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Spontaneous Ca(2+) Fluctuations Arise in Thin Astrocytic Processes With Real 3D Geometry

Fluctuations of cytosolic Ca(2+) concentration in astrocytes are regarded as a critical non-neuronal signal to regulate neuronal functions. Although such fluctuations can be evoked by neuronal activity, rhythmic astrocytic Ca(2+) oscillations may also spontaneously arise. Experimental studies hint t...

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Autores principales: Héja, László, Szabó, Zsolt, Péter, Márton, Kardos, Julianna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7957061/
https://www.ncbi.nlm.nih.gov/pubmed/33732110
http://dx.doi.org/10.3389/fncel.2021.617989
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author Héja, László
Szabó, Zsolt
Péter, Márton
Kardos, Julianna
author_facet Héja, László
Szabó, Zsolt
Péter, Márton
Kardos, Julianna
author_sort Héja, László
collection PubMed
description Fluctuations of cytosolic Ca(2+) concentration in astrocytes are regarded as a critical non-neuronal signal to regulate neuronal functions. Although such fluctuations can be evoked by neuronal activity, rhythmic astrocytic Ca(2+) oscillations may also spontaneously arise. Experimental studies hint that these spontaneous astrocytic Ca(2+) oscillations may lie behind different kinds of emerging neuronal synchronized activities, like epileptogenic bursts or slow-wave rhythms. Despite the potential importance of spontaneous Ca(2+) oscillations in astrocytes, the mechanism by which they develop is poorly understood. Using simple 3D synapse models and kinetic data of astrocytic Glu transporters (EAATs) and the Na(+)/Ca(2+) exchanger (NCX), we have previously shown that NCX activity alone can generate markedly stable, spontaneous Ca(2+) oscillation in the astrocytic leaflet microdomain. Here, we extend that model by incorporating experimentally determined real 3D geometries of 208 excitatory synapses reconstructed from publicly available ultra-resolution electron microscopy datasets. Our simulations predict that the surface/volume ratio (SVR) of peri-synaptic astrocytic processes prominently dictates whether NCX-mediated spontaneous Ca(2+) oscillations emerge. We also show that increased levels of intracellular astrocytic Na(+) concentration facilitate the appearance of Ca(2+) fluctuations. These results further support the principal role of the dynamical reshaping of astrocyte processes in the generation of intrinsic Ca(2+) oscillations and their spreading over larger astrocytic compartments.
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spelling pubmed-79570612021-03-16 Spontaneous Ca(2+) Fluctuations Arise in Thin Astrocytic Processes With Real 3D Geometry Héja, László Szabó, Zsolt Péter, Márton Kardos, Julianna Front Cell Neurosci Cellular Neuroscience Fluctuations of cytosolic Ca(2+) concentration in astrocytes are regarded as a critical non-neuronal signal to regulate neuronal functions. Although such fluctuations can be evoked by neuronal activity, rhythmic astrocytic Ca(2+) oscillations may also spontaneously arise. Experimental studies hint that these spontaneous astrocytic Ca(2+) oscillations may lie behind different kinds of emerging neuronal synchronized activities, like epileptogenic bursts or slow-wave rhythms. Despite the potential importance of spontaneous Ca(2+) oscillations in astrocytes, the mechanism by which they develop is poorly understood. Using simple 3D synapse models and kinetic data of astrocytic Glu transporters (EAATs) and the Na(+)/Ca(2+) exchanger (NCX), we have previously shown that NCX activity alone can generate markedly stable, spontaneous Ca(2+) oscillation in the astrocytic leaflet microdomain. Here, we extend that model by incorporating experimentally determined real 3D geometries of 208 excitatory synapses reconstructed from publicly available ultra-resolution electron microscopy datasets. Our simulations predict that the surface/volume ratio (SVR) of peri-synaptic astrocytic processes prominently dictates whether NCX-mediated spontaneous Ca(2+) oscillations emerge. We also show that increased levels of intracellular astrocytic Na(+) concentration facilitate the appearance of Ca(2+) fluctuations. These results further support the principal role of the dynamical reshaping of astrocyte processes in the generation of intrinsic Ca(2+) oscillations and their spreading over larger astrocytic compartments. Frontiers Media S.A. 2021-03-01 /pmc/articles/PMC7957061/ /pubmed/33732110 http://dx.doi.org/10.3389/fncel.2021.617989 Text en Copyright © 2021 Héja, Szabó, Péter and Kardos. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cellular Neuroscience
Héja, László
Szabó, Zsolt
Péter, Márton
Kardos, Julianna
Spontaneous Ca(2+) Fluctuations Arise in Thin Astrocytic Processes With Real 3D Geometry
title Spontaneous Ca(2+) Fluctuations Arise in Thin Astrocytic Processes With Real 3D Geometry
title_full Spontaneous Ca(2+) Fluctuations Arise in Thin Astrocytic Processes With Real 3D Geometry
title_fullStr Spontaneous Ca(2+) Fluctuations Arise in Thin Astrocytic Processes With Real 3D Geometry
title_full_unstemmed Spontaneous Ca(2+) Fluctuations Arise in Thin Astrocytic Processes With Real 3D Geometry
title_short Spontaneous Ca(2+) Fluctuations Arise in Thin Astrocytic Processes With Real 3D Geometry
title_sort spontaneous ca(2+) fluctuations arise in thin astrocytic processes with real 3d geometry
topic Cellular Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7957061/
https://www.ncbi.nlm.nih.gov/pubmed/33732110
http://dx.doi.org/10.3389/fncel.2021.617989
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