Fig. 5.
Fig. 5. Induction of differentiation of NB4 cells. (A) Expression of CD11b antigens on NB4 cells. NB4 cells were treated for 3 days with several concentrations (10−10 to 10−7mol/L) of either 1,25D3 or Ro-25 9716, and then analyzed by FACS. (□), 1,25D3; (⌾), Ro 25-9716. (B) Combination of ATRA plus either 1,25D3 or Ro 25-9716 on differentiation of NB4 cells. NB4 cells were treated with 1,25D3 alone (10−9 to 10−10 mol/L, □), Ro 25-9716 alone (10−9 to 10−10 mol/L, ⌾), the combination of either ATRA (10−7 mol/L) plus 1,25D3 (10−9 to 10−10 mol/L, X), or ATRA (10−7 mol/L) plus Ro 25-9716 (10−9 to 10−10 mol/L, □), and differentiation was determined by NBT reduction. Results represent the mean of three experiments with triplicate dishes.

Induction of differentiation of NB4 cells. (A) Expression of CD11b antigens on NB4 cells. NB4 cells were treated for 3 days with several concentrations (10−10 to 10−7mol/L) of either 1,25D3 or Ro-25 9716, and then analyzed by FACS. (□), 1,25D3; (⌾), Ro 25-9716. (B) Combination of ATRA plus either 1,25D3 or Ro 25-9716 on differentiation of NB4 cells. NB4 cells were treated with 1,25D3 alone (10−9 to 10−10 mol/L, □), Ro 25-9716 alone (10−9 to 10−10 mol/L, ⌾), the combination of either ATRA (10−7 mol/L) plus 1,25D3 (10−9 to 10−10 mol/L, X), or ATRA (10−7 mol/L) plus Ro 25-9716 (10−9 to 10−10 mol/L, □), and differentiation was determined by NBT reduction. Results represent the mean of three experiments with triplicate dishes.

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