Mh. Chun et al., Light and electron microscopical analysis of nitric oxide synthase-like immunoreactive neurons in the rat retina, VIS NEUROSC, 16(2), 1999, pp. 379-389
We have investigated the morphology of the NOS-like immunoreactive neurons
and their synaptic connectivity in the rat retina by immunocytochemistry us
ing antisera against nitric oxide synthase (NOS). In the present study, sev
eral types of amacrine cells were labeled with anti-NOS antisera. Type 1 ce
lls had large somata located in the inner nuclear layer (INL) with long and
sparsely branched processes ramifying mainly in stratum 3 of the inner ple
xiform layer (IPL). Somata of type 2 cells with smaller diameters were also
located in the INL. Their fine processes branched mostly in stratum 3 of t
he IPL. A third population showing NOS-like immunoreactivity was a class of
displaced amacrine cells in the ganglion cell layer (GCL). Their soma size
was similar to that of the type 1 cells; however, their processes stratifi
ed mainly in strata 4 and 5 of the IPL. Labeled neurons were evenly distrib
uted throughout the retina, and the mean densities were 57.0 +/- 9.7 cells/
mm(2) for the type 1 cells, 239.3 +/- 43.4 cells/mm2 for the type 2 cells a
nd 121.2 +/- 27.5 cells/mm2 cells for the displaced amacrine cells. The syn
aptic connectivity of NOS-like immunoreactive amacrine cells was identified
in the IPL by electron microscopy. NOS-labeled amacrine cell processes rec
eived synaptic input from other amacrine cell processes and bipolar cell ax
on terminals in all strata of the IPL. The most frequent postsynaptic targe
ts of NOS-immunoreactive amacrine cells were other amacrine cell processes.
Ganglion cell dendrites were also postsynaptic to NOS-like immunoreactive
neurons in both sublaminae of the IPL. Synaptic outputs onto bipolar cells
were observed in sublamina b of the IPL. In addition, a few synaptic contac
ts between labeled cell processes were observed. Our results suggest that N
OS immunoreactive cells may be modulated by other amacrine cells and ON con
e bipolar cells, and act preferentially on other amacrine cells.