Dopamine D3 receptors expressed by all mesencephalic dopamine neurons

A polyclonal antibody was generated using synthetic peptides designed in a specific sequence of the rat D-3 receptor (D3R). Using transfected cells expressing recombinant D3R, but not D-2 receptor, this antibody labeled 45-80 kDa species in Western blot analysis, immunoprecipitated a soluble fraction of [I-125] iodosulpride binding, and generated immunofluorescence, mainly in the cytoplasmic perinuclear region of the cells. In rat brain, the distribution of immunoreactivity matched that of D3R binding, revealed using [I-125] R(+) trans-7-hydroxy-2-[N-propyl-N-(3'-iodo-2'- propenyl) amino] tetralin ([I-125]7-trans-OH-PIPAT), with dense signals in the islands of Calleja and mammillary bodies, and moderate to low signals in the shell of nucleus accumbens (AccSh), frontoparietal cortex, substantia nigra (SN), ventral tegmental area (VTA) and lobules 9 and 10 of the cerebellum. Very low or no signals could be detected in other rat brain regions, including dorsal striatum, or in D3R-deficient mouse brain. Labeling of perikarya of AccSh and SN/VTA appeared with a characteristic punctuate distribution, mostly at the plasma membrane where it was not associated with synaptic boutons, as revealed by synaptophysin immunoreactivity. In SN/VTA, D3R-immunoreactivity was found on afferent terminals, arising from AccSh, in which destruction of intrinsic neurons by kainate infusions produced a loss of D3R binding in both AccSh and SN/VTA. D3R-immunoreactivity was also found in all tyrosine hydroxylase (TH) positive neurons observed in SN, VTA and A8 retrorubral fields, where it could represent D-3 autoreceptors controlling dopamine neuron activities, in agreement with the elevated dopamine extracellular levels in projection areas of these neurons found in D3R-deficient mice.