Marshak D, Ariel M, Brown E
Biological Laboratories, Harvard University, Cambridge, MA 02138.
Exp Eye Res. 1988 Jun;46(6):965-78. doi: 10.1016/s0014-4835(88)80048-4.
Retinal ganglion cells in the goldfish were labeled by retrograde transport of horseradish peroxidase, and areas near the optic disk where the dendrites appeared to be completely filled were analyzed by electron microscopy. Only 6% of their inputs were ribbon synapses from bipolar cells; the other 94% of the inputs were conventional synapses mostly or entirely from amacrine cells. There were three strata of the inner plexiform layer with high densities of inputs to ganglion cells, the first centered at approx. 50% and the second at approx. 80% of the inner plexiform layer depth, as measured from the ganglion cell layer to the inner nuclear layer. These two strata comprised 25% of the volume but contained 41% of the inputs to ganglion cells. There were also two strata with very low densities of ganglion cell inputs located near the boundaries of the inner plexiform layer, from 0- to 15% and 90- to 100% of the depth. These strata, which also comprised 25% of the volume, contained only 7% of the inputs to retinal ganglion cells. These strata near the boundaries of the inner plexiform layer also contained 81% of the processes with large, dense-cored vesicles characteristic of peptidergic neurons. We concluded that each of the two sublaminae, a and b, identified previously by physiological criteria, could be further divided into at least two strata, one near the boundary of the inner plexiform layer with abundant peptidergic terminals and very few ganglion cell synapses and another near the center of the inner plexiform layer with numerous ganglion cell synapses. We also propose a hypothesis that could explain the functions of these additional strata.
