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. 2003 Apr 1;17(7):883–895. doi: 10.1101/gad.1063703

Figure 5.

Figure 5

Defective cell growth of tcasp8−/− T-cells. (A) [3H]Thymidine incorporation in tcasp8−/− and control purified T-cells after 48 or 72 h of stimulation with anti-CD3 (2 or 5 μg/mL) with or without costimulation by anti-CD28 (2 μg/mL) or IL-2 (100 U/mL). Representative experiments are shown. (B) [3H]Thymidine incorporation in tcasp8−/− and control purified T-cells after stimulation with PMA and ionomycin (concentrations in nanograms per milliliter). Representative experiments are shown. (C) [3H]Thymidine incorporation in B-cells purified from tcasp8−/− and control mice after 48 or 72 h of activation with various stimuli. (D) The proportion of T-cells in G0/G1, S, and G2/M phases were similar in control and tcasp8−/− backgrounds after anti-CD3 and anti-CD28 stimulation. The larger G1 subpopulation in the cycling tcasp8−/− T-cells at 48 and 72 h after stimulation indicates decreased survival of stimulated tcasp8−/− T-cells. G0/G1, S, and G2/M are calculated from the total number of cycling T-cells. Sub-G1 values represent the percentage of the total number of all cells cycling or dead.