Fig. 9.
Fig. 9. Rolipram blocks cAMP catabolism in both sensitive and resistant lymphoid populations. One million cells from the leukemic cells of two CLL patients (top; [▧], patient no. 1; [▪], patient no. 2), magnetic bead-purified CD19+ B cells (middle; [▧], resting; [▪], stimulated), or IL-2 supplemented WMC (bottom panel) were cultured with media, 10 μmol/L rolipram, 40 μmol/L forskolin, or both agents for 2, 6, or 24 hours, as indicated. cAMP content was determined by radioimmunoassay. In the case of the CD19+ cells, the cells were first cultured in media or Fab′2 anti-IgG/M for 30 minutes before treatment with rolipram or forskolin. Data are the mean of duplicate wells for each condition and are representative of two experiments with similar results.

Rolipram blocks cAMP catabolism in both sensitive and resistant lymphoid populations. One million cells from the leukemic cells of two CLL patients (top; [▧], patient no. 1; [▪], patient no. 2), magnetic bead-purified CD19+ B cells (middle; [▧], resting; [▪], stimulated), or IL-2 supplemented WMC (bottom panel) were cultured with media, 10 μmol/L rolipram, 40 μmol/L forskolin, or both agents for 2, 6, or 24 hours, as indicated. cAMP content was determined by radioimmunoassay. In the case of the CD19+ cells, the cells were first cultured in media or Fab′2 anti-IgG/M for 30 minutes before treatment with rolipram or forskolin. Data are the mean of duplicate wells for each condition and are representative of two experiments with similar results.

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