In the rabbit retina, the nuclear dye, 4,6,diamidino-2-phenylindole (D
API), selectively labels a third type of amacrine cell, in addition to
the previously characterized type a and type b cholinergic amacrine c
ells. In this study, these ''DAPI-3'' amacrine cells have been charact
erized with respect to their somatic distribution, dendritic morpholog
y, and neurotransmitter content by combining intracellular injection o
f biotinylated tracers with wholemount immunocytochemistry. There are
about 100,000 DAPI-3 amacrine cells in total, accounting for 2% of all
amacrine cells in the rabbit retina, and their cell density ranges fr
om about 130 cells/mm(2) in far-peripheral retina to 770 cells/mm(2) i
n the visual streak. The thin varicose dendrites of the DAPI-3 amacrin
e cells form a convoluted dendritic tree that is symmetrically bistrat
ified in S1/S2 and S4 of the inner plexiform layer. Tracer coupling sh
ows that the DAPI-3 amacrine cells have a fivefold dendritic-field ove
rlap in each sublamina, with the gaps in the arborization of each cell
being occupied by dendrites from neighboring cells. The DAPI-3 amacri
ne cells consistently show the strongest glycine immunoreactivity in t
he rabbit retina and they also accumulate exogenous [H-3]-glycine to a
high level. By contrast, the An amacrine cells, which are the best ch
aracterized glycinergic cells in the retina, are amongst the most weak
ly labelled of the glycine-immunopositive amacrine cells. The DAPI-3 a
macrine cells costratify narrowly with the cholinergic amacrine cells
and the On-Off direction-selective ganglion cells, suggesting that the
y may play an important role in movement detection.