Fig. 5.
Fig. 5. As2O3 combined with AA induces apoptosis in su-DHL-4 cells. (A) Morphologic features of apoptosis. Cells were treated for 24 hours. 1, Without treatment; 2, As2O3 (1 μmol/L); 3, AA (62.5 μmol/L); 4, As2O3 (1 μmol/L) with AA (62.5 μmol/L). Apoptotic cells were determined with fluorescence staining as described in Materials and Methods. (B) DNA fragmentation. Cells were treated for 24 hours and total DNA was isolated and separated on agarose gel. DNA ladder was visualized with EB as described in Materials and Methods. Lane M, size markers, λ DNA HindIII digest and φx174 RF DNAHaeII digest; lane 1, control; lane 2, As2O3 (1 μmol/L); lane 3, AA (62.5 μmol/L); lane 4, As2O3 (1 μmol/L) + AA (62.5 μmol/L); lane 5, AA (125 μmol/L); lane 6, As2O3 (1 μmol/L) + AA (125 μmol/L). (C) Activation of CPP32 and effect on Bcl-2 by treatments as in B.

As2O3 combined with AA induces apoptosis in su-DHL-4 cells. (A) Morphologic features of apoptosis. Cells were treated for 24 hours. 1, Without treatment; 2, As2O3 (1 μmol/L); 3, AA (62.5 μmol/L); 4, As2O3 (1 μmol/L) with AA (62.5 μmol/L). Apoptotic cells were determined with fluorescence staining as described in Materials and Methods. (B) DNA fragmentation. Cells were treated for 24 hours and total DNA was isolated and separated on agarose gel. DNA ladder was visualized with EB as described in Materials and Methods. Lane M, size markers, λ DNA HindIII digest and φx174 RF DNAHaeII digest; lane 1, control; lane 2, As2O3 (1 μmol/L); lane 3, AA (62.5 μmol/L); lane 4, As2O3 (1 μmol/L) + AA (62.5 μmol/L); lane 5, AA (125 μmol/L); lane 6, As2O3 (1 μmol/L) + AA (125 μmol/L). (C) Activation of CPP32 and effect on Bcl-2 by treatments as in B.

Close Modal

or Create an Account

Close Modal
Close Modal