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Hierarchical retinal computations rely on hybrid chemical-electrical signaling

https://doi.org/10.1016/j.celrep.2023.112030

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/cne.20304openalex-snapshot

Quantitative analysis of neuronal morphologies in the mouse retina visualized by using a genetically directed reporter

inferredcites →https://doi.org/10.1002/cne.21126openalex-snapshot

Populations of wide‐field amacrine cells in the mouse retina

inferredcites →https://doi.org/10.1002/cne.23752openalex-snapshot

Morphology and connectivity of the small bistratified A8 amacrine cell in the mouse retina

inferredcites →https://doi.org/10.1006/scdb.1998.0235openalex-snapshot

The modulation of intercellular coupling in the retina

inferredcites →https://doi.org/10.1016/j.cell.2014.06.047openalex-snapshot

Type II Cadherins Guide Assembly of a Direction-Selective Retinal Circuit

inferredcites →https://doi.org/10.1016/j.cell.2016.07.054openalex-snapshot

Comprehensive Classification of Retinal Bipolar Neurons by Single-Cell Transcriptomics

inferredcites →https://doi.org/10.1016/j.celrep.2016.02.001openalex-snapshot

Analogous Convergence of Sustained and Transient Inputs in Parallel On and Off Pathways for Retinal Motion Computation

inferredcites →https://doi.org/10.1016/j.celrep.2016.04.069openalex-snapshot

Two Pairs of ON and OFF Retinal Ganglion Cells Are Defined by Intersectional Patterns of Transcription Factor Expression

inferredcites →https://doi.org/10.1016/j.celrep.2020.108382openalex-snapshot

Gbx2 Identifies Two Amacrine Cell Subtypes with Distinct Molecular, Morphological, and Physiological Properties

inferredcites →https://doi.org/10.1016/j.celrep.2022.110412openalex-snapshot

Parallel processing in active dendrites during periods of intense spiking activity

inferredcites →https://doi.org/10.1016/j.cub.2012.11.006openalex-snapshot

Spikes in Mammalian Bipolar Cells Support Temporal Layering of the Inner Retina

inferredcites →https://doi.org/10.1016/j.cub.2022.02.048openalex-snapshot

Orientation and direction tuning align with dendritic morphology and spatial connectivity in mouse visual cortex

inferredcites →https://doi.org/10.1016/j.jphs.2019.03.006openalex-snapshot

Dopaminergic modulation of retinal processing from starlight to sunlight

inferredcites →https://doi.org/10.1016/j.neuron.2009.12.009openalex-snapshot

Eye Smarter than Scientists Believed: Neural Computations in Circuits of the Retina

inferredcites →https://doi.org/10.1016/j.neuron.2013.02.014openalex-snapshot

Ambient Illumination Toggles a Neuronal Circuit Switch in the Retina and Visual Perception at Cone Threshold

inferredcites →https://doi.org/10.1016/j.neuron.2013.08.005openalex-snapshot

The First Stage of Cardinal Direction Selectivity Is Localized to the Dendrites of Retinal Ganglion Cells

inferredcites →https://doi.org/10.1016/j.neuron.2013.11.029openalex-snapshot

The Projective Field of Retinal Bipolar Cells and Its Modulation by Visual Context

inferredcites →https://doi.org/10.1016/j.neuron.2014.02.037openalex-snapshot

The Synaptic and Circuit Mechanisms Underlying a Change in Spatial Encoding in the Retina

inferredcites →https://doi.org/10.1016/j.neuron.2015.02.035openalex-snapshot

Specific Wiring of Distinct Amacrine Cells in the Directionally Selective Retinal Circuit Permits Independent Coding of Direction and Size

inferredcites →https://doi.org/10.1016/j.neuron.2015.09.033openalex-snapshot

Orientation Selectivity Sharpens Motion Detection in Drosophila

inferredcites →https://doi.org/10.1016/j.neuron.2016.03.012openalex-snapshot

Nonlinear Spatiotemporal Integration by Electrical and Chemical Synapses in the Retina

inferredcites →https://doi.org/10.1016/j.neuron.2016.04.041openalex-snapshot

A Central Role for Mixed Acetylcholine/GABA Transmission in Direction Coding in the Retina

