Fig. 4.
Effects of APP on proliferation and viability of murine splenocytes treated and not treated with ConA. Cell proliferation and viability were measured by XTT metabolization (a) and BrdU incorporation (b). Murine splenocytes were cultured in vitro and activated using APP (0–80 μM) in the presence (○) or absence (•) of ConA (1 μg/ml) and for 72 h. Results are given as means ± SE; n=3