Cargando…
Light sets the brain’s daily clock by regional quickening and slowing of the molecular clockworks at dawn and dusk
How daily clocks in the brain are set by light to local environmental time and encode the seasons is not fully understood. The suprachiasmatic nucleus (SCN) is a central circadian clock in mammals that orchestrates physiology and behavior in tune with daily and seasonal light cycles. Here, we have f...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8687663/ https://www.ncbi.nlm.nih.gov/pubmed/34927581 http://dx.doi.org/10.7554/eLife.70137 |
_version_ | 1784618218863722496 |
---|---|
author | Kim, Suil McMahon, Douglas G |
author_facet | Kim, Suil McMahon, Douglas G |
author_sort | Kim, Suil |
collection | PubMed |
description | How daily clocks in the brain are set by light to local environmental time and encode the seasons is not fully understood. The suprachiasmatic nucleus (SCN) is a central circadian clock in mammals that orchestrates physiology and behavior in tune with daily and seasonal light cycles. Here, we have found that optogenetically simulated light input to explanted mouse SCN changes the waveform of the molecular clockworks from sinusoids in free-running conditions to highly asymmetrical shapes with accelerated synthetic (rising) phases and extended degradative (falling) phases marking clock advances and delays at simulated dawn and dusk. Daily waveform changes arise under ex vivo entrainment to simulated winter and summer photoperiods, and to non-24 hr periods. Ex vivo SCN imaging further suggests that acute waveform shifts are greatest in the ventrolateral SCN, while period effects are greatest in the dorsomedial SCN. Thus, circadian entrainment is encoded by SCN clock gene waveform changes that arise from spatiotemporally distinct intrinsic responses within the SCN neural network. |
format | Online Article Text |
id | pubmed-8687663 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-86876632021-12-22 Light sets the brain’s daily clock by regional quickening and slowing of the molecular clockworks at dawn and dusk Kim, Suil McMahon, Douglas G eLife Neuroscience How daily clocks in the brain are set by light to local environmental time and encode the seasons is not fully understood. The suprachiasmatic nucleus (SCN) is a central circadian clock in mammals that orchestrates physiology and behavior in tune with daily and seasonal light cycles. Here, we have found that optogenetically simulated light input to explanted mouse SCN changes the waveform of the molecular clockworks from sinusoids in free-running conditions to highly asymmetrical shapes with accelerated synthetic (rising) phases and extended degradative (falling) phases marking clock advances and delays at simulated dawn and dusk. Daily waveform changes arise under ex vivo entrainment to simulated winter and summer photoperiods, and to non-24 hr periods. Ex vivo SCN imaging further suggests that acute waveform shifts are greatest in the ventrolateral SCN, while period effects are greatest in the dorsomedial SCN. Thus, circadian entrainment is encoded by SCN clock gene waveform changes that arise from spatiotemporally distinct intrinsic responses within the SCN neural network. eLife Sciences Publications, Ltd 2021-12-20 /pmc/articles/PMC8687663/ /pubmed/34927581 http://dx.doi.org/10.7554/eLife.70137 Text en © 2021, Kim and McMahon https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Kim, Suil McMahon, Douglas G Light sets the brain’s daily clock by regional quickening and slowing of the molecular clockworks at dawn and dusk |
title | Light sets the brain’s daily clock by regional quickening and slowing of the molecular clockworks at dawn and dusk |
title_full | Light sets the brain’s daily clock by regional quickening and slowing of the molecular clockworks at dawn and dusk |
title_fullStr | Light sets the brain’s daily clock by regional quickening and slowing of the molecular clockworks at dawn and dusk |
title_full_unstemmed | Light sets the brain’s daily clock by regional quickening and slowing of the molecular clockworks at dawn and dusk |
title_short | Light sets the brain’s daily clock by regional quickening and slowing of the molecular clockworks at dawn and dusk |
title_sort | light sets the brain’s daily clock by regional quickening and slowing of the molecular clockworks at dawn and dusk |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8687663/ https://www.ncbi.nlm.nih.gov/pubmed/34927581 http://dx.doi.org/10.7554/eLife.70137 |
work_keys_str_mv | AT kimsuil lightsetsthebrainsdailyclockbyregionalquickeningandslowingofthemolecularclockworksatdawnanddusk AT mcmahondouglasg lightsetsthebrainsdailyclockbyregionalquickeningandslowingofthemolecularclockworksatdawnanddusk |