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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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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
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author Egawa, Kiyoshi
Yamada, Junko
Furukawa, Tomonori
Yanagawa, Yuchio
Fukuda, Atsuo
author_facet Egawa, Kiyoshi
Yamada, Junko
Furukawa, Tomonori
Yanagawa, Yuchio
Fukuda, Atsuo
author_sort Egawa, Kiyoshi
collection PubMed
description 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).
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spelling pubmed-37646362013-12-02 Cl(−) homeodynamics in gap junction-coupled astrocytic networks on activation of GABAergic synapses Egawa, Kiyoshi Yamada, Junko Furukawa, Tomonori Yanagawa, Yuchio Fukuda, Atsuo J Physiol Neuroscience: Cellular/Molecular 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). Blackwell Science Inc 2013-08-15 2013-06-03 /pmc/articles/PMC3764636/ /pubmed/23732644 http://dx.doi.org/10.1113/jphysiol.2013.257162 Text en © 2013 The Authors. The Journal of Physiology published by John Wiley & Sons Ltd on behalf of The Physiological Society. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. https://creativecommons.org/licenses/by/4.0/ © 2013 The Authors. The Journal of Physiology published by John Wiley & Sons Ltd on behalf of The Physiological Society. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Neuroscience: Cellular/Molecular
Egawa, Kiyoshi
Yamada, Junko
Furukawa, Tomonori
Yanagawa, Yuchio
Fukuda, Atsuo
Cl(−) homeodynamics in gap junction-coupled astrocytic networks on activation of GABAergic synapses
title Cl(−) homeodynamics in gap junction-coupled astrocytic networks on activation of GABAergic synapses
title_full Cl(−) homeodynamics in gap junction-coupled astrocytic networks on activation of GABAergic synapses
title_fullStr Cl(−) homeodynamics in gap junction-coupled astrocytic networks on activation of GABAergic synapses
title_full_unstemmed Cl(−) homeodynamics in gap junction-coupled astrocytic networks on activation of GABAergic synapses
title_short Cl(−) homeodynamics in gap junction-coupled astrocytic networks on activation of GABAergic synapses
title_sort cl(−) homeodynamics in gap junction-coupled astrocytic networks on activation of gabaergic synapses
topic Neuroscience: Cellular/Molecular
url 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
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