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Light and electron microscopy of the ground squirrel retina: Functional considerations
Author(s) -
West Roger W.
Publication year - 1976
Publication title -
journal of comparative neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.855
H-Index - 209
eISSN - 1096-9861
pISSN - 0021-9967
DOI - 10.1002/cne.901680304
Subject(s) - inner plexiform layer , axon , amacrine cell , biology , retina , neuroscience , inner nuclear layer , axon terminal , outer plexiform layer , ribbon synapse , ganglion , microbiology and biotechnology , synaptic vesicle , biochemistry , vesicle , membrane
Abstract Light and electron microscopy of Golgi‐impregnated ground squirrel retinas have revealed a range of morphological subtypes of bipolar, amacrine, and ganglion cells. There are at least seven subtypes of bipolar cells. Those subtypes in which the somata were high (sclerad) in the inner nuclear layer (3 subtypes) had axon terminals low (vitread) in the inner plexiform layer, and those with somata low in the inner nuclear layer (4 subtypes) had axon terminals high in the inner plexiform layer. The bipolar subtypes with high axon terminals made flat contacts with receptor cells, whereas all but one of the bipolar subtypes with low axon terminals made ribbon‐related contacts with receptor cells. There are at least five subtypes of amacrine cells. The two subtypes which the Golgi method revealed most frequently were a broad‐field, unistratified neuron with a dendritic spread in excess of 1,000 m̈m and a narrow‐field, diffuse neuron with a dendritic spread of about 30 m̈m. The broad‐field, unistratified cell had the lowest proportion of amacrine vs. bipolar cell synaptic input of the amacrine subtypes (43%), whereas the narrow‐field, diffuse cell had one of the greatest proportions of amacrine cell input (96%). There are at least 15 subtypes of ganglion cells. The proportion of synaptic inputs to these cells ranged from 21% to 100% amacrine cell synapses. An attempt has been made to relate this new knowledge of retinal circuitry to the physiological output of the ganglion cells.