Spatially displaced excitation contributes to the encoding of interrupted motion by a retinal direction-selective circuit.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 34096504.
- Also identified by DOI 10.7554/eLife.68181 and PMC identifier 8211448.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Spatially distributed excitation and inhibition collectively shape a visual neuron's receptive field (RF) properties. In the direction-selective circuit of the mammalian retina, the role of strong null-direction inhibition of On-Off direction-selective ganglion cells (On-Off DSGCs) on their direction selectivity is well-studied. However, how excitatory inputs influence the On-Off DSGC's visual response is underexplored. Here, we report that On-Off DSGCs have a spatially displaced glutamatergic receptive field along their horizontal preferred-null motion axes. This displaced receptive field contributes to DSGC null-direction spiking during interrupted motion trajectories. Theoretical analyses indicate that population responses during interrupted motion may help populations of On-Off DSGCs signal the spatial location of moving objects in complex, naturalistic visual environments. Our study highlights that the direction-selective circuit exploits separate sets of mechanisms under different stimulus conditions, and these mechanisms may help encode multiple visual features.
Medical subject headings
- Animals
- Calcium Signaling
- Evoked Potentials, Visual
- Excitatory Postsynaptic Potentials
- Female
- Glutamic Acid
- Glutamic Acid/metabolism
- Male
- Mice, 129 Strain
- Mice, Inbred C57BL
- Mice, Transgenic
- Models, Neurological
- Motion Perception
- Photic Stimulation
- Retinal Ganglion Cells
- Retinal Ganglion Cells/metabolism
- Retinal Ganglion Cells/physiology
- Synaptic Transmission
- Time Factors
- Visual Fields
- Mice