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Sensory and cortical activation of distinct glial cell subtypes in the somatosensory thalamus of young rats

The rodent ventrobasal (VB) thalamus receives sensory inputs from the whiskers and projects to the cortex, from which it receives reciprocal excitatory afferents. Much is known about the properties and functional roles of these glutamatergic inputs to thalamocortical neurons in the VB, but no data a...

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Autores principales: Parri, H Rheinallt, Gould, Timothy M, Crunelli, Vincenzo
Formato: Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2909395/
https://www.ncbi.nlm.nih.gov/pubmed/20608967
http://dx.doi.org/10.1111/j.1460-9568.2010.07281.x
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author Parri, H Rheinallt
Gould, Timothy M
Crunelli, Vincenzo
author_facet Parri, H Rheinallt
Gould, Timothy M
Crunelli, Vincenzo
author_sort Parri, H Rheinallt
collection PubMed
description The rodent ventrobasal (VB) thalamus receives sensory inputs from the whiskers and projects to the cortex, from which it receives reciprocal excitatory afferents. Much is known about the properties and functional roles of these glutamatergic inputs to thalamocortical neurons in the VB, but no data are available on how these afferents can affect thalamic glial cells. In this study, we used combined electrophysiological recordings and intracellular calcium ([Ca(2+)](i)) imaging to investigate glial cell responses to synaptic afferent stimulation. VB thalamus glial cells can be divided into two groups based on their [Ca(2+)](i) and electrophysiological responses to sensory and corticothalamic stimulation. One group consists of astrocytes, which stain positively for S100B and preferentially load with SR101, have linear current–voltage relations and low input resistance, show no voltage-dependent [Ca(2+)](i) responses, but express mGluR5-dependent [Ca(2+)](i) transients following stimulation of the sensory and/or corticothalamic excitatory afferent pathways. Cells of the other glial group, by contrast, stain positively for NG2, and are characterized by high input resistance, the presence of voltage-dependent [Ca(2+)](i) elevations and voltage-gated inward currents. There were no synaptically induced [Ca(2+)](i) elevations in these cells under control conditions. These results show that thalamic glial cell responses to synaptic input exhibit different properties to those of thalamocortical neurons. As VB astrocytes can respond to synaptic stimulation and signal to neighbouring neurons, this glial cell organization may have functional implications for the processing of somatosensory information and modulation of behavioural state-dependent thalamocortical network activities.
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spelling pubmed-29093952010-07-29 Sensory and cortical activation of distinct glial cell subtypes in the somatosensory thalamus of young rats Parri, H Rheinallt Gould, Timothy M Crunelli, Vincenzo Eur J Neurosci Synaptic Mechanisms The rodent ventrobasal (VB) thalamus receives sensory inputs from the whiskers and projects to the cortex, from which it receives reciprocal excitatory afferents. Much is known about the properties and functional roles of these glutamatergic inputs to thalamocortical neurons in the VB, but no data are available on how these afferents can affect thalamic glial cells. In this study, we used combined electrophysiological recordings and intracellular calcium ([Ca(2+)](i)) imaging to investigate glial cell responses to synaptic afferent stimulation. VB thalamus glial cells can be divided into two groups based on their [Ca(2+)](i) and electrophysiological responses to sensory and corticothalamic stimulation. One group consists of astrocytes, which stain positively for S100B and preferentially load with SR101, have linear current–voltage relations and low input resistance, show no voltage-dependent [Ca(2+)](i) responses, but express mGluR5-dependent [Ca(2+)](i) transients following stimulation of the sensory and/or corticothalamic excitatory afferent pathways. Cells of the other glial group, by contrast, stain positively for NG2, and are characterized by high input resistance, the presence of voltage-dependent [Ca(2+)](i) elevations and voltage-gated inward currents. There were no synaptically induced [Ca(2+)](i) elevations in these cells under control conditions. These results show that thalamic glial cell responses to synaptic input exhibit different properties to those of thalamocortical neurons. As VB astrocytes can respond to synaptic stimulation and signal to neighbouring neurons, this glial cell organization may have functional implications for the processing of somatosensory information and modulation of behavioural state-dependent thalamocortical network activities. Blackwell Publishing Ltd 2010-07 /pmc/articles/PMC2909395/ /pubmed/20608967 http://dx.doi.org/10.1111/j.1460-9568.2010.07281.x Text en Journal compilation © 2010 Federation of European Neuroscience Societies and Blackwell Publishing Ltd http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.
spellingShingle Synaptic Mechanisms
Parri, H Rheinallt
Gould, Timothy M
Crunelli, Vincenzo
Sensory and cortical activation of distinct glial cell subtypes in the somatosensory thalamus of young rats
title Sensory and cortical activation of distinct glial cell subtypes in the somatosensory thalamus of young rats
title_full Sensory and cortical activation of distinct glial cell subtypes in the somatosensory thalamus of young rats
title_fullStr Sensory and cortical activation of distinct glial cell subtypes in the somatosensory thalamus of young rats
title_full_unstemmed Sensory and cortical activation of distinct glial cell subtypes in the somatosensory thalamus of young rats
title_short Sensory and cortical activation of distinct glial cell subtypes in the somatosensory thalamus of young rats
title_sort sensory and cortical activation of distinct glial cell subtypes in the somatosensory thalamus of young rats
topic Synaptic Mechanisms
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2909395/
https://www.ncbi.nlm.nih.gov/pubmed/20608967
http://dx.doi.org/10.1111/j.1460-9568.2010.07281.x
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