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Rods contribute to the light-induced phase shift of the retinal clock in mammals
While rods, cones, and intrinsically photosensitive melanopsin-containing ganglion cells (ipRGCs) all drive light entrainment of the master circadian pacemaker of the suprachiasmatic nucleus, recent studies have proposed that entrainment of the mouse retinal clock is exclusively mediated by a UV-sen...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6415865/ https://www.ncbi.nlm.nih.gov/pubmed/30822304 http://dx.doi.org/10.1371/journal.pbio.2006211 |
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author | Calligaro, Hugo Coutanson, Christine Najjar, Raymond P. Mazzaro, Nadia Cooper, Howard M. Haddjeri, Nasser Felder-Schmittbuhl, Marie-Paule Dkhissi-Benyahya, Ouria |
author_facet | Calligaro, Hugo Coutanson, Christine Najjar, Raymond P. Mazzaro, Nadia Cooper, Howard M. Haddjeri, Nasser Felder-Schmittbuhl, Marie-Paule Dkhissi-Benyahya, Ouria |
author_sort | Calligaro, Hugo |
collection | PubMed |
description | While rods, cones, and intrinsically photosensitive melanopsin-containing ganglion cells (ipRGCs) all drive light entrainment of the master circadian pacemaker of the suprachiasmatic nucleus, recent studies have proposed that entrainment of the mouse retinal clock is exclusively mediated by a UV-sensitive photopigment, neuropsin (OPN5). Here, we report that the retinal circadian clock can be phase shifted by short duration and relatively low-irradiance monochromatic light in the visible part of the spectrum, up to 520 nm. Phase shifts exhibit a classical photon dose-response curve. Comparing the response of mouse models that specifically lack middle-wavelength (MW) cones, melanopsin, and/or rods, we found that only the absence of rods prevented light-induced phase shifts of the retinal clock, whereas light-induced phase shifts of locomotor activity are normal. In a “rod-only” mouse model, phase shifting response of the retinal clock to light is conserved. At shorter UV wavelengths, our results also reveal additional recruitment of short-wavelength (SW) cones and/or OPN5. These findings suggest a primary role of rod photoreceptors in the light response of the retinal clock in mammals. |
format | Online Article Text |
id | pubmed-6415865 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-64158652019-04-01 Rods contribute to the light-induced phase shift of the retinal clock in mammals Calligaro, Hugo Coutanson, Christine Najjar, Raymond P. Mazzaro, Nadia Cooper, Howard M. Haddjeri, Nasser Felder-Schmittbuhl, Marie-Paule Dkhissi-Benyahya, Ouria PLoS Biol Research Article While rods, cones, and intrinsically photosensitive melanopsin-containing ganglion cells (ipRGCs) all drive light entrainment of the master circadian pacemaker of the suprachiasmatic nucleus, recent studies have proposed that entrainment of the mouse retinal clock is exclusively mediated by a UV-sensitive photopigment, neuropsin (OPN5). Here, we report that the retinal circadian clock can be phase shifted by short duration and relatively low-irradiance monochromatic light in the visible part of the spectrum, up to 520 nm. Phase shifts exhibit a classical photon dose-response curve. Comparing the response of mouse models that specifically lack middle-wavelength (MW) cones, melanopsin, and/or rods, we found that only the absence of rods prevented light-induced phase shifts of the retinal clock, whereas light-induced phase shifts of locomotor activity are normal. In a “rod-only” mouse model, phase shifting response of the retinal clock to light is conserved. At shorter UV wavelengths, our results also reveal additional recruitment of short-wavelength (SW) cones and/or OPN5. These findings suggest a primary role of rod photoreceptors in the light response of the retinal clock in mammals. Public Library of Science 2019-03-01 /pmc/articles/PMC6415865/ /pubmed/30822304 http://dx.doi.org/10.1371/journal.pbio.2006211 Text en © 2019 Calligaro et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Calligaro, Hugo Coutanson, Christine Najjar, Raymond P. Mazzaro, Nadia Cooper, Howard M. Haddjeri, Nasser Felder-Schmittbuhl, Marie-Paule Dkhissi-Benyahya, Ouria Rods contribute to the light-induced phase shift of the retinal clock in mammals |
title | Rods contribute to the light-induced phase shift of the retinal clock in mammals |
title_full | Rods contribute to the light-induced phase shift of the retinal clock in mammals |
title_fullStr | Rods contribute to the light-induced phase shift of the retinal clock in mammals |
title_full_unstemmed | Rods contribute to the light-induced phase shift of the retinal clock in mammals |
title_short | Rods contribute to the light-induced phase shift of the retinal clock in mammals |
title_sort | rods contribute to the light-induced phase shift of the retinal clock in mammals |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6415865/ https://www.ncbi.nlm.nih.gov/pubmed/30822304 http://dx.doi.org/10.1371/journal.pbio.2006211 |
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