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A visual circuit uses complementary mechanisms to support transient and sustained pupil constriction

Rapid and stable control of pupil size in response to light is critical for vision, but the neural coding mechanisms remain unclear. Here, we investigated the neural basis of pupil control by monitoring pupil size across time while manipulating each photoreceptor input or neurotransmitter output of...

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Autores principales: Keenan, William Thomas, Rupp, Alan C, Ross, Rachel A, Somasundaram, Preethi, Hiriyanna, Suja, Wu, Zhijian, Badea, Tudor C, Robinson, Phyllis R, Lowell, Bradford B, Hattar, Samer S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5079752/
https://www.ncbi.nlm.nih.gov/pubmed/27669145
http://dx.doi.org/10.7554/eLife.15392
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author Keenan, William Thomas
Rupp, Alan C
Ross, Rachel A
Somasundaram, Preethi
Hiriyanna, Suja
Wu, Zhijian
Badea, Tudor C
Robinson, Phyllis R
Lowell, Bradford B
Hattar, Samer S
author_facet Keenan, William Thomas
Rupp, Alan C
Ross, Rachel A
Somasundaram, Preethi
Hiriyanna, Suja
Wu, Zhijian
Badea, Tudor C
Robinson, Phyllis R
Lowell, Bradford B
Hattar, Samer S
author_sort Keenan, William Thomas
collection PubMed
description Rapid and stable control of pupil size in response to light is critical for vision, but the neural coding mechanisms remain unclear. Here, we investigated the neural basis of pupil control by monitoring pupil size across time while manipulating each photoreceptor input or neurotransmitter output of intrinsically photosensitive retinal ganglion cells (ipRGCs), a critical relay in the control of pupil size. We show that transient and sustained pupil responses are mediated by distinct photoreceptors and neurotransmitters. Transient responses utilize input from rod photoreceptors and output by the classical neurotransmitter glutamate, but adapt within minutes. In contrast, sustained responses are dominated by non-conventional signaling mechanisms: melanopsin phototransduction in ipRGCs and output by the neuropeptide PACAP, which provide stable pupil maintenance across the day. These results highlight a temporal switch in the coding mechanisms of a neural circuit to support proper behavioral dynamics. DOI: http://dx.doi.org/10.7554/eLife.15392.001
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spelling pubmed-50797522016-10-26 A visual circuit uses complementary mechanisms to support transient and sustained pupil constriction Keenan, William Thomas Rupp, Alan C Ross, Rachel A Somasundaram, Preethi Hiriyanna, Suja Wu, Zhijian Badea, Tudor C Robinson, Phyllis R Lowell, Bradford B Hattar, Samer S eLife Neuroscience Rapid and stable control of pupil size in response to light is critical for vision, but the neural coding mechanisms remain unclear. Here, we investigated the neural basis of pupil control by monitoring pupil size across time while manipulating each photoreceptor input or neurotransmitter output of intrinsically photosensitive retinal ganglion cells (ipRGCs), a critical relay in the control of pupil size. We show that transient and sustained pupil responses are mediated by distinct photoreceptors and neurotransmitters. Transient responses utilize input from rod photoreceptors and output by the classical neurotransmitter glutamate, but adapt within minutes. In contrast, sustained responses are dominated by non-conventional signaling mechanisms: melanopsin phototransduction in ipRGCs and output by the neuropeptide PACAP, which provide stable pupil maintenance across the day. These results highlight a temporal switch in the coding mechanisms of a neural circuit to support proper behavioral dynamics. DOI: http://dx.doi.org/10.7554/eLife.15392.001 eLife Sciences Publications, Ltd 2016-09-26 /pmc/articles/PMC5079752/ /pubmed/27669145 http://dx.doi.org/10.7554/eLife.15392 Text en http://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication (http://creativecommons.org/publicdomain/zero/1.0/) .
spellingShingle Neuroscience
Keenan, William Thomas
Rupp, Alan C
Ross, Rachel A
Somasundaram, Preethi
Hiriyanna, Suja
Wu, Zhijian
Badea, Tudor C
Robinson, Phyllis R
Lowell, Bradford B
Hattar, Samer S
A visual circuit uses complementary mechanisms to support transient and sustained pupil constriction
title A visual circuit uses complementary mechanisms to support transient and sustained pupil constriction
title_full A visual circuit uses complementary mechanisms to support transient and sustained pupil constriction
title_fullStr A visual circuit uses complementary mechanisms to support transient and sustained pupil constriction
title_full_unstemmed A visual circuit uses complementary mechanisms to support transient and sustained pupil constriction
title_short A visual circuit uses complementary mechanisms to support transient and sustained pupil constriction
title_sort visual circuit uses complementary mechanisms to support transient and sustained pupil constriction
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5079752/
https://www.ncbi.nlm.nih.gov/pubmed/27669145
http://dx.doi.org/10.7554/eLife.15392
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