Fig. 4.
Fig. 4. Induction of the transactivation of endogenous RARs on an RAR-responsive element by TT or 9CTT in APL-derived NB4 (A) and non-APL U937 (B) cells. Cells were transfected with TK-βREx3-LUC reporter by an electroporation technique and treated with TT or 9CTT for 24 hours. Luciferase activities were adjusted for the efficiency of transfection by cotransfected β-galactosidase activities. ATRA and 9CTA at 1 × 10-6 mol/L induced the luciferase activity to 7.7 and 16.6 U, respectively, in NB4 cells and 24.8 and 54.8 U, respectively, in U937 cells. Values represent the means of three separate experiments.

Induction of the transactivation of endogenous RARs on an RAR-responsive element by TT or 9CTT in APL-derived NB4 (A) and non-APL U937 (B) cells. Cells were transfected with TK-βREx3-LUC reporter by an electroporation technique and treated with TT or 9CTT for 24 hours. Luciferase activities were adjusted for the efficiency of transfection by cotransfected β-galactosidase activities. ATRA and 9CTA at 1 × 10-6 mol/L induced the luciferase activity to 7.7 and 16.6 U, respectively, in NB4 cells and 24.8 and 54.8 U, respectively, in U937 cells. Values represent the means of three separate experiments.

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