Cargando…

Columnar neurons support saccadic bar tracking in Drosophila

Tracking visual objects while maintaining stable gaze is complicated by the different computational requirements for figure-ground discrimination, and the distinct behaviors that these computations coordinate. Drosophila melanogaster uses smooth optomotor head and body movements to stabilize gaze, a...

Descripción completa

Detalles Bibliográficos
Autores principales: Frighetto, Giovanni, Frye, Mark A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10115446/
https://www.ncbi.nlm.nih.gov/pubmed/37014060
http://dx.doi.org/10.7554/eLife.83656
_version_ 1785028215670046720
author Frighetto, Giovanni
Frye, Mark A
author_facet Frighetto, Giovanni
Frye, Mark A
author_sort Frighetto, Giovanni
collection PubMed
description Tracking visual objects while maintaining stable gaze is complicated by the different computational requirements for figure-ground discrimination, and the distinct behaviors that these computations coordinate. Drosophila melanogaster uses smooth optomotor head and body movements to stabilize gaze, and impulsive saccades to pursue elongated vertical bars. Directionally selective motion detectors T4 and T5 cells provide inputs to large-field neurons in the lobula plate, which control optomotor gaze stabilization behavior. Here, we hypothesized that an anatomically parallel pathway represented by T3 cells, which provide inputs to the lobula, drives bar tracking body saccades. We combined physiological and behavioral experiments to show that T3 neurons respond omnidirectionally to the same visual stimuli that elicit bar tracking saccades, silencing T3 reduced the frequency of tracking saccades, and optogenetic manipulation of T3 acted on the saccade rate in a push–pull manner. Manipulating T3 did not affect smooth optomotor responses to large-field motion. Our results show that parallel neural pathways coordinate smooth gaze stabilization and saccadic bar tracking behavior during flight.
format Online
Article
Text
id pubmed-10115446
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher eLife Sciences Publications, Ltd
record_format MEDLINE/PubMed
spelling pubmed-101154462023-04-20 Columnar neurons support saccadic bar tracking in Drosophila Frighetto, Giovanni Frye, Mark A eLife Neuroscience Tracking visual objects while maintaining stable gaze is complicated by the different computational requirements for figure-ground discrimination, and the distinct behaviors that these computations coordinate. Drosophila melanogaster uses smooth optomotor head and body movements to stabilize gaze, and impulsive saccades to pursue elongated vertical bars. Directionally selective motion detectors T4 and T5 cells provide inputs to large-field neurons in the lobula plate, which control optomotor gaze stabilization behavior. Here, we hypothesized that an anatomically parallel pathway represented by T3 cells, which provide inputs to the lobula, drives bar tracking body saccades. We combined physiological and behavioral experiments to show that T3 neurons respond omnidirectionally to the same visual stimuli that elicit bar tracking saccades, silencing T3 reduced the frequency of tracking saccades, and optogenetic manipulation of T3 acted on the saccade rate in a push–pull manner. Manipulating T3 did not affect smooth optomotor responses to large-field motion. Our results show that parallel neural pathways coordinate smooth gaze stabilization and saccadic bar tracking behavior during flight. eLife Sciences Publications, Ltd 2023-04-04 /pmc/articles/PMC10115446/ /pubmed/37014060 http://dx.doi.org/10.7554/eLife.83656 Text en © 2023, Frighetto and Frye https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Frighetto, Giovanni
Frye, Mark A
Columnar neurons support saccadic bar tracking in Drosophila
title Columnar neurons support saccadic bar tracking in Drosophila
title_full Columnar neurons support saccadic bar tracking in Drosophila
title_fullStr Columnar neurons support saccadic bar tracking in Drosophila
title_full_unstemmed Columnar neurons support saccadic bar tracking in Drosophila
title_short Columnar neurons support saccadic bar tracking in Drosophila
title_sort columnar neurons support saccadic bar tracking in drosophila
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10115446/
https://www.ncbi.nlm.nih.gov/pubmed/37014060
http://dx.doi.org/10.7554/eLife.83656
work_keys_str_mv AT frighettogiovanni columnarneuronssupportsaccadicbartrackingindrosophila
AT fryemarka columnarneuronssupportsaccadicbartrackingindrosophila