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TRPA1 channels regulate astrocyte resting calcium levels and inhibitory synapse efficacy via GAT-3

Astrocytes contribute to the formation and function of synapses and are found throughout the brain where they display intracellular store mediated Ca(2+) signals. Here, using a membrane tethered genetically encoded calcium indicator (Lck-GCaMP3), we report the serendipitous discovery of a novel Ca(2...

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Detalles Bibliográficos
Autores principales: Shigetomi, Eiji, Tong, Xiaoping, Kwan, Kelvin Y., Corey, David P., Khakh, Baljit S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3282183/
https://www.ncbi.nlm.nih.gov/pubmed/22158513
http://dx.doi.org/10.1038/nn.3000
Descripción
Sumario:Astrocytes contribute to the formation and function of synapses and are found throughout the brain where they display intracellular store mediated Ca(2+) signals. Here, using a membrane tethered genetically encoded calcium indicator (Lck-GCaMP3), we report the serendipitous discovery of a novel Ca(2+) signal in rat hippocampal astrocyte-neuron co-cultures. We found that TRPA1 channel mediated Ca(2+) fluxes give rise to frequent and highly localised near membrane “spotty” Ca(2+) microdomains that contribute significantly to resting Ca(2+) levels of astrocytes. Mechanistic evaluations in brain slices show that decreasing astrocyte resting Ca(2+) levels mediated by TRPA1 channels decreased interneuron inhibitory synapse efficacy by reducing GABA transport via GAT-3, thus elevating extracellular GABA levels. Our data indicate how a novel transmembrane Ca(2+) source (TRPA1) targets a transporter (GAT-3) in astrocytes to regulate inhibitory synapses.