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. 2007 Sep;18(9):3635–3644. doi: 10.1091/mbc.E07-01-0053

Figure 7.

Figure 7.

Induction of PI3K signaling by eIF2α kinases requires eIF2α phosphorylation. (A) GyrB.PKR cells were left untransfected or transfected with siRNA for the luciferase reporter gene (Luc; negative control) or siRNA for eIF2α for 72 h followed by treatment with 100 ng/ml coumermycin for 6 h. (B) GyrB.PKR and GyrB.PKRT487D cells were left untreated or treated with coumermycin for the indicated times. (C) HT1080 cells were left untreated or pretreated with 20 μM LY294002 for 1 h before treatment with 75 μM Sal003 for the indicated times. (D) eIF2α S/S and eIF2α A/A MEFs were left untreated or treated with thapsigargin (TG; 1 μM) for indicated times. (A–D) Protein extracts (50 μg) were subjected to immunoblotting against the indicated proteins. The data represents one out of three reproducible experiments.