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Control of Ca(2+) signals by astrocyte nanoscale morphology at tripartite synapses

Much of the Ca(2+) activity in astrocytes is spatially restricted to microdomains and occurs in fine processes that form a complex anatomical meshwork, the so‐called spongiform domain. A growing body of literature indicates that those astrocytic Ca(2+) signals can influence the activity of neuronal...

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Autores principales: Denizot, Audrey, Arizono, Misa, Nägerl, U. Valentin, Berry, Hugues, De Schutter, Erik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9825906/
https://www.ncbi.nlm.nih.gov/pubmed/36097958
http://dx.doi.org/10.1002/glia.24258
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author Denizot, Audrey
Arizono, Misa
Nägerl, U. Valentin
Berry, Hugues
De Schutter, Erik
author_facet Denizot, Audrey
Arizono, Misa
Nägerl, U. Valentin
Berry, Hugues
De Schutter, Erik
author_sort Denizot, Audrey
collection PubMed
description Much of the Ca(2+) activity in astrocytes is spatially restricted to microdomains and occurs in fine processes that form a complex anatomical meshwork, the so‐called spongiform domain. A growing body of literature indicates that those astrocytic Ca(2+) signals can influence the activity of neuronal synapses and thus tune the flow of information through neuronal circuits. Because of technical difficulties in accessing the small spatial scale involved, the role of astrocyte morphology on Ca(2+) microdomain activity remains poorly understood. Here, we use computational tools and idealized 3D geometries of fine processes based on recent super‐resolution microscopy data to investigate the mechanistic link between astrocytic nanoscale morphology and local Ca(2+) activity. Simulations demonstrate that the nano‐morphology of astrocytic processes powerfully shapes the spatio‐temporal properties of Ca(2+) signals and promotes local Ca(2+) activity. The model predicts that this effect is attenuated upon astrocytic swelling, hallmark of brain diseases, which we confirm experimentally in hypo‐osmotic conditions. Upon repeated neurotransmitter release events, the model predicts that swelling hinders astrocytic signal propagation. Overall, this study highlights the influence of the complex morphology of astrocytes at the nanoscale and its remodeling in pathological conditions on neuron‐astrocyte communication at so‐called tripartite synapses, where astrocytic processes come into close contact with pre‐ and postsynaptic structures.
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spelling pubmed-98259062023-01-09 Control of Ca(2+) signals by astrocyte nanoscale morphology at tripartite synapses Denizot, Audrey Arizono, Misa Nägerl, U. Valentin Berry, Hugues De Schutter, Erik Glia Research Articles Much of the Ca(2+) activity in astrocytes is spatially restricted to microdomains and occurs in fine processes that form a complex anatomical meshwork, the so‐called spongiform domain. A growing body of literature indicates that those astrocytic Ca(2+) signals can influence the activity of neuronal synapses and thus tune the flow of information through neuronal circuits. Because of technical difficulties in accessing the small spatial scale involved, the role of astrocyte morphology on Ca(2+) microdomain activity remains poorly understood. Here, we use computational tools and idealized 3D geometries of fine processes based on recent super‐resolution microscopy data to investigate the mechanistic link between astrocytic nanoscale morphology and local Ca(2+) activity. Simulations demonstrate that the nano‐morphology of astrocytic processes powerfully shapes the spatio‐temporal properties of Ca(2+) signals and promotes local Ca(2+) activity. The model predicts that this effect is attenuated upon astrocytic swelling, hallmark of brain diseases, which we confirm experimentally in hypo‐osmotic conditions. Upon repeated neurotransmitter release events, the model predicts that swelling hinders astrocytic signal propagation. Overall, this study highlights the influence of the complex morphology of astrocytes at the nanoscale and its remodeling in pathological conditions on neuron‐astrocyte communication at so‐called tripartite synapses, where astrocytic processes come into close contact with pre‐ and postsynaptic structures. John Wiley & Sons, Inc. 2022-09-13 2022-12 /pmc/articles/PMC9825906/ /pubmed/36097958 http://dx.doi.org/10.1002/glia.24258 Text en © 2022 The Authors. GLIA published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Research Articles
Denizot, Audrey
Arizono, Misa
Nägerl, U. Valentin
Berry, Hugues
De Schutter, Erik
Control of Ca(2+) signals by astrocyte nanoscale morphology at tripartite synapses
title Control of Ca(2+) signals by astrocyte nanoscale morphology at tripartite synapses
title_full Control of Ca(2+) signals by astrocyte nanoscale morphology at tripartite synapses
title_fullStr Control of Ca(2+) signals by astrocyte nanoscale morphology at tripartite synapses
title_full_unstemmed Control of Ca(2+) signals by astrocyte nanoscale morphology at tripartite synapses
title_short Control of Ca(2+) signals by astrocyte nanoscale morphology at tripartite synapses
title_sort control of ca(2+) signals by astrocyte nanoscale morphology at tripartite synapses
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9825906/
https://www.ncbi.nlm.nih.gov/pubmed/36097958
http://dx.doi.org/10.1002/glia.24258
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