Dm. Dacey, CIRCUITRY FOR COLOR CODING IN THE PRIMATE RETINA, Proceedings of the National Academy of Sciences of the United Statesof America, 93(2), 1996, pp. 582-588
Human color vision starts with the signals from three cone photorecept
or types, maximally sensitive to long (L-cone), middle (M-cone), and s
hort (S-cone) wavelengths. Within the retina these signals combine in
an antagonistic way to form red-green and blue-yellow spectral opponen
t pathways, In the classical model this antagonism is thought to arise
from the convergence of cone type-specific excitatory and inhibitory
inputs to retinal ganglion cells, The circuitry for spectral opponency
is now being investigated using an in vitro preparation of the macaqu
e monkey retina, Intracellular recording and staining has shown that b
lue-ON/yellow-OFF opponent responses arise from a distinctive bistrati
fied ganglion cell type. Surprisingly, this cone opponency appears to
arise by dual excitatory cone bipolar cell inputs: an ON bipolar cell
that contacts only S-cones and an OFF bipolar cell that contacts L- an
d M-cones, Red-green spectral opponency has long been linked to the mi
dget ganglion cells, but an underlying mechanism remains unclear. For
example, receptive field mapping argues for segregation of L- and M-co
ne signals to the midget cell center and surround, but horizontal cell
interneurons, believed to generate the inhibitory surround, lack oppo
nency and cannot contribute selective L- or M-cone input to the midget
cell surround. The solution to this color puzzle no doubt lies in the
great diversity of cell types in the primate retina that still await
discovery and analysis.