| Literature DB >> 28514655 |
Tahnbee Kim1, Daniel Kerschensteiner2.
Abstract
Object motion sensitive (OMS) W3-retinal ganglion cells (W3-RGCs) in mice respond to local movements in a visual scene but remain silent during self-generated global image motion. The excitatory inputs that drive responses of W3-RGCs to local motion were recently characterized, but which inhibitory neurons suppress W3-RGCs' responses to global motion, how these neurons encode motion information, and how their connections are organized along the excitatory circuit axis remains unknown. Here, we find that a genetically identified amacrine cell (AC) type, TH2-AC, exhibits fast responses to global motion and slow responses to local motion. Optogenetic stimulation shows that TH2-ACs provide strong GABAA receptor-mediated input to W3-RGCs but only weak input to upstream excitatory neurons. Cell-type-specific silencing reveals that temporally coded inhibition from TH2-ACs cancels W3-RGC spike responses to global but not local motion stimuli and, thus, controls the feature selectivity of OMS signals sent to the brain.Entities:
Keywords: amacrine cell; feature selectivity; object motion; retina; surround inhibition; temporal coding
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Year: 2017 PMID: 28514655 PMCID: PMC5501491 DOI: 10.1016/j.celrep.2017.04.060
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423