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Distinct Contributions of Rod, Cone, and Melanopsin Photoreceptors to Encoding Irradiance

Photoreceptive, melanopsin-expressing retinal ganglion cells (mRGCs) encode ambient light (irradiance) for the circadian clock, the pupillomotor system, and other influential behavioral/physiological responses. mRGCs are activated both by their intrinsic phototransduction cascade and by the rods and...

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Autores principales: Lall, Gurprit S., Revell, Victoria L., Momiji, Hiroshi, Al Enezi, Jazi, Altimus, Cara M., Güler, Ali D., Aguilar, Carlos, Cameron, Morven A., Allender, Susan, Hankins, Mark W., Lucas, Robert J.
Formato: Texto
Lenguaje:English
Publicado: Cell Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2875410/
https://www.ncbi.nlm.nih.gov/pubmed/20471354
http://dx.doi.org/10.1016/j.neuron.2010.04.037
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author Lall, Gurprit S.
Revell, Victoria L.
Momiji, Hiroshi
Al Enezi, Jazi
Altimus, Cara M.
Güler, Ali D.
Aguilar, Carlos
Cameron, Morven A.
Allender, Susan
Hankins, Mark W.
Lucas, Robert J.
author_facet Lall, Gurprit S.
Revell, Victoria L.
Momiji, Hiroshi
Al Enezi, Jazi
Altimus, Cara M.
Güler, Ali D.
Aguilar, Carlos
Cameron, Morven A.
Allender, Susan
Hankins, Mark W.
Lucas, Robert J.
author_sort Lall, Gurprit S.
collection PubMed
description Photoreceptive, melanopsin-expressing retinal ganglion cells (mRGCs) encode ambient light (irradiance) for the circadian clock, the pupillomotor system, and other influential behavioral/physiological responses. mRGCs are activated both by their intrinsic phototransduction cascade and by the rods and cones. However, the individual contribution of each photoreceptor class to irradiance responses remains unclear. We address this deficit using mice expressing human red cone opsin, in which rod-, cone-, and melanopsin-dependent responses can be identified by their distinct spectral sensitivity. Our data reveal an unexpectedly important role for rods. These photoreceptors define circadian responses at very dim “scotopic” light levels but also at irradiances at which pattern vision relies heavily on cones. By contrast, cone input to irradiance responses dissipates following light adaptation to the extent that these receptors make a very limited contribution to circadian and pupillary light responses under these conditions. Our data provide new insight into retinal circuitry upstream of mRGCs and optimal stimuli for eliciting irradiance responses.
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spelling pubmed-28754102010-06-10 Distinct Contributions of Rod, Cone, and Melanopsin Photoreceptors to Encoding Irradiance Lall, Gurprit S. Revell, Victoria L. Momiji, Hiroshi Al Enezi, Jazi Altimus, Cara M. Güler, Ali D. Aguilar, Carlos Cameron, Morven A. Allender, Susan Hankins, Mark W. Lucas, Robert J. Neuron Article Photoreceptive, melanopsin-expressing retinal ganglion cells (mRGCs) encode ambient light (irradiance) for the circadian clock, the pupillomotor system, and other influential behavioral/physiological responses. mRGCs are activated both by their intrinsic phototransduction cascade and by the rods and cones. However, the individual contribution of each photoreceptor class to irradiance responses remains unclear. We address this deficit using mice expressing human red cone opsin, in which rod-, cone-, and melanopsin-dependent responses can be identified by their distinct spectral sensitivity. Our data reveal an unexpectedly important role for rods. These photoreceptors define circadian responses at very dim “scotopic” light levels but also at irradiances at which pattern vision relies heavily on cones. By contrast, cone input to irradiance responses dissipates following light adaptation to the extent that these receptors make a very limited contribution to circadian and pupillary light responses under these conditions. Our data provide new insight into retinal circuitry upstream of mRGCs and optimal stimuli for eliciting irradiance responses. Cell Press 2010-05-13 /pmc/articles/PMC2875410/ /pubmed/20471354 http://dx.doi.org/10.1016/j.neuron.2010.04.037 Text en © 2010 ELL & Excerpta Medica. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license
spellingShingle Article
Lall, Gurprit S.
Revell, Victoria L.
Momiji, Hiroshi
Al Enezi, Jazi
Altimus, Cara M.
Güler, Ali D.
Aguilar, Carlos
Cameron, Morven A.
Allender, Susan
Hankins, Mark W.
Lucas, Robert J.
Distinct Contributions of Rod, Cone, and Melanopsin Photoreceptors to Encoding Irradiance
title Distinct Contributions of Rod, Cone, and Melanopsin Photoreceptors to Encoding Irradiance
title_full Distinct Contributions of Rod, Cone, and Melanopsin Photoreceptors to Encoding Irradiance
title_fullStr Distinct Contributions of Rod, Cone, and Melanopsin Photoreceptors to Encoding Irradiance
title_full_unstemmed Distinct Contributions of Rod, Cone, and Melanopsin Photoreceptors to Encoding Irradiance
title_short Distinct Contributions of Rod, Cone, and Melanopsin Photoreceptors to Encoding Irradiance
title_sort distinct contributions of rod, cone, and melanopsin photoreceptors to encoding irradiance
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2875410/
https://www.ncbi.nlm.nih.gov/pubmed/20471354
http://dx.doi.org/10.1016/j.neuron.2010.04.037
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