Intrinsic cAMP signaling capacity is not affected in PDE4DKO MEFs.
A, the basal intracellular cAMP concentration in wild type and
PDE4DKO MEFs in all experiments performed is reported. The horizontal
lines represent the average of at least 14 separate experiments. cAMP
levels in wild type and PDE4DKO cells are not significantly different
(p > 0.05; Student's t test). B, PDE4DKO and
matched wild type MEFs were pretreated for 5 min with 10 μm
rolipram. Cells were then stimulated with 10 μm ISO for the
indicated times, after which the incubations were terminated and cAMP
concentrations were determined by RIA. Treatment with rolipram elevates cAMP
accumulation in both wild type and PDE4DKO MEFs (compare panel B with
Fig. 4A). In the
presence of rolipram, the genetic inactivation of PDE4D has no effect on
ISO-induced cAMP accumulation compared with wild type controls (p
> 0.05, two-way ANOVA).