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Retinal innervation tunes circuits that drive nonphotic entrainment to food

Daily changes in light and food availability are major time-cues influencing circadian timing(1). Little is known, however, about the circuits integrating these time-cues to drive a coherent circadian output(1–3). Here, we investigated whether retinal inputs modulate the entrainment to non-photic cu...

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Autores principales: Fernandez, Diego Carlos, Komal, Ruchi, Langel, Jennifer, Ma, Jun, Duy, Phan Q., Penzo, Mario A., Zhao, Haiqing, Hattar, Samer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7291822/
https://www.ncbi.nlm.nih.gov/pubmed/32404998
http://dx.doi.org/10.1038/s41586-020-2204-1
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author Fernandez, Diego Carlos
Komal, Ruchi
Langel, Jennifer
Ma, Jun
Duy, Phan Q.
Penzo, Mario A.
Zhao, Haiqing
Hattar, Samer
author_facet Fernandez, Diego Carlos
Komal, Ruchi
Langel, Jennifer
Ma, Jun
Duy, Phan Q.
Penzo, Mario A.
Zhao, Haiqing
Hattar, Samer
author_sort Fernandez, Diego Carlos
collection PubMed
description Daily changes in light and food availability are major time-cues influencing circadian timing(1). Little is known, however, about the circuits integrating these time-cues to drive a coherent circadian output(1–3). Here, we investigated whether retinal inputs modulate the entrainment to non-photic cues, such as time-restricted feeding. Photic information is relayed to the suprachiasmatic nucleus (SCN), which houses the central circadian pacemaker, and the intergeniculate leaflet (IGL) through intrinsically-photosensitive retinal ganglion cells (ipRGCs)(4). Adult mice lacking ipRGCs since early-postnatal stages displayed impaired entrainment to time-restricted feeding, whereas ablating ipRGCs at later stages had no effect. Early-postnatal ipRGC innervation influences neuropeptide Y (NPY)-expressing IGL neurons, guiding the functional IGL(NPY)-SCN circuit assembly. Moreover, silencing the IGL(NPY) neurons in adult animals mimicked the deficits induced by early-postnatal ipRGC ablation, and acute inhibition of IGL(NPY) terminals in the SCN decreased food-anticipatory activity. Thus, early-postnatal ipRGC innervation tunes the IGL(NPY)-SCN circuit to allow entrainment to time-restricted feeding.
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spelling pubmed-72918222020-10-22 Retinal innervation tunes circuits that drive nonphotic entrainment to food Fernandez, Diego Carlos Komal, Ruchi Langel, Jennifer Ma, Jun Duy, Phan Q. Penzo, Mario A. Zhao, Haiqing Hattar, Samer Nature Article Daily changes in light and food availability are major time-cues influencing circadian timing(1). Little is known, however, about the circuits integrating these time-cues to drive a coherent circadian output(1–3). Here, we investigated whether retinal inputs modulate the entrainment to non-photic cues, such as time-restricted feeding. Photic information is relayed to the suprachiasmatic nucleus (SCN), which houses the central circadian pacemaker, and the intergeniculate leaflet (IGL) through intrinsically-photosensitive retinal ganglion cells (ipRGCs)(4). Adult mice lacking ipRGCs since early-postnatal stages displayed impaired entrainment to time-restricted feeding, whereas ablating ipRGCs at later stages had no effect. Early-postnatal ipRGC innervation influences neuropeptide Y (NPY)-expressing IGL neurons, guiding the functional IGL(NPY)-SCN circuit assembly. Moreover, silencing the IGL(NPY) neurons in adult animals mimicked the deficits induced by early-postnatal ipRGC ablation, and acute inhibition of IGL(NPY) terminals in the SCN decreased food-anticipatory activity. Thus, early-postnatal ipRGC innervation tunes the IGL(NPY)-SCN circuit to allow entrainment to time-restricted feeding. 2020-04-22 2020-05 /pmc/articles/PMC7291822/ /pubmed/32404998 http://dx.doi.org/10.1038/s41586-020-2204-1 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Fernandez, Diego Carlos
Komal, Ruchi
Langel, Jennifer
Ma, Jun
Duy, Phan Q.
Penzo, Mario A.
Zhao, Haiqing
Hattar, Samer
Retinal innervation tunes circuits that drive nonphotic entrainment to food
title Retinal innervation tunes circuits that drive nonphotic entrainment to food
title_full Retinal innervation tunes circuits that drive nonphotic entrainment to food
title_fullStr Retinal innervation tunes circuits that drive nonphotic entrainment to food
title_full_unstemmed Retinal innervation tunes circuits that drive nonphotic entrainment to food
title_short Retinal innervation tunes circuits that drive nonphotic entrainment to food
title_sort retinal innervation tunes circuits that drive nonphotic entrainment to food
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7291822/
https://www.ncbi.nlm.nih.gov/pubmed/32404998
http://dx.doi.org/10.1038/s41586-020-2204-1
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