Figure 7

rTB9.8 induces the nuclear translocation of IRF-1. RAW264.7 cells were cultured in the presence of rTB9.8 (5 µg/ml) for the indicated times, and cell lysates of total and nuclear proteins were prepared. Western blot analysis was used to examine the nuclear translocation of IRF-1. The cells were also stimulated with IFN-γ (10 U/ml), a known potent inducer of IRF-1 expression, as a positive control. Bottom, reprobing with anti-TBP and anti-β-actin to ensure equal loading. No IRF-1 protein was detectable in unstimulated cells at any of the time points examined. The data shown represent one of three independent experiments. The full-length blots are presented in Supplementary Figure 1.