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Hawkmoth lamina monopolar cells act as dynamic spatial filters to optimize vision at different light levels

How neural form and function are connected is a central question of neuroscience. One prominent functional hypothesis, from the beginnings of neuroanatomical study, states that laterally extending dendrites of insect lamina monopolar cells (LMCs) spatially integrate visual information. We provide th...

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Autores principales: Stöckl, Anna Lisa, O’Carroll, David Charles, Warrant, Eric James
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7164931/
https://www.ncbi.nlm.nih.gov/pubmed/32494622
http://dx.doi.org/10.1126/sciadv.aaz8645
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author Stöckl, Anna Lisa
O’Carroll, David Charles
Warrant, Eric James
author_facet Stöckl, Anna Lisa
O’Carroll, David Charles
Warrant, Eric James
author_sort Stöckl, Anna Lisa
collection PubMed
description How neural form and function are connected is a central question of neuroscience. One prominent functional hypothesis, from the beginnings of neuroanatomical study, states that laterally extending dendrites of insect lamina monopolar cells (LMCs) spatially integrate visual information. We provide the first direct functional evidence for this hypothesis using intracellular recordings from type II LMCs in the hawkmoth Macroglossum stellatarum. We show that their spatial receptive fields broaden with decreasing light intensities, thus trading spatial resolution for higher sensitivity. These dynamic changes in LMC spatial properties can be explained by the density and lateral extent of their dendritic arborizations. Our results thus provide the first physiological evidence for a century-old hypothesis, directly correlating physiological response properties with distinctive dendritic morphology.
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spelling pubmed-71649312020-06-02 Hawkmoth lamina monopolar cells act as dynamic spatial filters to optimize vision at different light levels Stöckl, Anna Lisa O’Carroll, David Charles Warrant, Eric James Sci Adv Research Articles How neural form and function are connected is a central question of neuroscience. One prominent functional hypothesis, from the beginnings of neuroanatomical study, states that laterally extending dendrites of insect lamina monopolar cells (LMCs) spatially integrate visual information. We provide the first direct functional evidence for this hypothesis using intracellular recordings from type II LMCs in the hawkmoth Macroglossum stellatarum. We show that their spatial receptive fields broaden with decreasing light intensities, thus trading spatial resolution for higher sensitivity. These dynamic changes in LMC spatial properties can be explained by the density and lateral extent of their dendritic arborizations. Our results thus provide the first physiological evidence for a century-old hypothesis, directly correlating physiological response properties with distinctive dendritic morphology. American Association for the Advancement of Science 2020-04-17 /pmc/articles/PMC7164931/ /pubmed/32494622 http://dx.doi.org/10.1126/sciadv.aaz8645 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Stöckl, Anna Lisa
O’Carroll, David Charles
Warrant, Eric James
Hawkmoth lamina monopolar cells act as dynamic spatial filters to optimize vision at different light levels
title Hawkmoth lamina monopolar cells act as dynamic spatial filters to optimize vision at different light levels
title_full Hawkmoth lamina monopolar cells act as dynamic spatial filters to optimize vision at different light levels
title_fullStr Hawkmoth lamina monopolar cells act as dynamic spatial filters to optimize vision at different light levels
title_full_unstemmed Hawkmoth lamina monopolar cells act as dynamic spatial filters to optimize vision at different light levels
title_short Hawkmoth lamina monopolar cells act as dynamic spatial filters to optimize vision at different light levels
title_sort hawkmoth lamina monopolar cells act as dynamic spatial filters to optimize vision at different light levels
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7164931/
https://www.ncbi.nlm.nih.gov/pubmed/32494622
http://dx.doi.org/10.1126/sciadv.aaz8645
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