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Ecdysone acts through cortex glia to regulate sleep in Drosophila
Steroid hormones are attractive candidates for transmitting long-range signals to affect behavior. These lipid-soluble molecules derived from dietary cholesterol easily penetrate the brain and act through nuclear hormone receptors (NHRs) that function as transcription factors. To determine the exten...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9928426/ https://www.ncbi.nlm.nih.gov/pubmed/36719183 http://dx.doi.org/10.7554/eLife.81723 |
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author | Li, Yongjun Haynes, Paula Zhang, Shirley L Yue, Zhifeng Sehgal, Amita |
author_facet | Li, Yongjun Haynes, Paula Zhang, Shirley L Yue, Zhifeng Sehgal, Amita |
author_sort | Li, Yongjun |
collection | PubMed |
description | Steroid hormones are attractive candidates for transmitting long-range signals to affect behavior. These lipid-soluble molecules derived from dietary cholesterol easily penetrate the brain and act through nuclear hormone receptors (NHRs) that function as transcription factors. To determine the extent to which NHRs affect sleep:wake cycles, we knocked down each of the 18 highly conserved NHRs found in Drosophila adults and report that the ecdysone receptor (EcR) and its direct downstream NHR Eip75B (E75) act in glia to regulate the rhythm and amount of sleep. Given that ecdysone synthesis genes have little to no expression in the fly brain, ecdysone appears to act as a long-distance signal and our data suggest that it enters the brain more at night. Anti-EcR staining localizes to the cortex glia in the brain and functional screening of glial subtypes revealed that EcR functions in adult cortex glia to affect sleep. Cortex glia are implicated in lipid metabolism, which appears to be relevant for actions of ecdysone as ecdysone treatment mobilizes lipid droplets (LDs), and knockdown of glial EcR results in more LDs. In addition, sleep-promoting effects of exogenous ecdysone are diminished in lsd-2 mutant flies, which are lean and deficient in lipid accumulation. We propose that ecdysone is a systemic secreted factor that modulates sleep by stimulating lipid metabolism in cortex glia. |
format | Online Article Text |
id | pubmed-9928426 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-99284262023-02-15 Ecdysone acts through cortex glia to regulate sleep in Drosophila Li, Yongjun Haynes, Paula Zhang, Shirley L Yue, Zhifeng Sehgal, Amita eLife Neuroscience Steroid hormones are attractive candidates for transmitting long-range signals to affect behavior. These lipid-soluble molecules derived from dietary cholesterol easily penetrate the brain and act through nuclear hormone receptors (NHRs) that function as transcription factors. To determine the extent to which NHRs affect sleep:wake cycles, we knocked down each of the 18 highly conserved NHRs found in Drosophila adults and report that the ecdysone receptor (EcR) and its direct downstream NHR Eip75B (E75) act in glia to regulate the rhythm and amount of sleep. Given that ecdysone synthesis genes have little to no expression in the fly brain, ecdysone appears to act as a long-distance signal and our data suggest that it enters the brain more at night. Anti-EcR staining localizes to the cortex glia in the brain and functional screening of glial subtypes revealed that EcR functions in adult cortex glia to affect sleep. Cortex glia are implicated in lipid metabolism, which appears to be relevant for actions of ecdysone as ecdysone treatment mobilizes lipid droplets (LDs), and knockdown of glial EcR results in more LDs. In addition, sleep-promoting effects of exogenous ecdysone are diminished in lsd-2 mutant flies, which are lean and deficient in lipid accumulation. We propose that ecdysone is a systemic secreted factor that modulates sleep by stimulating lipid metabolism in cortex glia. eLife Sciences Publications, Ltd 2023-01-31 /pmc/articles/PMC9928426/ /pubmed/36719183 http://dx.doi.org/10.7554/eLife.81723 Text en © 2023, Li et al 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 Li, Yongjun Haynes, Paula Zhang, Shirley L Yue, Zhifeng Sehgal, Amita Ecdysone acts through cortex glia to regulate sleep in Drosophila |
title | Ecdysone acts through cortex glia to regulate sleep in Drosophila |
title_full | Ecdysone acts through cortex glia to regulate sleep in Drosophila |
title_fullStr | Ecdysone acts through cortex glia to regulate sleep in Drosophila |
title_full_unstemmed | Ecdysone acts through cortex glia to regulate sleep in Drosophila |
title_short | Ecdysone acts through cortex glia to regulate sleep in Drosophila |
title_sort | ecdysone acts through cortex glia to regulate sleep in drosophila |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9928426/ https://www.ncbi.nlm.nih.gov/pubmed/36719183 http://dx.doi.org/10.7554/eLife.81723 |
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