Light and electron microscopical analysis of nitric oxide synthase-like immunoreactive neurons in the rat retina

Citation
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
Citations number
64
Categorie Soggetti
da verificare
Journal title
VISUAL NEUROSCIENCE
ISSN journal
09525238 → ACNP
Volume
16
Issue
2
Year of publication
1999
Pages
379 - 389
Database
ISI
SICI code
0952-5238(199903/04)16:2<379:LAEMAO>2.0.ZU;2-H
Abstract
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.