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Astrocytes modulate thalamic sensory processing via mGlu2 receptor activation

Astrocytes possess many of the same signalling molecules as neurons. However, the role of astrocytes in information processing, if any, is unknown. Using electrophysiological and imaging methods, we report the first evidence that astrocytes modulate neuronal sensory inhibition in the rodent thalamus...

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Detalles Bibliográficos
Autores principales: Copeland, C.S., Wall, T.M., Sims, R.E., Neale, S.A., Nisenbaum, E., Parri, H.R., Salt, T.E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Pergamon Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5480778/
https://www.ncbi.nlm.nih.gov/pubmed/28416443
http://dx.doi.org/10.1016/j.neuropharm.2017.04.019
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author Copeland, C.S.
Wall, T.M.
Sims, R.E.
Neale, S.A.
Nisenbaum, E.
Parri, H.R.
Salt, T.E.
author_facet Copeland, C.S.
Wall, T.M.
Sims, R.E.
Neale, S.A.
Nisenbaum, E.
Parri, H.R.
Salt, T.E.
author_sort Copeland, C.S.
collection PubMed
description Astrocytes possess many of the same signalling molecules as neurons. However, the role of astrocytes in information processing, if any, is unknown. Using electrophysiological and imaging methods, we report the first evidence that astrocytes modulate neuronal sensory inhibition in the rodent thalamus. We found that mGlu2 receptor activity reduces inhibitory transmission from the thalamic reticular nucleus to the somatosensory ventrobasal thalamus (VB): mIPSC frequencies in VB slices were reduced by the Group II mGlu receptor agonist LY354740, an effect potentiated by mGlu2 positive allosteric modulator (PAM) LY487379 co-application (30 nM LY354740: 10.0 ± 1.6% reduction; 30 nM LY354740 & 30 μM LY487379: 34.6 ± 5.2% reduction). We then showed activation of mGlu2 receptors on astrocytes: astrocytic intracellular calcium levels were elevated by the Group II agonist, which were further potentiated upon mGlu2 PAM co-application (300 nM LY354740: ratio amplitude 0.016 ± 0.002; 300 nM LY354740 & 30 μM LY487379: ratio amplitude 0.035 ± 0.003). We then demonstrated mGlu2-dependent astrocytic disinhibition of VB neurons in vivo: VB neuronal responses to vibrissae stimulation trains were disinhibited by the Group II agonist and the mGlu2 PAM (LY354740: 156 ± 12% of control; LY487379: 144 ± 10% of control). Presence of the glial inhibitor fluorocitrate abolished the mGlu2 PAM effect (91 ± 5% of control), suggesting the mGlu2 component to the Group II effect can be attributed to activation of mGlu2 receptors localised on astrocytic processes within the VB. Gating of thalamocortical function via astrocyte activation represents a novel sensory processing mechanism. As this thalamocortical circuitry is important in discriminative processes, this demonstrates the importance of astrocytes in synaptic processes underlying attention and cognition.
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spelling pubmed-54807782017-07-15 Astrocytes modulate thalamic sensory processing via mGlu2 receptor activation Copeland, C.S. Wall, T.M. Sims, R.E. Neale, S.A. Nisenbaum, E. Parri, H.R. Salt, T.E. Neuropharmacology Article Astrocytes possess many of the same signalling molecules as neurons. However, the role of astrocytes in information processing, if any, is unknown. Using electrophysiological and imaging methods, we report the first evidence that astrocytes modulate neuronal sensory inhibition in the rodent thalamus. We found that mGlu2 receptor activity reduces inhibitory transmission from the thalamic reticular nucleus to the somatosensory ventrobasal thalamus (VB): mIPSC frequencies in VB slices were reduced by the Group II mGlu receptor agonist LY354740, an effect potentiated by mGlu2 positive allosteric modulator (PAM) LY487379 co-application (30 nM LY354740: 10.0 ± 1.6% reduction; 30 nM LY354740 & 30 μM LY487379: 34.6 ± 5.2% reduction). We then showed activation of mGlu2 receptors on astrocytes: astrocytic intracellular calcium levels were elevated by the Group II agonist, which were further potentiated upon mGlu2 PAM co-application (300 nM LY354740: ratio amplitude 0.016 ± 0.002; 300 nM LY354740 & 30 μM LY487379: ratio amplitude 0.035 ± 0.003). We then demonstrated mGlu2-dependent astrocytic disinhibition of VB neurons in vivo: VB neuronal responses to vibrissae stimulation trains were disinhibited by the Group II agonist and the mGlu2 PAM (LY354740: 156 ± 12% of control; LY487379: 144 ± 10% of control). Presence of the glial inhibitor fluorocitrate abolished the mGlu2 PAM effect (91 ± 5% of control), suggesting the mGlu2 component to the Group II effect can be attributed to activation of mGlu2 receptors localised on astrocytic processes within the VB. Gating of thalamocortical function via astrocyte activation represents a novel sensory processing mechanism. As this thalamocortical circuitry is important in discriminative processes, this demonstrates the importance of astrocytes in synaptic processes underlying attention and cognition. Pergamon Press 2017-07-15 /pmc/articles/PMC5480778/ /pubmed/28416443 http://dx.doi.org/10.1016/j.neuropharm.2017.04.019 Text en © 2017 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Copeland, C.S.
Wall, T.M.
Sims, R.E.
Neale, S.A.
Nisenbaum, E.
Parri, H.R.
Salt, T.E.
Astrocytes modulate thalamic sensory processing via mGlu2 receptor activation
title Astrocytes modulate thalamic sensory processing via mGlu2 receptor activation
title_full Astrocytes modulate thalamic sensory processing via mGlu2 receptor activation
title_fullStr Astrocytes modulate thalamic sensory processing via mGlu2 receptor activation
title_full_unstemmed Astrocytes modulate thalamic sensory processing via mGlu2 receptor activation
title_short Astrocytes modulate thalamic sensory processing via mGlu2 receptor activation
title_sort astrocytes modulate thalamic sensory processing via mglu2 receptor activation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5480778/
https://www.ncbi.nlm.nih.gov/pubmed/28416443
http://dx.doi.org/10.1016/j.neuropharm.2017.04.019
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