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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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American Association for the Advancement of Science
2020
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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. |
format | Online Article Text |
id | pubmed-7164931 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
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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