inferredcites →https://doi.org/10.1016/j.neuron.2018.08.021openalex-snapshot

Gap Junctions Contribute to Differential Light Adaptation across Direction-Selective Retinal Ganglion Cells

inferredcites →https://doi.org/10.1016/j.neuron.2019.04.002openalex-snapshot

A Retinal Circuit Generating a Dynamic Predictive Code for Oriented Features

inferredcites →https://doi.org/10.1016/j.neuron.2021.03.015openalex-snapshot

Nonlinear spatial integration in retinal bipolar cells shapes the encoding of artificial and natural stimuli

inferredcites →https://doi.org/10.1016/j.neuron.2021.07.008openalex-snapshot

Direction selectivity in retinal bipolar cell axon terminals

inferredcites →https://doi.org/10.1016/s0021-9258(19)50280-0openalex-snapshot

Molecular characterization of a novel retinal metabotropic glutamate receptor mGluR6 with a high agonist selectivity for L-2-amino-4-phosphonobutyrate

inferredcites →https://doi.org/10.1016/s0042-6989(00)00039-0openalex-snapshot

Center surround receptive field structure of cone bipolar cells in primate retina

inferredcites →https://doi.org/10.1016/s0896-6273(00)00158-6openalex-snapshot

Bipolar Cells Use Kainate and AMPA Receptors to Filter Visual Information into Separate Channels

inferredcites →https://doi.org/10.1017/s0952523809990137openalex-snapshot

Receptive field properties of ON- and OFF-ganglion cells in the mouse retina

inferredcites →https://doi.org/10.1017/s0952523898153038openalex-snapshot

Distinguishing direction selectivity from orientation selectivity in the rabbit retina

inferredcites →https://doi.org/10.1038/20187openalex-snapshot

Synaptic calcium transients in single spines indicate that NMDA receptors are not saturated

inferredcites →https://doi.org/10.1038/303537a0openalex-snapshot

Bipolar cells in the mudpuppy retina use an excitatory amino acid neurotransmitter

inferredcites →https://doi.org/10.1038/377734a0openalex-snapshot

Differential properties of two gap junctional pathways made by AII amacrine cells

inferredcites →https://doi.org/10.1038/nature06739openalex-snapshot

Molecular identification of a retinal cell type that responds to upward motion

inferredcites →https://doi.org/10.1038/nature12346openalex-snapshot

Connectomic reconstruction of the inner plexiform layer in the mouse retina

inferredcites →https://doi.org/10.1038/nature16468openalex-snapshot

The functional diversity of retinal ganglion cells in the mouse

inferredcites →https://doi.org/10.1038/nature18609openalex-snapshot

Species-specific wiring for direction selectivity in the mammalian retina

inferredcites →https://doi.org/10.1038/nature21394openalex-snapshot

Inhibition decorrelates visual feature representations in the inner retina

inferredcites →https://doi.org/10.1038/nature22818openalex-snapshot

A retinal code for motion along the gravitational and body axes

inferredcites →https://doi.org/10.1038/nn.2389openalex-snapshot

Approach sensitivity in the retina processed by a multifunctional neural circuit

inferredcites →https://doi.org/10.1038/nn.2831openalex-snapshot

Cardinal rules: visual orientation perception reflects knowledge of environmental statistics

inferredcites →https://doi.org/10.1038/nprot.2010.106openalex-snapshot

Two-photon targeted recording of GFP-expressing neurons for light responses and live-cell imaging in the mouse retina

inferredcites →https://doi.org/10.1038/nrn2636openalex-snapshot

The diverse functional roles and regulation of neuronal gap junctions in the retina

inferredcites →https://doi.org/10.1038/nrn3165openalex-snapshot

Direction selectivity in the retina: symmetry and asymmetry in structure and function

inferredcites →https://doi.org/10.1038/nrn3783openalex-snapshot

Retinal bipolar cells: elementary building blocks of vision

inferredcites →https://doi.org/10.1038/s41467-017-01980-9openalex-snapshot

Electrical synapses convey orientation selectivity in the mouse retina

inferredcites →https://doi.org/10.1038/s41467-022-32761-8openalex-snapshot

Classical center-surround receptive fields facilitate novel object detection in retinal bipolar cells

inferredcites →https://doi.org/10.1038/s41467-022-32762-7openalex-snapshot

Center-surround interactions underlie bipolar cell motion sensitivity in the mouse retina

inferredcites →https://doi.org/10.1073/pnas.84.10.3501openalex-snapshot

gamma-Aminobutyric acid exerts a local inhibitory action on the axon terminal of bipolar cells: evidence for negative feedback from amacrine cells.

