The DOI matches its Crossref record; 45 of the 45 references it cites were found in a registry or an index.
Cholinergic amacrine cells of the rabbit retina contain glutamate decarboxylase and gamma-aminobutyrate immunoreactivity
Open accessAbstract
The transmitters acetylcholine and gamma-aminobutyrate (GABA) play critical roles in the formation of receptive-field properties of retinal ganglion cells. In rabbit retina, cholinergic amacrine and displaced amacrine cells were identified by immunohistochemical staining for the enzyme choline acetyltransferase and by their avid accumulation of the fluorescent dye 4',6-diamidino-2-phenylindole. Several GABA-immunoreactive and glutamate decarboxylase-immunoreactive cell types, including a prominent population of small, round amacrine and displaced amacrine cells, were also identified. Double-label experiments demonstrated that all amacrine and displaced amacrine cells that prominently accumulate 4',6-diamidino-2-phenylindole contain GABA and glutamate decarboxylase immunoreactivity. However, not all GABA-immunoreactive cells accumulate this dye. Quantitative analysis of the ganglion cell layer of whole mount preparations of the retina showed that choline acetyltransferase-immunoreactive cells and the majority of GABA-immunoreactive cells have a small, round shape and similar cell density profiles that parallel that of displaced amacrine cells. These studies establish that cholinergic cells are a major subpopulation of GABA-immunoreactive amacrine and displaced amacrine cells. The role these cells have in the formation of ganglion cell receptive-field properties may be parsimoniously explained by an excitatory postsynaptic action mediated by acetylcholine and an inhibitory presynaptic action mediated by GABA.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The text we found for this paper looks like another document, so the self-check wasn’t run.
Citations
Cites
Hökfelt, T. G. M., Johansson, O., Ljungdahl, Å., Lundberg, J. M., & Schultzberg, M. (1980) · Nature · doi:10.1038/284515a0 · Cited by 1,552
First visualization of glutamate and GABA in neurones by immunocytochemistry
Storm‐Mathisen, J., Leknes, A. K., Bore, A. T., Vaaland, J. L., Edminson, P. D., Haug, F. Š., & Ottersen, O. P. (1983) · Nature · doi:10.1038/301517a0 · Cited by 869
Houser, C. R., Crawford, G. D., Barber, R. P., Salvaterra, P. M., & Vaughn, J. E. (1983) · Brain Research · doi:10.1016/0006-8993(83)91312-4 · Cited by 748
Presynaptic regulation of neurotransmitter release in the brain: Facts and hypothesis
Chesselet, M.-F. (1984) · Neuroscience · doi:10.1016/0306-4522(84)90058-7 · Cited by 577
Oertel, W., Schmechel, D. E., Tappaz, M., & Kopin, I. J. (1981) · Neuroscience · doi:10.1016/0306-4522(81)90113-5 · Cited by 419
Kosaka, T., Tauchi, M., & Dahl, J. L. (1988) · Experimental Brain Research · doi:10.1007/bf00247609 · Cited by 417
The shape and arrangement of the cholinergic neurons in the rabbit retina
Tauchi, M., & Masland, R. H. (1984) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1984.0085 · Cited by 385
Famiglietti, E. V. (1983) · Brain Research · doi:10.1016/0006-8993(83)91293-3 · Cited by 294
Caldwell, J. H., Daw, N. W., & Wyatt, H. J. (1978) · The Journal of Physiology · doi:10.1113/jphysiol.1978.sp012233 · Cited by 290
Autoradiographic identification of acetylcholine in the rabbit retina.
