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Microglial calcium signaling is attuned to neuronal activity in awake mice

Microglial calcium signaling underlies a number of key physiological and pathological processes in situ, but has not been studied in vivo in awake mice. Using multiple GCaMP6 variants targeted to microglia, we assessed how microglial calcium signaling responds to alterations in neuronal activity acr...

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Autores principales: Umpierre, Anthony D, Bystrom, Lauren L, Ying, Yanlu, Liu, Yong U, Worrell, Gregory, Wu, Long-Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7402678/
https://www.ncbi.nlm.nih.gov/pubmed/32716294
http://dx.doi.org/10.7554/eLife.56502
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author Umpierre, Anthony D
Bystrom, Lauren L
Ying, Yanlu
Liu, Yong U
Worrell, Gregory
Wu, Long-Jun
author_facet Umpierre, Anthony D
Bystrom, Lauren L
Ying, Yanlu
Liu, Yong U
Worrell, Gregory
Wu, Long-Jun
author_sort Umpierre, Anthony D
collection PubMed
description Microglial calcium signaling underlies a number of key physiological and pathological processes in situ, but has not been studied in vivo in awake mice. Using multiple GCaMP6 variants targeted to microglia, we assessed how microglial calcium signaling responds to alterations in neuronal activity across a wide range. We find that only a small subset of microglial somata and processes exhibited spontaneous calcium transients in a chronic window preparation. However, hyperactive shifts in neuronal activity (kainate status epilepticus and CaMKIIa Gq DREADD activation) triggered increased microglial process calcium signaling, often concomitant with process extension. Additionally, hypoactive shifts in neuronal activity (isoflurane anesthesia and CaMKIIa Gi DREADD activation) also increased microglial process calcium signaling. Under hypoactive neuronal conditions, microglia also exhibited process extension and outgrowth with greater calcium signaling. Our work reveals that microglia have highly distinct microdomain signaling, and that processes specifically respond to bi-directional shifts in neuronal activity through increased calcium signaling.
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spelling pubmed-74026782020-08-06 Microglial calcium signaling is attuned to neuronal activity in awake mice Umpierre, Anthony D Bystrom, Lauren L Ying, Yanlu Liu, Yong U Worrell, Gregory Wu, Long-Jun eLife Neuroscience Microglial calcium signaling underlies a number of key physiological and pathological processes in situ, but has not been studied in vivo in awake mice. Using multiple GCaMP6 variants targeted to microglia, we assessed how microglial calcium signaling responds to alterations in neuronal activity across a wide range. We find that only a small subset of microglial somata and processes exhibited spontaneous calcium transients in a chronic window preparation. However, hyperactive shifts in neuronal activity (kainate status epilepticus and CaMKIIa Gq DREADD activation) triggered increased microglial process calcium signaling, often concomitant with process extension. Additionally, hypoactive shifts in neuronal activity (isoflurane anesthesia and CaMKIIa Gi DREADD activation) also increased microglial process calcium signaling. Under hypoactive neuronal conditions, microglia also exhibited process extension and outgrowth with greater calcium signaling. Our work reveals that microglia have highly distinct microdomain signaling, and that processes specifically respond to bi-directional shifts in neuronal activity through increased calcium signaling. eLife Sciences Publications, Ltd 2020-07-27 /pmc/articles/PMC7402678/ /pubmed/32716294 http://dx.doi.org/10.7554/eLife.56502 Text en © 2020, Umpierre 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
Umpierre, Anthony D
Bystrom, Lauren L
Ying, Yanlu
Liu, Yong U
Worrell, Gregory
Wu, Long-Jun
Microglial calcium signaling is attuned to neuronal activity in awake mice
title Microglial calcium signaling is attuned to neuronal activity in awake mice
title_full Microglial calcium signaling is attuned to neuronal activity in awake mice
title_fullStr Microglial calcium signaling is attuned to neuronal activity in awake mice
title_full_unstemmed Microglial calcium signaling is attuned to neuronal activity in awake mice
title_short Microglial calcium signaling is attuned to neuronal activity in awake mice
title_sort microglial calcium signaling is attuned to neuronal activity in awake mice
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7402678/
https://www.ncbi.nlm.nih.gov/pubmed/32716294
http://dx.doi.org/10.7554/eLife.56502
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