inferredcites →https://doi.org/10.1073/pnas.95.7.4002openalex-snapshot

The distribution of oriented contours in the real world

inferredcites →https://doi.org/10.1085/jgp.91.2.275openalex-snapshot

Characteristics of bipolar-bipolar coupling in the carp retina.

inferredcites →https://doi.org/10.1113/jp275073openalex-snapshot

Cholinergic excitation complements glutamate in coding visual information in retinal ganglion cells

inferredcites →https://doi.org/10.1113/jphysiol.1959.sp006308openalex-snapshot

Receptive fields of single neurones in the cat's striate cortex

inferredcites →https://doi.org/10.1113/jphysiol.1962.sp006837openalex-snapshot

Receptive fields, binocular interaction and functional architecture in the cat's visual cortex

inferredcites →https://doi.org/10.1113/jphysiol.1973.sp010381openalex-snapshot

Receptive field organization of bipolar and amacrine cells in the goldfish retina

inferredcites →https://doi.org/10.1113/jphysiol.1990.sp017942openalex-snapshot

Spatial organization of the bipolar cell's receptive field in the retina of the tiger salamander.

inferredcites →https://doi.org/10.1113/jphysiol.2007.131763openalex-snapshot

Presynaptic inhibition differentially shapes transmission in distinct circuits in the mouse retina

inferredcites →https://doi.org/10.1146/annurev-neuro-072116-031335openalex-snapshot

Visual Circuits for Direction Selectivity

inferredcites →https://doi.org/10.1146/annurev-vision-082114-035334openalex-snapshot

Functional Circuitry of the Retina

inferredcites →https://doi.org/10.1152/jn.1969.32.3.339openalex-snapshot

Organization of the retina of the mudpuppy, Necturus maculosus. II. Intracellular recording.

inferredcites →https://doi.org/10.1152/jn.1987.58.6.1275openalex-snapshot

Structure of the receptive fields of bipolar cells in the salamander retina

inferredcites →https://doi.org/10.1371/journal.pone.0180091openalex-snapshot

Four alpha ganglion cell types in mouse retina: Function, structure, and molecular signatures

inferredcites →https://doi.org/10.1523/jneurosci.0095-13.2013openalex-snapshot

Orientation-selective Responses in the Mouse Lateral Geniculate Nucleus

inferredcites →https://doi.org/10.1523/jneurosci.0471-20.2020openalex-snapshot

Mouse Retinal Cell Atlas: Molecular Identification of over Sixty Amacrine Cell Types

inferredcites →https://doi.org/10.1523/jneurosci.0564-11.2011openalex-snapshot

Transgenic Mice Reveal Unexpected Diversity of On-Off Direction-Selective Retinal Ganglion Cell Subtypes and Brain Structures Involved in Motion Processing

inferredcites →https://doi.org/10.1523/jneurosci.14-03-01213.1994openalex-snapshot

A novel GABA receptor modulates synaptic transmission from bipolar to ganglion and amacrine cells in the tiger salamander retina

inferredcites →https://doi.org/10.1523/jneurosci.1432-15.2016openalex-snapshot

Synaptic Mechanisms Generating Orientation Selectivity in the ON Pathway of the Rabbit Retina

inferredcites →https://doi.org/10.1523/jneurosci.1590-10.2010openalex-snapshot

Active Roles of Electrically Coupled Bipolar Cell Network in the Adult Retina

inferredcites →https://doi.org/10.1523/jneurosci.1712-15.2015openalex-snapshot

The Synaptic and Morphological Basis of Orientation Selectivity in a Polyaxonal Amacrine Cell of the Rabbit Retina

inferredcites →https://doi.org/10.1523/jneurosci.1810-19.2020openalex-snapshot

Network Architecture of Gap Junctional Coupling among Parallel Processing Channels in the Mammalian Retina

inferredcites →https://doi.org/10.1523/jneurosci.20-04-01519.2000openalex-snapshot

