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AANAT1 functions in astrocytes to regulate sleep homeostasis

How the brain controls the need and acquisition of recovery sleep after prolonged wakefulness is an important issue in sleep research. The monoamines serotonin and dopamine are key regulators of sleep in mammals and in Drosophila. We found that the enzyme arylalkylamine N-acetyltransferase 1 (AANAT1...

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Autores principales: Davla, Sejal, Artiushin, Gregory, Li, Yongjun, Chitsaz, Daryan, Li, Sally, Sehgal, Amita, van Meyel, Donald J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7550187/
https://www.ncbi.nlm.nih.gov/pubmed/32955431
http://dx.doi.org/10.7554/eLife.53994
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author Davla, Sejal
Artiushin, Gregory
Li, Yongjun
Chitsaz, Daryan
Li, Sally
Sehgal, Amita
van Meyel, Donald J
author_facet Davla, Sejal
Artiushin, Gregory
Li, Yongjun
Chitsaz, Daryan
Li, Sally
Sehgal, Amita
van Meyel, Donald J
author_sort Davla, Sejal
collection PubMed
description How the brain controls the need and acquisition of recovery sleep after prolonged wakefulness is an important issue in sleep research. The monoamines serotonin and dopamine are key regulators of sleep in mammals and in Drosophila. We found that the enzyme arylalkylamine N-acetyltransferase 1 (AANAT1) is expressed by Drosophila astrocytes and specific subsets of neurons in the adult brain. AANAT1 acetylates monoamines and inactivates them, and we found that AANAT1 limited the accumulation of serotonin and dopamine in the brain upon sleep deprivation (SD). Loss of AANAT1 from astrocytes, but not from neurons, caused flies to increase their daytime recovery sleep following overnight SD. Together, these findings demonstrate a crucial role for AANAT1 and astrocytes in the regulation of monoamine bioavailability and homeostatic sleep.
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spelling pubmed-75501872020-10-14 AANAT1 functions in astrocytes to regulate sleep homeostasis Davla, Sejal Artiushin, Gregory Li, Yongjun Chitsaz, Daryan Li, Sally Sehgal, Amita van Meyel, Donald J eLife Neuroscience How the brain controls the need and acquisition of recovery sleep after prolonged wakefulness is an important issue in sleep research. The monoamines serotonin and dopamine are key regulators of sleep in mammals and in Drosophila. We found that the enzyme arylalkylamine N-acetyltransferase 1 (AANAT1) is expressed by Drosophila astrocytes and specific subsets of neurons in the adult brain. AANAT1 acetylates monoamines and inactivates them, and we found that AANAT1 limited the accumulation of serotonin and dopamine in the brain upon sleep deprivation (SD). Loss of AANAT1 from astrocytes, but not from neurons, caused flies to increase their daytime recovery sleep following overnight SD. Together, these findings demonstrate a crucial role for AANAT1 and astrocytes in the regulation of monoamine bioavailability and homeostatic sleep. eLife Sciences Publications, Ltd 2020-09-21 /pmc/articles/PMC7550187/ /pubmed/32955431 http://dx.doi.org/10.7554/eLife.53994 Text en © 2020, Davla et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Davla, Sejal
Artiushin, Gregory
Li, Yongjun
Chitsaz, Daryan
Li, Sally
Sehgal, Amita
van Meyel, Donald J
AANAT1 functions in astrocytes to regulate sleep homeostasis
title AANAT1 functions in astrocytes to regulate sleep homeostasis
title_full AANAT1 functions in astrocytes to regulate sleep homeostasis
title_fullStr AANAT1 functions in astrocytes to regulate sleep homeostasis
title_full_unstemmed AANAT1 functions in astrocytes to regulate sleep homeostasis
title_short AANAT1 functions in astrocytes to regulate sleep homeostasis
title_sort aanat1 functions in astrocytes to regulate sleep homeostasis
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7550187/
https://www.ncbi.nlm.nih.gov/pubmed/32955431
http://dx.doi.org/10.7554/eLife.53994
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