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Neural mechanisms underlying sensitivity to reverse-phi motion in the fly

Optical illusions provide powerful tools for mapping the algorithms and circuits that underlie visual processing, revealing structure through atypical function. Of particular note in the study of motion detection has been the reverse-phi illusion. When contrast reversals accompany discrete movement,...

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Autores principales: Leonhardt, Aljoscha, Meier, Matthias, Serbe, Etienne, Eichner, Hubert, Borst, Alexander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5737883/
https://www.ncbi.nlm.nih.gov/pubmed/29261684
http://dx.doi.org/10.1371/journal.pone.0189019
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author Leonhardt, Aljoscha
Meier, Matthias
Serbe, Etienne
Eichner, Hubert
Borst, Alexander
author_facet Leonhardt, Aljoscha
Meier, Matthias
Serbe, Etienne
Eichner, Hubert
Borst, Alexander
author_sort Leonhardt, Aljoscha
collection PubMed
description Optical illusions provide powerful tools for mapping the algorithms and circuits that underlie visual processing, revealing structure through atypical function. Of particular note in the study of motion detection has been the reverse-phi illusion. When contrast reversals accompany discrete movement, detected direction tends to invert. This occurs across a wide range of organisms, spanning humans and invertebrates. Here, we map an algorithmic account of the phenomenon onto neural circuitry in the fruit fly Drosophila melanogaster. Through targeted silencing experiments in tethered walking flies as well as electrophysiology and calcium imaging, we demonstrate that ON- or OFF-selective local motion detector cells T4 and T5 are sensitive to certain interactions between ON and OFF. A biologically plausible detector model accounts for subtle features of this particular form of illusory motion reversal, like the re-inversion of turning responses occurring at extreme stimulus velocities. In light of comparable circuit architecture in the mammalian retina, we suggest that similar mechanisms may apply even to human psychophysics.
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spelling pubmed-57378832017-12-29 Neural mechanisms underlying sensitivity to reverse-phi motion in the fly Leonhardt, Aljoscha Meier, Matthias Serbe, Etienne Eichner, Hubert Borst, Alexander PLoS One Research Article Optical illusions provide powerful tools for mapping the algorithms and circuits that underlie visual processing, revealing structure through atypical function. Of particular note in the study of motion detection has been the reverse-phi illusion. When contrast reversals accompany discrete movement, detected direction tends to invert. This occurs across a wide range of organisms, spanning humans and invertebrates. Here, we map an algorithmic account of the phenomenon onto neural circuitry in the fruit fly Drosophila melanogaster. Through targeted silencing experiments in tethered walking flies as well as electrophysiology and calcium imaging, we demonstrate that ON- or OFF-selective local motion detector cells T4 and T5 are sensitive to certain interactions between ON and OFF. A biologically plausible detector model accounts for subtle features of this particular form of illusory motion reversal, like the re-inversion of turning responses occurring at extreme stimulus velocities. In light of comparable circuit architecture in the mammalian retina, we suggest that similar mechanisms may apply even to human psychophysics. Public Library of Science 2017-12-20 /pmc/articles/PMC5737883/ /pubmed/29261684 http://dx.doi.org/10.1371/journal.pone.0189019 Text en © 2017 Leonhardt et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Leonhardt, Aljoscha
Meier, Matthias
Serbe, Etienne
Eichner, Hubert
Borst, Alexander
Neural mechanisms underlying sensitivity to reverse-phi motion in the fly
title Neural mechanisms underlying sensitivity to reverse-phi motion in the fly
title_full Neural mechanisms underlying sensitivity to reverse-phi motion in the fly
title_fullStr Neural mechanisms underlying sensitivity to reverse-phi motion in the fly
title_full_unstemmed Neural mechanisms underlying sensitivity to reverse-phi motion in the fly
title_short Neural mechanisms underlying sensitivity to reverse-phi motion in the fly
title_sort neural mechanisms underlying sensitivity to reverse-phi motion in the fly
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5737883/
https://www.ncbi.nlm.nih.gov/pubmed/29261684
http://dx.doi.org/10.1371/journal.pone.0189019
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