Fig. 4.
Fig. 4. The detection of cells undergoing apoptosis in the Lin− population. Mice were inoculated with 1 × 105 PFU of MCMV. On day 3 pi, the mice were killed in order to remove their bone marrow cells. Using flow cytometry, the signals of PI, which represent the DNA contents, were examined after the Lin− populations were gated. The G0/G1-peak was adjusted at channel 100 and subdiploid cells were designated as cells undergoing apoptosis. Before the experiments, it was confirmed that a coefficient variance in the PI-stained thymocytes was ca. 2%. The numbers in the figure represent the percentage of cells undergoing apoptosis in the Lin− cells. *Significant increase versus uninfected control (P < .01).

The detection of cells undergoing apoptosis in the Lin population. Mice were inoculated with 1 × 105 PFU of MCMV. On day 3 pi, the mice were killed in order to remove their bone marrow cells. Using flow cytometry, the signals of PI, which represent the DNA contents, were examined after the Lin populations were gated. The G0/G1-peak was adjusted at channel 100 and subdiploid cells were designated as cells undergoing apoptosis. Before the experiments, it was confirmed that a coefficient variance in the PI-stained thymocytes was ca. 2%. The numbers in the figure represent the percentage of cells undergoing apoptosis in the Lin cells. *Significant increase versus uninfected control (P < .01).

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