Masland, R. H., & Mills, J. W. (1979) · The Journal of Cell Biology · doi:10.1083/jcb.83.1.159 · Cited by 286
Cholinergic amacrine cells in the rat retina
Voigt, T. (1986) · Journal of Comparative Neurology · doi:10.1002/cne.902480103 · Cited by 284
Pharmacological analysis of directionally sensitive rabbit retinal ganglion cells
Ariel, M., & Daw, N. W. (1982) · The Journal of Physiology · doi:10.1113/jphysiol.1982.sp014105 · Cited by 282
Ehinger, B., & FALCK, B. (1971) · Brain Research · doi:10.1016/0006-8993(71)90314-3 · Cited by 277
Responses to acetylcholine of ganglion cells in an isolated mammalian retina
Masland, R. H., & Ames, A. (1976) · Journal of Neurophysiology · doi:10.1152/jn.1976.39.6.1220 · Cited by 256
GABA-like immunoreactivity in the vertebrate retina: a species comparison
Ogilvie, J. M., Yazulla, S., & Studholme, K. M. (1986) · Experimental Eye Research · doi:10.1016/0014-4835(86)90052-7 · Cited by 233
Ruskell, G. L. (1987) · Comparative Biochemistry and Physiology Part A Physiology · doi:10.1016/0300-9629(87)90162-9 · Cited by 228
The functions of acetylcholine in the rabbit retina
Masland, R. H., Mills, J. W., & Cassidy, C. (1984) · Proceedings of the Royal Society of London. Series B. Biological Sciences · doi:10.1098/rspb.1984.0086 · Cited by 200
‘Coronate’ amacrine cells in the rabbit retina have the ‘starburst’ dendritic morphology
Di, V. (1984) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1984.0016 · Cited by 193
Kosaka, T., Kosaka, K., Hataguchi, Y., Nagatsu, I., Wu, J., Ottersen, O. P., Storm‐Mathisen, J., & Hama, K. (1987) · Experimental Brain Research · doi:10.1007/bf00236215 · Cited by 191
Masland, R. H., Mills, J. W., & Hayden, S. (1984) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1984.0084 · Cited by 190
Baughman, R. W., & Bader, C. R. (1977) · Brain Research · doi:10.1016/0006-8993(77)90684-9 · Cited by 189
Vaney, D. I., Peichl, L., & Boycott, B. B. (1981) · The Journal of Comparative Neurology · doi:10.1002/cne.901990305 · Cited by 189
Brandon, C. J. (1985) · Brain Research · doi:10.1016/0006-8993(85)90806-6 · Cited by 166
Brandon, C. J., Lam, D., & Wu, J. (1979) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.76.7.3557 · Cited by 160
Amacrine cells in the ganglion cell layer of the cat retina
Wässle, H., Chun, M., & Müller, F. U. (1987) · The Journal of Comparative Neurology · doi:10.1002/cne.902650308 · Cited by 154
Effects of cholinergic drugs on receptive field properties of rabbit retinal ganglion cells
Ariel, M., & Daw, N. W. (1982) · The Journal of Physiology · doi:10.1113/jphysiol.1982.sp014104 · Cited by 153
Monoclonal antibodies demonstrating GABA-like immunoreactivity
Matute, C., & Streit, P. (1986) · Histochemistry and Cell Biology · doi:10.1007/bf00493380 · Cited by 148
Substance P-immunoreactive retinal ganglion cells and their central axon terminals in the rabbit
Brecha, N. C., Johnson, D., Bolz, J., Sharma, S. C., Parnavelas, J. G., & Lieberman, A. R. (1987) · Nature · doi:10.1038/327155a0 · Cited by 143
Vaney, D. I. (1980) · The Journal of Comparative Neurology · doi:10.1002/cne.901890202 · Cited by 141
Monoclonal Antibodies and Polyvalent Antiserum to Chicken Choline Acetyltransferase
Johnson, C. D., & Epstein, M. L. (1986) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1986.tb13064.x · Cited by 139
GABA and neuropeptides in the CNS
Björklund, A., & Hökfelt, T. G. M. (1985) · Elsevier eBooks · Cited by 133
Almost all ganglion cells in the rabbit retina project to the superior colliculus
Vaney, D. I., Peichl, L., Wässle, H., & Illing, R. (1981) · Brain Research · doi:10.1016/0006-8993(81)90476-5 · Cited by 130
Masland, R. H., & Livingstone, C. J. (1976) · Journal of Neurophysiology · doi:10.1152/jn.1976.39.6.1210 · Cited by 130
Massey, S. C., & Neal, M. J. (1979) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1979.tb11062.x · Cited by 117
Acetylcholine Synthesis by Displaced Amacrine Cells
Hayden, S., Mills, J. W., & Masland, R. M. (1980) · Science · doi:10.1126/science.7433984 · Cited by 114
Agardh, E., Bruun, A., Ehinger, B., Ekström, P., Veen, T. V., & Wu, J. (1987) · The Journal of Comparative Neurology · doi:10.1002/cne.902580411 · Cited by 111
Coronate cells: Displaced amacrines of the rabbit retina?
