Distinct ipRGC subpopulations mediate light’s acute and circadian effects on body temperature and sleep
The light environment greatly impacts human alertness, mood, and cognition by both acute regulation of physiology and indirect alignment of circadian rhythms. These processes require the melanopsin-expressing intrinsically photosensitive retinal ganglion cells (ipRGCs), but the relevant downstream b...
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doaj-352a158e440f4e6aa38a0f92fbff5bf82021-05-05T17:47:20ZengeLife Sciences Publications LtdeLife2050-084X2019-07-01810.7554/eLife.44358Distinct ipRGC subpopulations mediate light’s acute and circadian effects on body temperature and sleepAlan C Rupp0https://orcid.org/0000-0001-5363-4494Michelle Ren1Cara M Altimus2Diego C Fernandez3Melissa Richardson4Fred Turek5Samer Hattar6https://orcid.org/0000-0002-3124-9525Tiffany M Schmidt7https://orcid.org/0000-0002-4791-6775Department of Biology, Johns Hopkins University, Baltimore, United StatesDepartment of Neurobiology, Northwestern University, Evanston, United StatesDepartment of Biology, Johns Hopkins University, Baltimore, United StatesDepartment of Biology, Johns Hopkins University, Baltimore, United StatesDepartment of Biology, Johns Hopkins University, Baltimore, United StatesDepartment of Neurobiology, Northwestern University, Evanston, United StatesDepartment of Biology, Johns Hopkins University, Baltimore, United States; Department of Neuroscience, Johns Hopkins University, Baltimore, United StatesDepartment of Neurobiology, Northwestern University, Evanston, United StatesThe light environment greatly impacts human alertness, mood, and cognition by both acute regulation of physiology and indirect alignment of circadian rhythms. These processes require the melanopsin-expressing intrinsically photosensitive retinal ganglion cells (ipRGCs), but the relevant downstream brain areas involved remain elusive. ipRGCs project widely in the brain, including to the central circadian pacemaker, the suprachiasmatic nucleus (SCN). Here we show that body temperature and sleep responses to acute light exposure are absent after genetic ablation of all ipRGCs except a subpopulation that projects to the SCN. Furthermore, by chemogenetic activation of the ipRGCs that avoid the SCN, we show that these cells are sufficient for acute changes in body temperature. Our results challenge the idea that the SCN is a major relay for the acute effects of light on non-image forming behaviors and identify the sensory cells that initiate light’s profound effects on body temperature and sleep.https://elifesciences.org/articles/44358circadianSuprachiasmatic NucleussleeptemperaturemelanopsinipRGC |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Alan C Rupp Michelle Ren Cara M Altimus Diego C Fernandez Melissa Richardson Fred Turek Samer Hattar Tiffany M Schmidt |
spellingShingle |
Alan C Rupp Michelle Ren Cara M Altimus Diego C Fernandez Melissa Richardson Fred Turek Samer Hattar Tiffany M Schmidt Distinct ipRGC subpopulations mediate light’s acute and circadian effects on body temperature and sleep eLife circadian Suprachiasmatic Nucleus sleep temperature melanopsin ipRGC |
author_facet |
Alan C Rupp Michelle Ren Cara M Altimus Diego C Fernandez Melissa Richardson Fred Turek Samer Hattar Tiffany M Schmidt |
author_sort |
Alan C Rupp |
title |
Distinct ipRGC subpopulations mediate light’s acute and circadian effects on body temperature and sleep |
title_short |
Distinct ipRGC subpopulations mediate light’s acute and circadian effects on body temperature and sleep |
title_full |
Distinct ipRGC subpopulations mediate light’s acute and circadian effects on body temperature and sleep |
title_fullStr |
Distinct ipRGC subpopulations mediate light’s acute and circadian effects on body temperature and sleep |
title_full_unstemmed |
Distinct ipRGC subpopulations mediate light’s acute and circadian effects on body temperature and sleep |
title_sort |
distinct iprgc subpopulations mediate light’s acute and circadian effects on body temperature and sleep |
publisher |
eLife Sciences Publications Ltd |
series |
eLife |
issn |
2050-084X |
publishDate |
2019-07-01 |
description |
The light environment greatly impacts human alertness, mood, and cognition by both acute regulation of physiology and indirect alignment of circadian rhythms. These processes require the melanopsin-expressing intrinsically photosensitive retinal ganglion cells (ipRGCs), but the relevant downstream brain areas involved remain elusive. ipRGCs project widely in the brain, including to the central circadian pacemaker, the suprachiasmatic nucleus (SCN). Here we show that body temperature and sleep responses to acute light exposure are absent after genetic ablation of all ipRGCs except a subpopulation that projects to the SCN. Furthermore, by chemogenetic activation of the ipRGCs that avoid the SCN, we show that these cells are sufficient for acute changes in body temperature. Our results challenge the idea that the SCN is a major relay for the acute effects of light on non-image forming behaviors and identify the sensory cells that initiate light’s profound effects on body temperature and sleep. |
topic |
circadian Suprachiasmatic Nucleus sleep temperature melanopsin ipRGC |
url |
https://elifesciences.org/articles/44358 |
work_keys_str_mv |
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