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Circadian and light-driven regulation of rod dark adaptation

Continuous visual perception and the dark adaptation of vertebrate photoreceptors after bright light exposure require recycling of their visual chromophore through a series of reactions in the retinal pigmented epithelium (RPE visual cycle). Light-driven chromophore consumption by photoreceptors is...

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Autores principales: Xue, Yunlu, Shen, Susan Q., Corbo, Joseph C., Kefalov, Vladimir J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4667277/
https://www.ncbi.nlm.nih.gov/pubmed/26626567
http://dx.doi.org/10.1038/srep17616
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author Xue, Yunlu
Shen, Susan Q.
Corbo, Joseph C.
Kefalov, Vladimir J.
author_facet Xue, Yunlu
Shen, Susan Q.
Corbo, Joseph C.
Kefalov, Vladimir J.
author_sort Xue, Yunlu
collection PubMed
description Continuous visual perception and the dark adaptation of vertebrate photoreceptors after bright light exposure require recycling of their visual chromophore through a series of reactions in the retinal pigmented epithelium (RPE visual cycle). Light-driven chromophore consumption by photoreceptors is greater in daytime vs. nighttime, suggesting that correspondingly higher activity of the visual cycle may be required. However, as rod photoreceptors are saturated in bright light, the continuous turnover of their chromophore by the visual cycle throughout the day would not contribute to vision. Whether the recycling of chromophore that drives rod dark adaptation is regulated by the circadian clock and light exposure is unknown. Here, we demonstrate that mouse rod dark adaptation is slower during the day or after light pre-exposure. This surprising daytime suppression of the RPE visual cycle was accompanied by light-driven reduction in expression of Rpe65, a key enzyme of the RPE visual cycle. Notably, only rods in melatonin-proficient mice were affected by this daily visual cycle modulation. Our results demonstrate that the circadian clock and light exposure regulate the recycling of chromophore in the RPE visual cycle. This daily melatonin-driven modulation of rod dark adaptation could potentially protect the retina from light-induced damage during the day.
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spelling pubmed-46672772015-12-08 Circadian and light-driven regulation of rod dark adaptation Xue, Yunlu Shen, Susan Q. Corbo, Joseph C. Kefalov, Vladimir J. Sci Rep Article Continuous visual perception and the dark adaptation of vertebrate photoreceptors after bright light exposure require recycling of their visual chromophore through a series of reactions in the retinal pigmented epithelium (RPE visual cycle). Light-driven chromophore consumption by photoreceptors is greater in daytime vs. nighttime, suggesting that correspondingly higher activity of the visual cycle may be required. However, as rod photoreceptors are saturated in bright light, the continuous turnover of their chromophore by the visual cycle throughout the day would not contribute to vision. Whether the recycling of chromophore that drives rod dark adaptation is regulated by the circadian clock and light exposure is unknown. Here, we demonstrate that mouse rod dark adaptation is slower during the day or after light pre-exposure. This surprising daytime suppression of the RPE visual cycle was accompanied by light-driven reduction in expression of Rpe65, a key enzyme of the RPE visual cycle. Notably, only rods in melatonin-proficient mice were affected by this daily visual cycle modulation. Our results demonstrate that the circadian clock and light exposure regulate the recycling of chromophore in the RPE visual cycle. This daily melatonin-driven modulation of rod dark adaptation could potentially protect the retina from light-induced damage during the day. Nature Publishing Group 2015-12-02 /pmc/articles/PMC4667277/ /pubmed/26626567 http://dx.doi.org/10.1038/srep17616 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Xue, Yunlu
Shen, Susan Q.
Corbo, Joseph C.
Kefalov, Vladimir J.
Circadian and light-driven regulation of rod dark adaptation
title Circadian and light-driven regulation of rod dark adaptation
title_full Circadian and light-driven regulation of rod dark adaptation
title_fullStr Circadian and light-driven regulation of rod dark adaptation
title_full_unstemmed Circadian and light-driven regulation of rod dark adaptation
title_short Circadian and light-driven regulation of rod dark adaptation
title_sort circadian and light-driven regulation of rod dark adaptation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4667277/
https://www.ncbi.nlm.nih.gov/pubmed/26626567
http://dx.doi.org/10.1038/srep17616
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