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Melanopsin-Driven Light Adaptation in Mouse Vision
BACKGROUND: In bright light, mammals use a distinct photopigment (melanopsin) to measure irradiance for centrally mediated responses such as circadian entrainment. We aimed to determine whether the information generated by melanopsin is also used by the visual system as a signal for light adaptation...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4228053/ https://www.ncbi.nlm.nih.gov/pubmed/25308073 http://dx.doi.org/10.1016/j.cub.2014.09.015 |
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author | Allen, Annette E. Storchi, Riccardo Martial, Franck P. Petersen, Rasmus S. Montemurro, Marcelo A. Brown, Timothy M. Lucas, Robert J. |
author_facet | Allen, Annette E. Storchi, Riccardo Martial, Franck P. Petersen, Rasmus S. Montemurro, Marcelo A. Brown, Timothy M. Lucas, Robert J. |
author_sort | Allen, Annette E. |
collection | PubMed |
description | BACKGROUND: In bright light, mammals use a distinct photopigment (melanopsin) to measure irradiance for centrally mediated responses such as circadian entrainment. We aimed to determine whether the information generated by melanopsin is also used by the visual system as a signal for light adaptation. To this end, we compared retinal and thalamic responses to a range of artificial and natural visual stimuli presented using spectral compositions that either approximate the mouse’s experience of natural daylight (“daylight”) or are selectively depleted of wavelengths to which melanopsin is most sensitive (“mel-low”). RESULTS: We found reproducible and reversible changes in the flash electroretinogram between daylight and mel-low. Simultaneous recording in the dorsal lateral geniculate nucleus (dLGN) revealed that these reflect changes in feature selectivity of visual circuits in both temporal and spatial dimensions. A substantial fraction of units preferred finer spatial patterns in the daylight condition, while the population of direction-sensitive units became tuned to faster motion. The dLGN contained a richer, more reliable encoding of natural scenes in the daylight condition. These effects were absent in mice lacking melanopsin. CONCLUSIONS: The feature selectivity of many neurons in the mouse dLGN is adjusted according to a melanopsin-dependent measure of environmental brightness. These changes originate, at least in part, within the retina. Melanopsin performs a role analogous to a photographer’s light meter, providing an independent measure of irradiance that determines optimal setting for visual circuits. |
format | Online Article Text |
id | pubmed-4228053 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-42280532014-11-13 Melanopsin-Driven Light Adaptation in Mouse Vision Allen, Annette E. Storchi, Riccardo Martial, Franck P. Petersen, Rasmus S. Montemurro, Marcelo A. Brown, Timothy M. Lucas, Robert J. Curr Biol Article BACKGROUND: In bright light, mammals use a distinct photopigment (melanopsin) to measure irradiance for centrally mediated responses such as circadian entrainment. We aimed to determine whether the information generated by melanopsin is also used by the visual system as a signal for light adaptation. To this end, we compared retinal and thalamic responses to a range of artificial and natural visual stimuli presented using spectral compositions that either approximate the mouse’s experience of natural daylight (“daylight”) or are selectively depleted of wavelengths to which melanopsin is most sensitive (“mel-low”). RESULTS: We found reproducible and reversible changes in the flash electroretinogram between daylight and mel-low. Simultaneous recording in the dorsal lateral geniculate nucleus (dLGN) revealed that these reflect changes in feature selectivity of visual circuits in both temporal and spatial dimensions. A substantial fraction of units preferred finer spatial patterns in the daylight condition, while the population of direction-sensitive units became tuned to faster motion. The dLGN contained a richer, more reliable encoding of natural scenes in the daylight condition. These effects were absent in mice lacking melanopsin. CONCLUSIONS: The feature selectivity of many neurons in the mouse dLGN is adjusted according to a melanopsin-dependent measure of environmental brightness. These changes originate, at least in part, within the retina. Melanopsin performs a role analogous to a photographer’s light meter, providing an independent measure of irradiance that determines optimal setting for visual circuits. Cell Press 2014-11-03 /pmc/articles/PMC4228053/ /pubmed/25308073 http://dx.doi.org/10.1016/j.cub.2014.09.015 Text en © 2014 The Authors https://creativecommons.org/licenses/by/3.0/This work is licensed under a Creative Commons Attribution 3.0 Unported License (https://creativecommons.org/licenses/by/3.0/) . |
spellingShingle | Article Allen, Annette E. Storchi, Riccardo Martial, Franck P. Petersen, Rasmus S. Montemurro, Marcelo A. Brown, Timothy M. Lucas, Robert J. Melanopsin-Driven Light Adaptation in Mouse Vision |
title | Melanopsin-Driven Light Adaptation in Mouse Vision |
title_full | Melanopsin-Driven Light Adaptation in Mouse Vision |
title_fullStr | Melanopsin-Driven Light Adaptation in Mouse Vision |
title_full_unstemmed | Melanopsin-Driven Light Adaptation in Mouse Vision |
title_short | Melanopsin-Driven Light Adaptation in Mouse Vision |
title_sort | melanopsin-driven light adaptation in mouse vision |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4228053/ https://www.ncbi.nlm.nih.gov/pubmed/25308073 http://dx.doi.org/10.1016/j.cub.2014.09.015 |
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