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Simple integration of fast excitation and offset, delayed inhibition computes directional selectivity in Drosophila

A neuron that extracts directionally selective motion information from upstream signals lacking this selectivity must compare visual responses from spatially offset inputs. Distinguishing among prevailing algorithmic models for this computation requires measuring fast neuronal activity and inhibitio...

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Detalles Bibliográficos
Autores principales: Gruntman, Eyal, Romani, Sandro, Reiser, Michael B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5967973/
https://www.ncbi.nlm.nih.gov/pubmed/29311742
http://dx.doi.org/10.1038/s41593-017-0046-4
Descripción
Sumario:A neuron that extracts directionally selective motion information from upstream signals lacking this selectivity must compare visual responses from spatially offset inputs. Distinguishing among prevailing algorithmic models for this computation requires measuring fast neuronal activity and inhibition. In the Drosophila visual system, a 4(th)-order neuron—T4—is the first cell type in the ON pathway to exhibit directionally selective signals. Here we use in-vivo whole cell recordings of T4 to show that directional selectivity originates from simple integration of spatially offset fast excitatory and slow inhibitory inputs, resulting in a suppression of responses to the non-preferred motion direction. We constructed a passive, conductance-based model of a T4 cell that accurately predicts the neuron’s response to moving stimuli. These results connect the known circuit anatomy of the motion pathway to the algorithmic mechanism by which the direction of motion is computed.