The DOI matches its Crossref record; 5 of the 5 references it cites were found in a registry or an index.
Lateral interactions in the outer retina
Open accessAbstract
Lateral interactions in the outer retina, particularly negative feedback from horizontal cells to cones and direct feed-forward input from horizontal cells to bipolar cells, play a number of important roles in early visual processing, such as generating center-surround receptive fields that enhance spatial discrimination. These circuits may also contribute to post-receptoral light adaptation and the generation of color opponency. In this review, we examine the contributions of horizontal cell feedback and feed-forward pathways to early visual processing. We begin by reviewing the properties of bipolar cell receptive fields, especially with respect to modulation of the bipolar receptive field surround by the ambient light level and to the contribution of horizontal cells to the surround. We then review evidence for and against three proposed mechanisms for negative feedback from horizontal cells to cones: 1) GABA release by horizontal cells, 2) ephaptic modulation of the cone pedicle membrane potential generated by currents flowing through hemigap junctions in horizontal cell dendrites, and 3) modulation of cone calcium currents (ICa) by changes in synaptic cleft proton levels. We also consider evidence for the presence of direct horizontal cell feed-forward input to bipolar cells and discuss a possible role for GABA at this synapse. We summarize proposed functions of horizontal cell feedback and feed-forward pathways. Finally, we examine the mechanisms and functions of two other forms of lateral interaction in the outer retina: negative feedback from horizontal cells to rods and positive feedback from horizontal cells to cones.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
The contrast sensitivity of retinal ganglion cells of the cat
Enroth-Cugell, C., & Robson, J. G. (1966) · The Journal of Physiology · doi:10.1113/jphysiol.1966.sp008107 · Cited by 2,625
Predictive coding: a fresh view of inhibition in the retina
Srinivasan, M. V., Laughlin, S. B., & Dubs, A. (1982) · Proceedings of the Royal Society of London. Series B. Biological Sciences · doi:10.1098/rspb.1982.0085 · Cited by 1,042 · cited 4×
“It has been proposed that the ability of bipolar and ganglion cells to report fine spatial details about the visual environment results from subtraction of the surround signal (which pools visual information from a relatively wide area) from the center signal (which responds to local illumination) (Ratliff and Hartlin…”
BackgroundInfluentialMechanisms underlying development of visual maps and receptive fields
Huberman, A. D., Feller, M. B., & Chapman, B. (2008) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.31.060407.125533 · Cited by 628
Johnson, J., Tian, N., Caywood, M. S., Reimer, R. J., Edwards, R. H., & Copenhagen, D. R. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-02-00518.2003 · Cited by 197
Carbenoxolone Inhibition of Voltage-Gated Ca Channels and Synaptic Transmission in the Retina
Vessey, J. P., Lalonde, M. R., Mizan, H. A., Welch, N. C., Kelly, M. E. M., & Barnes, S. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00148.2004 · Cited by 178
Cited by
Sterling, P., & Laughlin, S. (2015) · doi:10.7551/mitpress/9780262028707.001.0001 · Cited by 482
Retinal output changes qualitatively with every change in ambient illuminance
Tikidji-Hamburyan, A., Reinhard, K., Seitter, H., Hovhannisyan, A., Procyk, C. A., Allen, A. E., Schenk, M., Lucas, R. J., & Münch, T. A. (2015) · Nature Neuroscience · doi:10.1038/nn.3891 · Cited by 134
How diverse retinal functions arise from feedback at the first visual synapse
Drinnenberg, A., Franke, F., Morikawa, R. K., Jüttner, J., Hillier, D., Hantz, P., Hierlemann, A., Azeredo da Silveira, R., & Roska, B. (2018) · Neuron · doi:10.1016/j.neuron.2018.06.001 · Cited by 61
Metadata
- Authors
- Thoreson, W. B., & Mangel, S. C.
- Venue
- Progress in Retinal and Eye Research
- Publisher
- Elsevier BV
- Published
- 2012-09
- Volume
- 31
- Issue
- 5
- Pages
- 407-441
- ISSN
- 1350-9462 (ISSN-L)
- OpenAlex
- W2071567206
- Cited by
- 262
- References
- 5
- FWCI
- 6.51
- Type
- journal article
- Language
- en
- Open access
- green
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
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
