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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2020
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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. |
format | Online Article Text |
id | pubmed-7402678 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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