) After 24 hours, the cells were lysed and the nuclei were stained with propidium iodide. DNA content in the nuclei was determined by FACS. Percentage of PI-labeled nuclei in S/G2/M phase of the cell cycle is indicated. (B) After 36 hours, cells were pulsed with BrdU for 3 hours. Incorporated BrdU was detected by anti-BrdU monoclonal antibody and positive cells were counted. Results represent mean and SD of four dishes. The data presented are representative of three independent experiments.

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