Cargando…
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...
Autores principales: | , , , , , , , , , |
---|---|
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 |
_version_ | 1782462597246746624 |
---|---|
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 |
format | Online Article Text |
id | pubmed-5079752 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT keenanwilliamthomas avisualcircuitusescomplementarymechanismstosupporttransientandsustainedpupilconstriction AT ruppalanc avisualcircuitusescomplementarymechanismstosupporttransientandsustainedpupilconstriction AT rossrachela avisualcircuitusescomplementarymechanismstosupporttransientandsustainedpupilconstriction AT somasundarampreethi avisualcircuitusescomplementarymechanismstosupporttransientandsustainedpupilconstriction AT hiriyannasuja avisualcircuitusescomplementarymechanismstosupporttransientandsustainedpupilconstriction AT wuzhijian avisualcircuitusescomplementarymechanismstosupporttransientandsustainedpupilconstriction AT badeatudorc avisualcircuitusescomplementarymechanismstosupporttransientandsustainedpupilconstriction AT robinsonphyllisr avisualcircuitusescomplementarymechanismstosupporttransientandsustainedpupilconstriction AT lowellbradfordb avisualcircuitusescomplementarymechanismstosupporttransientandsustainedpupilconstriction AT hattarsamers avisualcircuitusescomplementarymechanismstosupporttransientandsustainedpupilconstriction AT keenanwilliamthomas visualcircuitusescomplementarymechanismstosupporttransientandsustainedpupilconstriction AT ruppalanc visualcircuitusescomplementarymechanismstosupporttransientandsustainedpupilconstriction AT rossrachela visualcircuitusescomplementarymechanismstosupporttransientandsustainedpupilconstriction AT somasundarampreethi visualcircuitusescomplementarymechanismstosupporttransientandsustainedpupilconstriction AT hiriyannasuja visualcircuitusescomplementarymechanismstosupporttransientandsustainedpupilconstriction AT wuzhijian visualcircuitusescomplementarymechanismstosupporttransientandsustainedpupilconstriction AT badeatudorc visualcircuitusescomplementarymechanismstosupporttransientandsustainedpupilconstriction AT robinsonphyllisr visualcircuitusescomplementarymechanismstosupporttransientandsustainedpupilconstriction AT lowellbradfordb visualcircuitusescomplementarymechanismstosupporttransientandsustainedpupilconstriction AT hattarsamers visualcircuitusescomplementarymechanismstosupporttransientandsustainedpupilconstriction |