Gap Junctions Linking the Dendritic Network of GABAergic Interneurons in the Hippocampus

inferredcites →https://doi.org/10.1523/jneurosci.20-18-07087.2000openalex-snapshot

Origin of Transient and Sustained Responses in Ganglion Cells of the Retina

inferredcites →https://doi.org/10.1523/jneurosci.2081-10.2010openalex-snapshot

Orientation Selectivity in Rabbit Retinal Ganglion Cells Is Mediated by Presynaptic Inhibition

inferredcites →https://doi.org/10.1523/jneurosci.3965-13.2014openalex-snapshot

Roles of ON Cone Bipolar Cell Subtypes in Temporal Coding in the Mouse Retina

inferredcites →https://doi.org/10.1523/jneurosci.4274-07.2008openalex-snapshot

Disinhibition Combines with Excitation to Extend the Operating Range of the OFF Visual Pathway in Daylight

inferredcites →https://doi.org/10.1523/jneurosci.4442-08.2009openalex-snapshot

Cone Contacts, Mosaics, and Territories of Bipolar Cells in the Mouse Retina

inferredcites →https://doi.org/10.1523/jneurosci.4554-15.2016openalex-snapshot

Cardinal Orientation Selectivity Is Represented by Two Distinct Ganglion Cell Types in Mouse Retina

inferredcites →https://doi.org/10.1523/jneurosci.4984-08.2009openalex-snapshot

Receptive Fields of Retinal Bipolar Cells Are Mediated by Heterogeneous Synaptic Circuitry

inferredcites →https://doi.org/10.1523/jneurosci.5017-13.2014openalex-snapshot

Excitatory Synaptic Inputs to Mouse On-Off Direction-Selective Retinal Ganglion Cells Lack Direction Tuning

inferredcites →https://doi.org/10.3389/fnana.2017.00092openalex-snapshot

Classification of Mouse Retinal Bipolar Cells: Type-Specific Connectivity with Special Reference to Rod-Driven AII Amacrine Pathways

inferredcites →https://doi.org/10.3389/fncir.2018.00011openalex-snapshot

Orientation-Selective Retinal Circuits in Vertebrates

inferredcites →https://doi.org/10.3389/fncir.2018.00090openalex-snapshot

Heterocellular Coupling Between Amacrine Cells and Ganglion Cells

inferredcites →https://doi.org/10.3389/fnmol.2019.00099openalex-snapshot

Gap Junctions in A8 Amacrine Cells Are Made of Connexin36 but Are Differently Regulated Than Gap Junctions in AII Amacrine Cells

inferredcites →https://doi.org/10.7554/elife.20041openalex-snapshot

Connectivity map of bipolar cells and photoreceptors in the mouse retina

inferredcites →https://doi.org/10.7554/elife.42392openalex-snapshot

Retinal direction selectivity in the absence of asymmetric starburst amacrine cell responses

inferredcites →https://doi.org/10.7554/elife.52949openalex-snapshot

The functional organization of excitation and inhibition in the dendrites of mouse direction-selective ganglion cells

inferredcites →https://doi.org/10.7554/elife.81533openalex-snapshot

Spatiotemporal properties of glutamate input support direction selectivity in the dendrites of retinal starburst amacrine cells

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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inferred← citeshttps://doi.org/10.1007/s10633-026-10098-7openalex-snapshot

Anomalous contrast as an adaptive violation of the Talbot-Plateau law

inferred← citeshttps://doi.org/10.1016/j.cell.2024.11.037openalex-snapshot

Configuration of electrical synapses filters sensory information to drive behavioral choices

inferred← citeshttps://doi.org/10.1016/j.celrep.2025.115373openalex-snapshot

A spherical code of retinal orientation selectivity enables decoding in ensembled and retinotopic operation

inferred← citeshttps://doi.org/10.1016/j.cub.2024.02.001openalex-snapshot

Retinal origin of orientation but not direction selective maps in the superior colliculus

inferred← citeshttps://doi.org/10.1016/j.cub.2024.11.023openalex-snapshot

Layer-specific anatomical and physiological features of the retina’s neurovascular unit

inferred← citeshttps://doi.org/10.1016/j.inffus.2024.102758openalex-snapshot

Alignable kernel network

inferred← citeshttps://doi.org/10.1016/j.isci.2026.116842openalex-snapshot

Intrinsic electrical diversity of PV+ retinal ganglion cells

inferred← citeshttps://doi.org/10.1016/j.neuron.2025.12.042openalex-snapshot

A hierarchical electrical synaptic circuit mechanism for integrative parallel visual processing in the retina

inferred← citeshttps://doi.org/10.1016/j.neuroscience.2025.06.044openalex-snapshot

