The emergence and maturation of dopaminergic neurons during postnatal development of the rabbit retina have been followed using high affinity uptake, content, synthesis, storage, metabolism, and release of dopamine as transmitter-specific physiological probes. Autoradiographic and histochemical studies have shown that dopamine-containing neurons in the rabbit retina belong to a class of amacrine cells whose processes ramify mainly in the most distal region of the inner plexiform layer. These neurons contain high concentrations of dopamine, take up dopamine by a high affinity mechanism, and release the accumulated dopamine by a Ca2+ -dependent mechanism upon depolarization of the retina with high extracellular K'. In addition, the rabbit retina contains significant activities of tyrosine 3-hydroxylase (TH, EC 1.14.16.2) and monoamine oxidase (EC 1.4.3.4), the rate-limiting enzymes for the biosynthesis and degradation of dopamine, respectively. In the present study, we show that certain neurons in the newborn retina already possess a specific mechanism for dopamine uptake. The position, density, morphology, and ramification of these cells in the developing retina strongly suggest that they will become dopaminergic neurons in the adult retina. In addition, the ability of the newborn retina to release the accumulated dopamine upon Ca"+-dependent K+ stimulation is qualitatively similar to that of the adult retina. These putative dopaminergic neurons are, however, probably immature at birth because newborn retinas contain very low levels of TH activities and endogenous dopamine. The activities of retinal TH are extremely low between days 0 and 6 after birth, increasing slowly to 30% of the adult level by day 18. There is then a drastic rise in TH activity, reaching the adult level by day 25. The concentration of dopamine in the developing retinas follows closely the increase in TH activity, rising in the same biphasic pattern and reaching the adult level at about 25 days after birth.Taken together, our results indicate that, in the rabbit retina, the commitment for certain neurons to be dopaminergic is made prenatally. This is similar to our earlier findings that putative GABAergic and glycinergic neurons also are determined prenatally. for y-aminobutyric acid (GABA), glycine, and dopamine as neurotransmitters (Ames and Pollen, 1969;Brandon et al., 1980;Dowling and Ehinger, 1978;Graham, 1974;Kong et al., 1980;Lam, 1976;Lam et al., 1979). The neurons which use these substances as transmitters have been shown to contain high concentrations of these substances and their synthetic enzymes, to possess high affinity uptake mechanisms for these transmitters, and Vol. 1, No. 10, Oct. 1981 to release them in response to appropriate depolarizing stimuli. We have recently used these specific properties as physiological probes to follow the development of the GABAergic, glycinergic, and dopaminergic systems in identified neurons during differentiation and maturation of Xenopus and rabbit retinas. This is the third pap...