NKA function following D2L DAR transfection. HEK293T
cells were transfected with 7.5 μg of either D2L cDNA or empty
pcDNA vector (UTs). Cells were washed 24 h later, and for cells
involving pertussis toxin treatment (PTX), 125 ng/ml PTX was added to
media 16 h prior to experimentation. 48 h post-transfection, cells were
removed into assay buffer and 86Rb+ uptake, in the
presence or absence of dopamine (DA), was measured as described under
“Experimental Procedures.” Data were normalized for individual
experiments as a percentage of the Emax value for
UT cells alone and are expressed as mean ± S.E. of five
independent experiments, each conducted in duplicate. All statistical analyses
were performed using one-way ANOVA with Bonferroni's post-test; *,
p < 0.05; **, p < 0.01. UT raw
Emax values ranged from 109 to 219 pmol/mg
protein/min.