Inhibition of ER stress mitigates hypobaric hypoxia-induced retinal damage: a simulated high-altitude study

inferred← citeshttps://doi.org/10.1038/s41467-024-46348-yopenalex-snapshot

Distributed feature representations of natural stimuli across parallel retinal pathways

inferred← citeshttps://doi.org/10.1038/s41467-026-70288-4openalex-snapshot

Machine learning discovers numerous new computational principles supporting elementary motion detection

inferred← citeshttps://doi.org/10.1073/pnas.2411130121openalex-snapshot

Compartmentalized pooling generates orientation selectivity in wide-field amacrine cells

inferred← citeshttps://doi.org/10.1073/pnas.2415223122openalex-snapshot

Retinal ganglion cells encode the direction of motion outside their classical receptive field

inferred← citeshttps://doi.org/10.1101/2023.08.01.551556openalex-snapshot

Specific Configurations of Electrical Synapses Filter Sensory Information to Drive Choices in Behavior

inferred← citeshttps://doi.org/10.1101/2023.08.02.551732openalex-snapshot

Heterogeneous presynaptic receptive fields contribute to directional tuning in starburst amacrine cells

inferred← citeshttps://doi.org/10.1101/2023.12.28.573580openalex-snapshot

Molecular identification of wide-field amacrine cells in mouse retina that encode stimulus orientation

inferred← citeshttps://doi.org/10.1146/annurev-vision-102122-110414openalex-snapshot

Retinal Connectomics: A Review

inferred← citeshttps://doi.org/10.1152/jn.00472.2025openalex-snapshot

Long-distance object motion evokes direction selectivity in retinal neurons through nicotinic receptors in bipolar cells

inferred← citeshttps://doi.org/10.1523/jneurosci.0910-23.2023openalex-snapshot

Neural Circuits Underlying Multifeature Extraction in the Retina

inferred← citeshttps://doi.org/10.3389/fnins.2026.1816252openalex-snapshot

Unraveling the role of asymmetric excitatory and inhibitory synaptic inputs to retinal ganglion cell direction selectivity

inferred← citeshttps://doi.org/10.3389/fopht.2023.1168548openalex-snapshot

New insights into retinal circuits through EM connectomics: what we have learnt and what remains to be learned

inferred← citeshttps://doi.org/10.7554/elife.90456openalex-snapshot

Heterogeneous presynaptic receptive fields contribute to directional tuning in starburst amacrine cells

inferred← citeshttps://doi.org/10.7554/elife.90456.1openalex-snapshot

Heterogeneous presynaptic receptive fields contribute to directional tuning in starburst amacrine cells

inferred← citeshttps://doi.org/10.7554/elife.90456.1.sa0openalex-snapshot

Reviewer #3 (Public Review): Heterogeneous presynaptic receptive fields contribute to directional tuning in starburst amacrine cells

inferred← citeshttps://doi.org/10.7554/elife.90456.1.sa3openalex-snapshot

eLife Assessment: Heterogeneous presynaptic receptive fields contribute to directional tuning in starburst amacrine cells

inferred← citeshttps://doi.org/10.7554/elife.90456.2openalex-snapshot

Heterogeneous presynaptic receptive fields contribute to directional tuning in starburst amacrine cells

inferred← citeshttps://doi.org/10.7554/elife.90456.3openalex-snapshot

Heterogeneous presynaptic receptive fields contribute to directional tuning in starburst amacrine cells

inferred← citeshttps://doi.org/10.7554/elife.94985openalex-snapshot

Molecular identification of wide-field amacrine cells in mouse retina that encode stimulus orientation

inferred← citeshttps://doi.org/10.7554/elife.94985.1openalex-snapshot

Molecular identification of wide-field amacrine cells in mouse retina that encode stimulus orientation

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