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How Diverse Retinal Functions Arise from Feedback at the First Visual Synapse
- Source :
- Neuron, Neuron, Elsevier, 2018, 99 (1), pp.117-134.e11. ⟨10.1016/j.neuron.2018.06.001⟩
- Publication Year :
- 2018
- Publisher :
- Elsevier BV, 2018.
-
Abstract
- International audience; Many brain regions contain local interneurons of distinct types. How does an interneuron type contribute to the input-output transformations of a given brain region? We addressed this question in the mouse retina by chemogenetically perturbing horizontal cells, an interneuron type providing feedback at the first visual synapse, while monitoring the light-driven spiking activity in thousands of ganglion cells, the retinal output neurons. We uncovered six reversible perturbation-induced effects in the response dynamics and response range of ganglion cells. The effects were enhancing or suppressive, occurred in different response epochs, and depended on the ganglion cell type. A computational model of the retinal circuitry reproduced all perturbation-induced effects and led us to assign specific functions to horizontal cells with respect to different ganglion cell types. Our combined experimental and theoretical work reveals how a single interneuron type can differentially shape the dynamical properties of distinct output channels of a brain region.
- Subjects :
- Retinal Ganglion Cells
0301 basic medicine
Retinal Bipolar Cells
Cell type
Interneuron
[SDV]Life Sciences [q-bio]
Models, Neurological
Retinal Horizontal Cells
Biology
Feedback
Synapse
Mice
03 medical and health sciences
chemistry.chemical_compound
Interneurons
medicine
Animals
Vision, Ocular
Retina
General Neuroscience
Retinal
Ganglion
Brain region
030104 developmental biology
medicine.anatomical_structure
chemistry
Mouse Retina
Synapses
Calcium
Neuroscience
Photoreceptor Cells, Vertebrate
Subjects
Details
- ISSN :
- 08966273
- Volume :
- 99
- Database :
- OpenAIRE
- Journal :
- Neuron
- Accession number :
- edsair.doi.dedup.....68fe40f6bf5f08eb24083cfec3df19ea
- Full Text :
- https://doi.org/10.1016/j.neuron.2018.06.001