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Cl(−) homeodynamics in gap junction-coupled astrocytic networks on activation of GABAergic synapses

The electrophysiological properties and functional role of GABAergic signal transmission from neurons to the gap junction-coupled astrocytic network are still unclear. GABA-induced astrocytic Cl(−) flux has been hypothesized to affect the driving force for GABAergic transmission by modulating [Cl(−)...

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Detalles Bibliográficos
Autores principales: Egawa, Kiyoshi, Yamada, Junko, Furukawa, Tomonori, Yanagawa, Yuchio, Fukuda, Atsuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Science Inc 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3764636/
https://www.ncbi.nlm.nih.gov/pubmed/23732644
http://dx.doi.org/10.1113/jphysiol.2013.257162
Descripción
Sumario:The electrophysiological properties and functional role of GABAergic signal transmission from neurons to the gap junction-coupled astrocytic network are still unclear. GABA-induced astrocytic Cl(−) flux has been hypothesized to affect the driving force for GABAergic transmission by modulating [Cl(−)](o). Thus, revealing the properties of GABA-mediated astrocytic responses will deepen our understanding of GABAergic signal transmission. Here, we analysed the Cl(−) dynamics of neurons and astrocytes in CA1 hippocampal GABAergic tripartite synapses, using Cl(−) imaging during GABA application, and whole cell recordings from interneuron–astrocyte pairs in the stratum lacunosum-moleculare. Astrocytic [Cl(−)](i) was adjusted to physiological conditions (40 mm). Although GABA application evoked bidirectional Cl(−) flux via GABA(A) receptors and mouse GABA transporter 4 (mGAT4) in CA1 astrocytes, a train of interneuron firing induced only GABA(A) receptor-mediated inward currents in an adjacent astrocyte. A GAT1 inhibitor increased the interneuron firing-induced currents and induced bicuculline-insensitive, mGAT4 inhibitor-sensitive currents, suggesting that synaptic spillover of GABA predominantly induced the astrocytic Cl(−) efflux because GABA(A) receptors are localized near the synaptic clefts. This GABA-induced Cl(−) efflux was accompanied by Cl(−) siphoning via the gap junctions of the astrocytic network because gap junction inhibitors significantly reduced the interneuron firing-induced currents. Thus, Cl(−) efflux from astrocytes is homeostatically maintained within astrocytic networks. A gap junction inhibitor enhanced the activity-dependent depolarizing shifts of reversal potential of neuronal IPSCs evoked by repetitive stimulation to GABAergic synapses. These results suggest that Cl(−) conductance within the astrocytic network may contribute to maintaining GABAergic synaptic transmission by regulating [Cl(−)](o).