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Endocytosis at the Drosophila blood–brain barrier as a function for sleep

Glia are important modulators of neural activity, yet few studies link glia to sleep regulation. We find that blocking activity of the endocytosis protein, dynamin, in adult Drosophila glia increases sleep and enhances sleep need, manifest as resistance to sleep deprivation. Surface glia comprising...

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Autores principales: Artiushin, Gregory, Zhang, Shirley L, Tricoire, Hervé, Sehgal, Amita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6255390/
https://www.ncbi.nlm.nih.gov/pubmed/30475209
http://dx.doi.org/10.7554/eLife.43326
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author Artiushin, Gregory
Zhang, Shirley L
Tricoire, Hervé
Sehgal, Amita
author_facet Artiushin, Gregory
Zhang, Shirley L
Tricoire, Hervé
Sehgal, Amita
author_sort Artiushin, Gregory
collection PubMed
description Glia are important modulators of neural activity, yet few studies link glia to sleep regulation. We find that blocking activity of the endocytosis protein, dynamin, in adult Drosophila glia increases sleep and enhances sleep need, manifest as resistance to sleep deprivation. Surface glia comprising the fly equivalent of the blood-brain barrier (BBB) mediate the effect of dynamin on sleep. Blocking dynamin in the surface glia causes ultrastructural changes, albeit without compromising the integrity of the barrier. Supporting a role for endocytic trafficking in sleep, a screen of Rab GTPases identifies sleep-modulating effects of the recycling endosome Rab11 in surface glia. We also find that endocytosis is increased in BBB glia during sleep and reflects sleep need. We propose that endocytic trafficking through the BBB represents a function of sleep.
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spelling pubmed-62553902018-11-27 Endocytosis at the Drosophila blood–brain barrier as a function for sleep Artiushin, Gregory Zhang, Shirley L Tricoire, Hervé Sehgal, Amita eLife Neuroscience Glia are important modulators of neural activity, yet few studies link glia to sleep regulation. We find that blocking activity of the endocytosis protein, dynamin, in adult Drosophila glia increases sleep and enhances sleep need, manifest as resistance to sleep deprivation. Surface glia comprising the fly equivalent of the blood-brain barrier (BBB) mediate the effect of dynamin on sleep. Blocking dynamin in the surface glia causes ultrastructural changes, albeit without compromising the integrity of the barrier. Supporting a role for endocytic trafficking in sleep, a screen of Rab GTPases identifies sleep-modulating effects of the recycling endosome Rab11 in surface glia. We also find that endocytosis is increased in BBB glia during sleep and reflects sleep need. We propose that endocytic trafficking through the BBB represents a function of sleep. eLife Sciences Publications, Ltd 2018-11-26 /pmc/articles/PMC6255390/ /pubmed/30475209 http://dx.doi.org/10.7554/eLife.43326 Text en © 2018, Artiushin 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
Artiushin, Gregory
Zhang, Shirley L
Tricoire, Hervé
Sehgal, Amita
Endocytosis at the Drosophila blood–brain barrier as a function for sleep
title Endocytosis at the Drosophila blood–brain barrier as a function for sleep
title_full Endocytosis at the Drosophila blood–brain barrier as a function for sleep
title_fullStr Endocytosis at the Drosophila blood–brain barrier as a function for sleep
title_full_unstemmed Endocytosis at the Drosophila blood–brain barrier as a function for sleep
title_short Endocytosis at the Drosophila blood–brain barrier as a function for sleep
title_sort endocytosis at the drosophila blood–brain barrier as a function for sleep
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6255390/
https://www.ncbi.nlm.nih.gov/pubmed/30475209
http://dx.doi.org/10.7554/eLife.43326
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