Hughes, A., & Vaney, D. I. (1980) · The Journal of Comparative Neurology · doi:10.1002/cne.901890110 · Cited by 98
A tonic gamma-aminobutyric acid-mediated inhibition of cholinergic amacrine cells in rabbit retina
Massey, S., & Redburn, D. (1982) · Journal of Neuroscience · doi:10.1523/jneurosci.02-11-01633.1982 · Cited by 92
Review: Acetylcholine as a neurotransmitter in the vertebrate retina
Hutchins, J. B. (1987) · Experimental Eye Research · doi:10.1016/s0014-4835(87)80075-1 · Cited by 80
Number and distribution of putative cholinergic neurons in the cat retina
Schmidt, M., Wässle, H., & Humphrey, M. F. (1985) · Neuroscience Letters · doi:10.1016/0304-3940(85)90137-5 · Cited by 77
Cunningham, J. R., & Neal, M. J. (1983) · The Journal of Physiology · doi:10.1113/jphysiol.1983.sp014598 · Cited by 74
Brandon, C. J. (1987) · Brain Research · doi:10.1016/0006-8993(87)91426-0 · Cited by 59
Colocalization of GAD‐like immunoreactivity and 3H‐GABA uptake in amacrine cells of rabbit retina
Ogilvie, J. M., & Yazulla, S. (1985) · The Journal of Comparative Neurology · doi:10.1002/cne.902400407 · Cited by 47
Retinal Gaba neuron labelling with [3H]isoguvacine in different species
Agardh, E., & Ehinger, B. (1983) · Experimental Eye Research · doi:10.1016/0014-4835(83)90007-6 · Cited by 30
Massey, S. C., & Redburn, D. A. (1985) · Brain Research · doi:10.1016/0006-8993(85)91052-2 · Cited by 21
Cited by
Sorted by citations
Topography of ganglion cells in human retina
Curcio, C. A., & Allen, K. A. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.903000103 · Cited by 1,849
Periaqueductal gray matter projections to midline and intralaminar thalamic nuclei of the rat
Krout, K. E., & Loewy, A. D. (2000) · The Journal of Comparative Neurology · doi:10.1002/1096-9861(20000814)424:1 · Cited by 180
Directionally selective calcium signals in dendrites of starburst amacrine cells
Euler, T., Detwiler, P. B., & Denk, W. T. (2002) · Nature · doi:10.1038/nature00931 · Cited by 588
“How is the directional motion information used after it has been generated in the starburst cell dendrite? Starburst amacrine cells contain and release GABA and acetylcholine (ACh”
BackgroundChapter 2 The mosaic of amacrine cells in the mammalian retina
Vaney, D. I. (1990) · Progress in Retinal Research · doi:10.1016/0278-4327(90)90004-2 · Cited by 372
Mechanisms and circuitry underlying directional selectivity in the retina
Fried, S. I., Münch, T. A., & Werblin, F. S. (2002) · Nature · doi:10.1038/nature01179 · Cited by 368
Metadata
- Authors
- Brecha, N., Johnson, D., Peichl, L., & Wässle, H.
- Affiliations
- University of California, Los Angeles (US)
- ORCID
- Peichl, L
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 1988-08
- Volume
- 85
- Issue
- 16
- Pages
- 6187-6191
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC281930
- OpenAlex
- W2019521144
- Cited by
- 225
- References
- 44
- Citations by year
- 2024: 6 · 2023: 2 · 2022: 2 · 2021: 6 · 2020: 7 · 2019: 1 · 2018: 3 · 2017: 5 · 2016: 5 · 2015: 4 · 2014: 2 · 2013: 4 · 2012: 6
- FWCI
- 4.40
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Eye Institute (R01EY004067, EY 04067)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Health Sciences › Medicine › Ophthalmology › Retinal Development and Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Nicotinic Acetylcholine Receptors Study
- Keywords
- cholinergic amacrine cells, displaced amacrine cells, glutamic acid decarboxylase, GABA, choline acetyltransferase, retinal ganglion cells, receptive fields, acetylcholine, GABAergic inhibition, cholinergic inhibition, rabbit retina
- MeSH terms
- Acetylcholine, Animals, Choline O-Acetyltransferase, gamma-Aminobutyric Acid, Glutamate Decarboxylase, Horseradish Peroxidase, Indoles, Parasympathetic Nervous System, Rabbits, Retina
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review