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Immunocytochemical analysis of bipolar cells in the macaque monkey retina
Abstract
Transfer of visual information from photoreceptors to ganglion cells within the retina is mediated by specialized groups of bipolar cells. At least 10 different morphological types of bipolar cells have been distinguished 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 markers. This enabled their spatial density and photoreceptor connections to be analysed. An antibody against the β isozyme of protein kinase C (PKCA β) labelled many cone bipolar cells. Invaginating (presumed ON) cone bipolar cells and rod bipolar cells were prefentially labelled with a monoclonal antibody raised against rabbit olfactory bulb. Flat (presumed OFF) bipolar cells were labelled with an antiserum against the glutamate transporter protein (GLT‐1). Different populations of diffuse cone bipolar cells, which contact 5–10 cones, could be distinguished. The GLT‐1 artiserum preferentially labelled the flat diffuse bipolar cell type DB2 (Boycott and Wässle, 1991, Eur. J. Neurosci. 3:1069–1088) as well as flat midget bipolar cells. Antibodies to calbindin (CaBP D‐28K) labelled the flat diffuse bipolar cell type DB3 and (possibly) the invaginating diffuse bipolar cell type DB5. An antibody against the α isozyme of PKC labelled an invaginating diffuse bipolar cell type (DB4) as well as rod bipolar cells. Comparison of the spatial 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 every bipolar cell class). These results support the classification scheme of Boycott and Wässle (1991) by showing that different diffuse bipolar cell classes express different patterns of immunoreactivity, and they reinforce the view that different spatial and temporal components of the signal from the photoreceptor array are processed in parallel within the primate retina. © 1994 Wiley‐Liss, Inc.
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Citations
Cited by
The fundamental plan of the retina
Masland, R. H. (2001) · Nature Neuroscience · doi:10.1038/nn0901-877 · Cited by 1,237
Neural remodeling in retinal degeneration
Marc, R. E., Jones, B. W., Watt, C. B., & Strettoi, E. (2003) · Progress in Retinal and Eye Research · doi:10.1016/s1350-9462(03)00039-9 · Cited by 867
Immunocytochemical analysis of the mouse retina
Haverkamp, S., & W�ssle, H. (2000) · The Journal of Comparative Neurology · doi:10.1002/1096-9861(20000814)424:1<1::aid-cne1>3.0.co;2-v · Cited by 710
Self-citationImmunocytochemical identification of cone bipolar cells in the rat retina
Euler, T., & Wässle, H. (1995) · Journal of Comparative Neurology · doi:10.1002/cne.903610310 · Cited by 347
Self-citationThe SLC1 high-affinity glutamate and neutral amino acid transporter family
Kanai, Y., Clémençon, B., Simonin, A., Leuenberger, M., Lochner, M., Weisstanner, M., & Hediger, M. A. (2013) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2013.01.001 · Cited by 329
Metadata
- Authors
- Grünert, U., Martin, P. R., & Wässle, H.
- Venue
- Journal of Comparative Neurology
- Publisher
- Wiley
- Published
- 1994-10-22
- Volume
- 348
- Issue
- 4
- Pages
- 607-627
- ISSN
- 0021-9967 (ISSN-L)
- 1096-9861
- OpenAlex
- W2112540246
- Cited by
- 194
- References
- 0
- FWCI
- 2.94
- Type
- journal article
- Language
- en
- Open access
- closed
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