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Subtle modulation of ongoing calcium dynamics in astrocytic microdomains by sensory inputs

Astrocytes communicate with neurons through their processes. In vitro experiments have demonstrated that astrocytic processes exhibit calcium activity both spontaneously and in response to external stimuli; however, it has not been fully determined whether and how astrocytic subcellular domains resp...

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Autores principales: Asada, Akiko, Ujita, Sakiko, Nakayama, Ryota, Oba, Shigeyuki, Ishii, Shin, Matsuki, Norio, Ikegaya, Yuji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4632942/
https://www.ncbi.nlm.nih.gov/pubmed/26438730
http://dx.doi.org/10.14814/phy2.12454
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author Asada, Akiko
Ujita, Sakiko
Nakayama, Ryota
Oba, Shigeyuki
Ishii, Shin
Matsuki, Norio
Ikegaya, Yuji
author_facet Asada, Akiko
Ujita, Sakiko
Nakayama, Ryota
Oba, Shigeyuki
Ishii, Shin
Matsuki, Norio
Ikegaya, Yuji
author_sort Asada, Akiko
collection PubMed
description Astrocytes communicate with neurons through their processes. In vitro experiments have demonstrated that astrocytic processes exhibit calcium activity both spontaneously and in response to external stimuli; however, it has not been fully determined whether and how astrocytic subcellular domains respond to sensory input in vivo. We visualized the calcium signals in astrocytes in the primary visual cortex of awake, head-fixed mice. Bias-free analyses of two-photon imaging data revealed that calcium activity prevailed in astrocytic subcellular domains, was coordinated with variable spot-like patterns, and was dominantly spontaneous. Indeed, visual stimuli did not affect the frequency of calcium domain activity, but it increased the domain size, whereas tetrodotoxin reduced the sizes of spontaneous calcium domains and abolished their visual responses. The “evoked” domain activity exhibited no apparent orientation tuning and was distributed unevenly within the cell, constituting multiple active hotspots that were often also recruited in spontaneous activity. The hotspots existed dominantly in the somata and endfeet of astrocytes. Thus, the patterns of astrocytic calcium dynamics are intrinsically constrained and are subject to minor but significant modulation by sensory input.
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spelling pubmed-46329422015-11-09 Subtle modulation of ongoing calcium dynamics in astrocytic microdomains by sensory inputs Asada, Akiko Ujita, Sakiko Nakayama, Ryota Oba, Shigeyuki Ishii, Shin Matsuki, Norio Ikegaya, Yuji Physiol Rep Original Research Astrocytes communicate with neurons through their processes. In vitro experiments have demonstrated that astrocytic processes exhibit calcium activity both spontaneously and in response to external stimuli; however, it has not been fully determined whether and how astrocytic subcellular domains respond to sensory input in vivo. We visualized the calcium signals in astrocytes in the primary visual cortex of awake, head-fixed mice. Bias-free analyses of two-photon imaging data revealed that calcium activity prevailed in astrocytic subcellular domains, was coordinated with variable spot-like patterns, and was dominantly spontaneous. Indeed, visual stimuli did not affect the frequency of calcium domain activity, but it increased the domain size, whereas tetrodotoxin reduced the sizes of spontaneous calcium domains and abolished their visual responses. The “evoked” domain activity exhibited no apparent orientation tuning and was distributed unevenly within the cell, constituting multiple active hotspots that were often also recruited in spontaneous activity. The hotspots existed dominantly in the somata and endfeet of astrocytes. Thus, the patterns of astrocytic calcium dynamics are intrinsically constrained and are subject to minor but significant modulation by sensory input. John Wiley & Sons, Ltd 2015-10-05 /pmc/articles/PMC4632942/ /pubmed/26438730 http://dx.doi.org/10.14814/phy2.12454 Text en © 2015 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of the American Physiological Society and The Physiological Society. http://creativecommons.org/licenses/by/4.0/ 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 Original Research
Asada, Akiko
Ujita, Sakiko
Nakayama, Ryota
Oba, Shigeyuki
Ishii, Shin
Matsuki, Norio
Ikegaya, Yuji
Subtle modulation of ongoing calcium dynamics in astrocytic microdomains by sensory inputs
title Subtle modulation of ongoing calcium dynamics in astrocytic microdomains by sensory inputs
title_full Subtle modulation of ongoing calcium dynamics in astrocytic microdomains by sensory inputs
title_fullStr Subtle modulation of ongoing calcium dynamics in astrocytic microdomains by sensory inputs
title_full_unstemmed Subtle modulation of ongoing calcium dynamics in astrocytic microdomains by sensory inputs
title_short Subtle modulation of ongoing calcium dynamics in astrocytic microdomains by sensory inputs
title_sort subtle modulation of ongoing calcium dynamics in astrocytic microdomains by sensory inputs
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4632942/
https://www.ncbi.nlm.nih.gov/pubmed/26438730
http://dx.doi.org/10.14814/phy2.12454
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