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Neuronal network activity controls microglial process surveillance in awake mice via norepinephrine signaling

Microglia dynamically survey the brain parenchyma. Microglial processes interact with neuronal elements; however, the role neuronal network activity plays in regulating microglial dynamics is not entirely clear. Most studies of microglial dynamics use either slice preparations or in vivo imaging in...

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Autores principales: Liu, Yong U., Ying, Yanlu, Li, Yujiao, Eyo, Ukpong B., Chen, Tingjun, Zheng, Jiaying, Umpierre, Anthony D., Zhu, Jia, Bosco, Dale B., Dong, Hailong, Wu, Long-Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6858573/
https://www.ncbi.nlm.nih.gov/pubmed/31636449
http://dx.doi.org/10.1038/s41593-019-0511-3
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author Liu, Yong U.
Ying, Yanlu
Li, Yujiao
Eyo, Ukpong B.
Chen, Tingjun
Zheng, Jiaying
Umpierre, Anthony D.
Zhu, Jia
Bosco, Dale B.
Dong, Hailong
Wu, Long-Jun
author_facet Liu, Yong U.
Ying, Yanlu
Li, Yujiao
Eyo, Ukpong B.
Chen, Tingjun
Zheng, Jiaying
Umpierre, Anthony D.
Zhu, Jia
Bosco, Dale B.
Dong, Hailong
Wu, Long-Jun
author_sort Liu, Yong U.
collection PubMed
description Microglia dynamically survey the brain parenchyma. Microglial processes interact with neuronal elements; however, the role neuronal network activity plays in regulating microglial dynamics is not entirely clear. Most studies of microglial dynamics use either slice preparations or in vivo imaging in anesthetized mice. Here we demonstrate that microglia in awake mice have relatively reduced process area and surveillance territory, and that reduced neuronal activity under general anesthesia increases microglial process velocity, extension and territory surveillance. Similarly, reductions in local neuronal activity through sensory deprivation or optogenetic inhibition increase microglial process surveillance. Using pharmacological and chemogenetic approaches, we demonstrate that reduced norepinephrine signaling is necessary for these increases in microglial process surveillance. These findings indicate that under basal physiological conditions noradrenergic tone in awake mice suppresses microglial process surveillance. Our results emphasize the importance of awake imaging for studying microglia–neuron interactions and demonstrate how neuronal activity influences microglial process dynamics.
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spelling pubmed-68585732020-04-21 Neuronal network activity controls microglial process surveillance in awake mice via norepinephrine signaling Liu, Yong U. Ying, Yanlu Li, Yujiao Eyo, Ukpong B. Chen, Tingjun Zheng, Jiaying Umpierre, Anthony D. Zhu, Jia Bosco, Dale B. Dong, Hailong Wu, Long-Jun Nat Neurosci Article Microglia dynamically survey the brain parenchyma. Microglial processes interact with neuronal elements; however, the role neuronal network activity plays in regulating microglial dynamics is not entirely clear. Most studies of microglial dynamics use either slice preparations or in vivo imaging in anesthetized mice. Here we demonstrate that microglia in awake mice have relatively reduced process area and surveillance territory, and that reduced neuronal activity under general anesthesia increases microglial process velocity, extension and territory surveillance. Similarly, reductions in local neuronal activity through sensory deprivation or optogenetic inhibition increase microglial process surveillance. Using pharmacological and chemogenetic approaches, we demonstrate that reduced norepinephrine signaling is necessary for these increases in microglial process surveillance. These findings indicate that under basal physiological conditions noradrenergic tone in awake mice suppresses microglial process surveillance. Our results emphasize the importance of awake imaging for studying microglia–neuron interactions and demonstrate how neuronal activity influences microglial process dynamics. 2019-10-21 2019-11 /pmc/articles/PMC6858573/ /pubmed/31636449 http://dx.doi.org/10.1038/s41593-019-0511-3 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Liu, Yong U.
Ying, Yanlu
Li, Yujiao
Eyo, Ukpong B.
Chen, Tingjun
Zheng, Jiaying
Umpierre, Anthony D.
Zhu, Jia
Bosco, Dale B.
Dong, Hailong
Wu, Long-Jun
Neuronal network activity controls microglial process surveillance in awake mice via norepinephrine signaling
title Neuronal network activity controls microglial process surveillance in awake mice via norepinephrine signaling
title_full Neuronal network activity controls microglial process surveillance in awake mice via norepinephrine signaling
title_fullStr Neuronal network activity controls microglial process surveillance in awake mice via norepinephrine signaling
title_full_unstemmed Neuronal network activity controls microglial process surveillance in awake mice via norepinephrine signaling
title_short Neuronal network activity controls microglial process surveillance in awake mice via norepinephrine signaling
title_sort neuronal network activity controls microglial process surveillance in awake mice via norepinephrine signaling
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6858573/
https://www.ncbi.nlm.nih.gov/pubmed/31636449
http://dx.doi.org/10.1038/s41593-019-0511-3
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