Cargando…
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...
Autores principales: | , , , , , , , |
---|---|
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 |
_version_ | 1783545980544614400 |
---|---|
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. |
format | Online Article Text |
id | pubmed-7291822 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT fernandezdiegocarlos retinalinnervationtunescircuitsthatdrivenonphoticentrainmenttofood AT komalruchi retinalinnervationtunescircuitsthatdrivenonphoticentrainmenttofood AT langeljennifer retinalinnervationtunescircuitsthatdrivenonphoticentrainmenttofood AT majun retinalinnervationtunescircuitsthatdrivenonphoticentrainmenttofood AT duyphanq retinalinnervationtunescircuitsthatdrivenonphoticentrainmenttofood AT penzomarioa retinalinnervationtunescircuitsthatdrivenonphoticentrainmenttofood AT zhaohaiqing retinalinnervationtunescircuitsthatdrivenonphoticentrainmenttofood AT hattarsamer retinalinnervationtunescircuitsthatdrivenonphoticentrainmenttofood |