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
Cited by
Sorted by citations
Items 201–225 of 225
Lux, U. T., Ehrenberg, J., Joachimsthaler, A., Atorf, J., Pircher, B., Reim, K., Kremers, J., Gießl, A., & Brandstätter, J. H. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22158131 · Cited by 6
He, T., Mortensen, X. M., Wang, P., & Tian, N. (2017) · PLoS ONE · doi:10.1371/journal.pone.0175522 · Cited by 6
Murphy‐Baum, B. L., Schwartz, G. W., & Awatramani, G. B. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-819896-4.00012-3 · Cited by 5
Slaughter, M. M. (1990) · Springer eBooks · doi:10.1007/978-1-4612-3406-7_3 · Cited by 5
Chen, J., Yan, L., Huang, J., Wang, W., Wei, Y., Li, Y.-Q., Kaneko, T., & Wu, S. (2013) · Neuroscience Letters · doi:10.1016/j.neulet.2013.05.054 · Cited by 5
“[3] N.”
BackgroundFoley, P., Hughes, P., Bradford, H. F., Ghatei, M. A., Khandanian, N., & Bloom, S. R. (1992) · Neuropeptides · doi:10.1016/0143-4179(92)90080-g · Cited by 5
Calcium Channels in Retinal Function and DiseasePreprint
Williams, B., Maddox, W., & Lee, A. (2021) · Preprints.org · doi:10.20944/preprints202101.0466.v1 · Cited by 5
Modeling Starburst Cells’ GABAB Receptors and Their Putative Role in Motion Sensitivity
Grzywacz, N. M., & Zucker, C. L. (2006) · Biophysical Journal · doi:10.1529/biophysj.105.072256 · Cited by 4
“Rc1,n,c2 (t) = βn,c2 1 + exp (−αn (Vc (t)− θn)) , (2)”
Distributed Parallel Processing in Retinal Amacrine Cells
Diamond, J. S., & Grimes, W. N. (2013) · Springer series in computational neuroscience · doi:10.1007/978-1-4614-8094-5_12 · Cited by 4
Famiglietti, E. V. (2016) · Visual Neuroscience · doi:10.1017/s0952523815000358 · Cited by 3
A Neuron for Velocity Detection Based on Inhibitory Mechanism in Retina Ganglion
Han, M., Todo, Y., & Tang, Z. (2021) · International Conference on Artificial Intelligence and Big Data (ICAIBD) · doi:10.1109/icaibd51990.2021.9459044 · Cited by 3
Potassium-evoked directionally selective responses from rabbit retinal ganglion cells
Jensen, R. J. (1996) · Visual Neuroscience · doi:10.1017/s0952523800008592 · Cited by 3
A review of the neurophysiology of the turtle retina III. Amacrine and ganglion cells
Westbrook, A. M. (1994) · Clinical and Experimental Optometry · doi:10.1111/j.1444-0938.1994.tb06538.x · Cited by 3
Computation of motion direction in the vertebrate retina
Euler, T., & Hausselt, S. E. (2012) · e-Neuroforum · doi:10.1007/s13295-012-0033-x · Cited by 1
Synapse formation in the developing vertebrate retina
Huang, X., Ledesma, H. A., & Wei, W. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-823672-7.00009-0 · Cited by 1
Effects of GABA Receptor Agonists on Cholinergic Amacrine Cells in the Rabbit Retina
Neal, M. J. (1995) · Springer eBooks · doi:10.1007/978-1-4757-9362-8_8 · Cited by 1
Kim, H.-C., Suh, W., Moon, J.-I., & Choi, K. R. (2008) · Journal of the Korean Ophthalmological Society · doi:10.3341/jkos.2008.49.2.340
Retinal Characterization of the Thy1-GCaMP3 Transgenic Mouse Line
Blandford, S. N. (2016) · DalSpace (Dalhousie University)
but not of GABA, in cultured retina cells
Santos, P. F., Caramelo, O. L., & Carvalho, A. P. (2000)
Carrero, L., Antequera, D., Alcalde, I., Megías, D., Figueiro‐Silva, J., Merayo-Lloves, J., Municio, C., & Carro, E. (2024) · Figshare · doi:10.6084/m9.figshare.26579723
Carrero, L., Antequera, D., Alcalde, I., Megías, D., Figueiro‐Silva, J., Merayo-Lloves, J., Municio, C., & Carro, E. (2024) · Figshare · doi:10.6084/m9.figshare.26579729
Carrero, L., Antequera, D., Alcalde, I., Megías, D., Figueiro‐Silva, J., Merayo-Lloves, J., Municio, C., & Carro, E. (2024) · Figshare · doi:10.6084/m9.figshare.26579732
Carrero, L., Antequera, D., Alcalde, I., Megías, D., Figueiro‐Silva, J., Merayo-Lloves, J., Municio, C., & Carro, E. (2024) · Figshare · doi:10.6084/m9.figshare.26579726
[T4, T3, TSH, HGH in anorexia nervosa--TRH-LH-RH loading test].
Niimi, H., Makino, S., Sasaki, N., NAKAMURA, Y., & Mayama, K. (1977) · PubMed
Lawson (1996) · doi:10.1002/(sici)1096-9861(19960212)365:3
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