Figure 7.
Figure 7. Apoptotic cells in wt and Faslpr mice. (A) Flow cytometry analysis for the presence of apoptotic cells in the spleens and MLNs of wt and Faslpr mice by FITC-VAD-FMK staining is shown. Representative histograms for wt and Faslpr spleen cells are shown (top). Each histogram is gated on lymphocytes and the percent VAD-FMK+ is provided. The graph below shows the average ± SEM of percent apoptotic lymphocytes in the spleen and MLN of mice at 2 months and 3 months of age (n = 3). **A significant difference with wt (P < .01). (B) TUNEL-positive cell distributions in spleen and MLN of both wt and Faslpr mice. Both low (× 10) and high (× 40) magnifications are shown. Boxes indicate the areas of higher magnification. WP indicates white pulp; RP, red pulp; GC, germinal center; and F, follicle. (C) Macrophages from wt, Faslpr, MRL/Faslpr, and Merkd mice were incubated with apoptotic thymocytes for 60 minutes, and the percent of phagocytized thymocytes was determined by fluorescent microscopy. Controls are the percentage of live thymocytes (nonapoptotic) phagocytized. The graph is representative of 4 experiments and shows the average ± SEM of 3 mice per strain at both 2 months and 3 months of age. *P < .05, compared with wt.

Apoptotic cells in wt and Faslpr mice. (A) Flow cytometry analysis for the presence of apoptotic cells in the spleens and MLNs of wt and Faslpr mice by FITC-VAD-FMK staining is shown. Representative histograms for wt and Faslpr spleen cells are shown (top). Each histogram is gated on lymphocytes and the percent VAD-FMK+ is provided. The graph below shows the average ± SEM of percent apoptotic lymphocytes in the spleen and MLN of mice at 2 months and 3 months of age (n = 3). **A significant difference with wt (P < .01). (B) TUNEL-positive cell distributions in spleen and MLN of both wt and Faslpr mice. Both low (× 10) and high (× 40) magnifications are shown. Boxes indicate the areas of higher magnification. WP indicates white pulp; RP, red pulp; GC, germinal center; and F, follicle. (C) Macrophages from wt, Faslpr, MRL/Faslpr, and Merkd mice were incubated with apoptotic thymocytes for 60 minutes, and the percent of phagocytized thymocytes was determined by fluorescent microscopy. Controls are the percentage of live thymocytes (nonapoptotic) phagocytized. The graph is representative of 4 experiments and shows the average ± SEM of 3 mice per strain at both 2 months and 3 months of age. *P < .05, compared with wt.

Close Modal

or Create an Account

Close Modal
Close Modal