U. Grunert et al., IMMUNOCYTOCHEMICAL ANALYSIS OF BIPOLAR CELLS IN THE MACAQUE MONKEY RETINA, Journal of comparative neurology, 348(4), 1994, pp. 607-627
Transfer of visual information from photoreceptors to ganglion cells w
ithin the retina is mediated by specialized groups of bipolar cells. A
t least 10 different morphological types of bipolar cells have been di
stinguished in Golgi studies of primate retina. In the present study,
bipolar cell populations in the macaque monkey retina were identified
by their differential immunoreactivity to a spectrum of antibody marke
rs. This enabled their spatial density and photoreceptor connections t
o be analysed. An antibody against the beta isozyme of protein kinase
C (PKCA(beta)) labelled many cone bipolar cells. Invaginating (presume
d ON) cone bipolar cells and rod bipolar cells were prefentially label
led with a monoclonal antibody raised against rabbit olfactory bulb. F
lat (presumed OFF) bipolar cells were labelled with an antiserum again
st the glutamate transporter protein (GLT-1). Different populations of
diffuse cone bipolar cells, which contact 5-10 cones, could be distin
guished. The GLT-1 antiserum preferentially labelled the flat diffuse
bipolar cell type DB2 (Boycott and Wassle, 1991, fur. J. Neurosci. 3:1
069-1088) as well as flat midget bipolar cells. Antibodies to calbindi
n (CaBP D-28K) labelled the flat diffuse bipolar cell type DB3 and (po
ssibly) the invaginating diffuse bipolar cell type DB5. An antibody ag
ainst the cr, isozyme of PKC labelled an invaginating diffuse bipolar
cell type (DB4) as well as rod bipolar cells. Comparison of the spatia
l density of cone bipolar cell populations with that of photoreceptors
suggests that each bipolar cell class provides a complete coverage of
the cone array (each cone is contacted by at least one member of ever
y bipolar cell class). These results support the classification scheme
of Boycott and Wassle (1991) by showing that different diffuse bipola
r cell classes express different patterns of immunoreactivity, and the
y reinforce the view that different spatial and temporal components of
the signal from the photoreceptor array are processed in parallel wit
hin the primate retina. (C) 1994 Wiley-Liss, Inc.