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Glial Ca2+signaling links endocytosis to K+ buffering around neuronal somas to regulate excitability

Author(s)
Weiss Sharabi, Shirley; Melom, Jan Elizabeth; Ormerod, Kiel G; Zhang, Yao; Littleton, J. Troy
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Creative Commons Attribution 4.0 International license https://creativecommons.org/licenses/by/4.0/
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Abstract
Glial-neuronal signaling at synapses is widely studied, but how glia interact with neuronal somas to regulate their activity is unclear. Drosophila cortex glia are restricted to brain regions devoid of synapses, providing an opportunity to characterize interactions with neuronal somas. Mutations in the cortex glial NCKXzydecoelevate basal Ca2+, predisposing animals to seizure-like behavior. To determine how cortex glial Ca2+signaling controls neuronal excitability, we performed an in vivo modifier screen of the NCKXzydecoseizure phenotype. We show that elevation of glial Ca2+causes hyperactivation of calcineurin-dependent endocytosis and accumulation of early endosomes. Knockdown of sandman, a K2P channel, recapitulates NCKXzydecoseizures. Indeed, sandman expression on cortex glial membranes is substantially reduced in NCKXzydecomutants, indicating enhanced internalization of sandman predisposes animals to seizures. These data provide an unexpected link between glial Ca2+signaling and the well-known role of glia in K+buffering as a key mechanism for regulating neuronal excitability.
Date issued
2019-04
URI
https://hdl.handle.net/1721.1/125501
Department
Picower Institute for Learning and Memory; Massachusetts Institute of Technology. Department of Biology; Massachusetts Institute of Technology. Department of Brain and Cognitive Sciences
Journal
eLife
Publisher
eLife Sciences Publications, Ltd
Citation
Weiss, Shirley et al. “Glial Ca2+signaling links endocytosis to K+ buffering around neuronal somas to regulate excitability.” eLife 8 (2019): e44186 © 2019 The Author(s)
Version: Final published version
ISSN
1534-4983

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