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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2018
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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 |
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author | Gruntman, Eyal Romani, Sandro Reiser, Michael B. |
author_facet | Gruntman, Eyal Romani, Sandro Reiser, Michael B. |
author_sort | Gruntman, Eyal |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-5967973 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
record_format | MEDLINE/PubMed |
spelling | pubmed-59679732018-07-08 Simple integration of fast excitation and offset, delayed inhibition computes directional selectivity in Drosophila Gruntman, Eyal Romani, Sandro Reiser, Michael B. Nat Neurosci Article 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. 2018-01-08 2018-02 /pmc/articles/PMC5967973/ /pubmed/29311742 http://dx.doi.org/10.1038/s41593-017-0046-4 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Gruntman, Eyal Romani, Sandro Reiser, Michael B. Simple integration of fast excitation and offset, delayed inhibition computes directional selectivity in Drosophila |
title | Simple integration of fast excitation and offset, delayed inhibition
computes directional selectivity in Drosophila |
title_full | Simple integration of fast excitation and offset, delayed inhibition
computes directional selectivity in Drosophila |
title_fullStr | Simple integration of fast excitation and offset, delayed inhibition
computes directional selectivity in Drosophila |
title_full_unstemmed | Simple integration of fast excitation and offset, delayed inhibition
computes directional selectivity in Drosophila |
title_short | Simple integration of fast excitation and offset, delayed inhibition
computes directional selectivity in Drosophila |
title_sort | simple integration of fast excitation and offset, delayed inhibition
computes directional selectivity in drosophila |
topic | Article |
url | 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 |
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