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  • The morphological characterization of orientation-biased displaced large-field ganglion cells in the central part of goldfish retina.

The morphological characterization of orientation-biased displaced large-field ganglion cells in the central part of goldfish retina.

The Journal of comparative neurology (2017-09-19)
Hideo Hoshi, Fumi Sato
ABSTRACT

The vertebrate retina has about 30 subtypes of ganglion cells. Each ganglion cell receives synaptic inputs from specific types of bipolar and amacrine cells ramifying at the same depth of the inner plexiform layer (IPL), each of which is thought to process a specific aspect of visual information. Here, we identified one type of displaced ganglion cell in the goldfish retina which had a large and elongated dendritic field. As a population, all of these ganglion cells were oriented in the horizontal axis and perpendicular to the dorsal-ventral axis of the goldfish eye in the central part of retina. This ganglion cell has previously been classified as Type 1.2. However, the circuit elements which synapse with this ganglion cell are not yet characterized. We found that this displaced ganglion cell was directly tracer-coupled only with homologous ganglion cells at sites containing Cx35/36 puncta. We further illustrated that the processes of dopaminergic neurons often terminated next to intersections between processes of ganglion cells, close to where dopamine D1 receptors were localized. Finally, we showed that Mb1 ON bipolar cells had ribbon synapses in the axonal processes passing through the IPL and made ectopic synapses with this displaced ganglion cell that stratified into stratum 1 of the IPL. These results suggest that the displaced ganglion cell may synapse with both Mb1 cells using ectopic ribbon synapses and OFF cone bipolar cells with regular ribbon synapses in the IPL to function in both scotopic and photopic light conditions.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Anti-Connexin 35/36 Antibody, clone 8F6.2, clone 8F6.2, Chemicon®, from mouse
Sigma-Aldrich
Anti-Dopamine D1A Receptor Antibody, CT, cytoplasmic, Chemicon®, from rabbit
Sigma-Aldrich
PP1, ≥98% (HPLC)