Fig. 1.
Fig. 1. PML binds to STAT3 and inhibits its activity. / NIH3T3 (A,F), 293T (B), HepG2 (C,E,G), and 32D (D) cells were transfected with an appropriate reporter gene (4 × APRE-Luc [A-D], 4 × ISRE-Luc [E], or 3 × β-Cas-Luc [F-G]) along with the indicated expression vectors. Also, 293T cells were transfected with pEF-BOS-G-CSF-R/gp130 and HepG2 cells with G-CSF-R. Relative luciferase activities induced by IL-6, G-CSF, EPO, IFNα, or 1*6-STAT5 were quantitated. The results are shown as the means ± standard deviations (SDs) of triplicate cultures. Similar results were obtained from at least 4 independent experiments. (H-I) 293T cells were transfected with pEF-BOS-G-CSF-R/gp130 and the indicated expression vectors. After G-CSF stimulation, total cell lysates were isolated and subjected to immunoprecipitation (IP) and immunoblotting (IB) with the indicated antibodies.

PML binds to STAT3 and inhibits its activity.

NIH3T3 (A,F), 293T (B), HepG2 (C,E,G), and 32D (D) cells were transfected with an appropriate reporter gene (4 × APRE-Luc [A-D], 4 × ISRE-Luc [E], or 3 × β-Cas-Luc [F-G]) along with the indicated expression vectors. Also, 293T cells were transfected with pEF-BOS-G-CSF-R/gp130 and HepG2 cells with G-CSF-R. Relative luciferase activities induced by IL-6, G-CSF, EPO, IFNα, or 1*6-STAT5 were quantitated. The results are shown as the means ± standard deviations (SDs) of triplicate cultures. Similar results were obtained from at least 4 independent experiments. (H-I) 293T cells were transfected with pEF-BOS-G-CSF-R/gp130 and the indicated expression vectors. After G-CSF stimulation, total cell lysates were isolated and subjected to immunoprecipitation (IP) and immunoblotting (IB) with the indicated antibodies.

Close Modal

or Create an Account

Close Modal
Close Modal