Mutation of a NCKX Eliminates Glial Microdomain Calcium Oscillations and Enhances Seizure Susceptibility
Glia exhibit spontaneous and activity-dependent fluctuations in intracellular Ca[superscript 2+], yet it is unclear whether glial Ca[superscript 2+] oscillations are required during neuronal signaling. Somatic glial Ca[superscript 2+] waves are primarily mediated by the release of intracellular Ca[s...
| Main Authors: | , |
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| Other Authors: | |
| Format: | Article |
| Language: | en_US |
| Published: |
Society for Neuroscience
2013
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| Online Access: | http://hdl.handle.net/1721.1/80313 https://orcid.org/0000-0001-5576-2887 |
| Summary: | Glia exhibit spontaneous and activity-dependent fluctuations in intracellular Ca[superscript 2+], yet it is unclear whether glial Ca[superscript 2+] oscillations are required during neuronal signaling. Somatic glial Ca[superscript 2+] waves are primarily mediated by the release of intracellular Ca[superscript 2+] stores, and their relative importance in normal brain physiology has been disputed. Recently, near-membrane microdomain Ca[superscript 2+] transients were identified in fine astrocytic processes and found to arise via an intracellular store-independent process. Here, we describe the identification of rapid, near-membrane Ca[superscript 2+] oscillations in Drosophila cortex glia of the CNS. In a screen for temperature-sensitive conditional seizure mutants, we identified a glial-specific Na[superscript +]/Ca[superscript 2+], K[superscript +] exchanger (zydeco) that is required for microdomain Ca[superscript 2+] oscillatory activity. We found that zydeco mutant animals exhibit increased susceptibility to seizures in response to a variety of environmental stimuli, and that zydeco is required acutely in cortex glia to regulate seizure susceptibility. We also found that glial expression of calmodulin is required for stress-induced seizures in zydeco mutants, suggesting a Ca[superscript 2+]/calmodulin-dependent glial signaling pathway underlies glial–neuronal communication. These studies demonstrate that microdomain glial Ca[superscript 2+] oscillations require NCKX-mediated plasma membrane Ca[superscript 2+] flux, and that acute dysregulation of glial Ca[superscript 2+] signaling triggers seizures. |
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