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New tools for investigating astrocyte-to-neuron communication

Gray matter protoplasmic astrocytes extend very thin processes and establish close contacts with synapses. It has been suggested that the release of neuroactive gliotransmitters at the tripartite synapse contributes to information processing. However, the concept of calcium (Ca(2+))-dependent gliotr...

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Autores principales: Li, Dongdong, Agulhon, Cendra, Schmidt, Elke, Oheim, Martin, Ropert, Nicole
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3810613/
https://www.ncbi.nlm.nih.gov/pubmed/24194698
http://dx.doi.org/10.3389/fncel.2013.00193
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author Li, Dongdong
Agulhon, Cendra
Schmidt, Elke
Oheim, Martin
Ropert, Nicole
author_facet Li, Dongdong
Agulhon, Cendra
Schmidt, Elke
Oheim, Martin
Ropert, Nicole
author_sort Li, Dongdong
collection PubMed
description Gray matter protoplasmic astrocytes extend very thin processes and establish close contacts with synapses. It has been suggested that the release of neuroactive gliotransmitters at the tripartite synapse contributes to information processing. However, the concept of calcium (Ca(2+))-dependent gliotransmitter release from astrocytes, and the release mechanisms are being debated. Studying astrocytes in their natural environment is challenging because: (i) astrocytes are electrically silent; (ii) astrocytes and neurons express an overlapping repertoire of transmembrane receptors; (iii) the size of astrocyte processes in contact with synapses are below the resolution of confocal and two-photon microscopes (iv) bulk-loading techniques using fluorescent Ca(2+) indicators lack cellular specificity. In this review, we will discuss some limitations of conventional methodologies and highlight the interest of novel tools and approaches for studying gliotransmission. Genetically encoded Ca(2+) indicators (GECIs), light-gated channels, and exogenous receptors are being developed to selectively read out and stimulate astrocyte activity. Our review discusses emerging perspectives on: (i) the complexity of astrocyte Ca(2+) signaling revealed by GECIs; (ii) new pharmacogenetic and optogenetic approaches to activate specific Ca(2+) signaling pathways in astrocytes; (iii) classical and new techniques to monitor vesicle fusion in cultured astrocytes; (iv) possible strategies to express specifically reporter genes in astrocytes.
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spelling pubmed-38106132013-11-05 New tools for investigating astrocyte-to-neuron communication Li, Dongdong Agulhon, Cendra Schmidt, Elke Oheim, Martin Ropert, Nicole Front Cell Neurosci Neuroscience Gray matter protoplasmic astrocytes extend very thin processes and establish close contacts with synapses. It has been suggested that the release of neuroactive gliotransmitters at the tripartite synapse contributes to information processing. However, the concept of calcium (Ca(2+))-dependent gliotransmitter release from astrocytes, and the release mechanisms are being debated. Studying astrocytes in their natural environment is challenging because: (i) astrocytes are electrically silent; (ii) astrocytes and neurons express an overlapping repertoire of transmembrane receptors; (iii) the size of astrocyte processes in contact with synapses are below the resolution of confocal and two-photon microscopes (iv) bulk-loading techniques using fluorescent Ca(2+) indicators lack cellular specificity. In this review, we will discuss some limitations of conventional methodologies and highlight the interest of novel tools and approaches for studying gliotransmission. Genetically encoded Ca(2+) indicators (GECIs), light-gated channels, and exogenous receptors are being developed to selectively read out and stimulate astrocyte activity. Our review discusses emerging perspectives on: (i) the complexity of astrocyte Ca(2+) signaling revealed by GECIs; (ii) new pharmacogenetic and optogenetic approaches to activate specific Ca(2+) signaling pathways in astrocytes; (iii) classical and new techniques to monitor vesicle fusion in cultured astrocytes; (iv) possible strategies to express specifically reporter genes in astrocytes. Frontiers Media S.A. 2013-10-29 /pmc/articles/PMC3810613/ /pubmed/24194698 http://dx.doi.org/10.3389/fncel.2013.00193 Text en Copyright © 2013 Li, Agulhon, Schmidt, Oheim and Ropert. http://creativecommons.org/licenses/by/3.0/ 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) or licensor 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 Neuroscience
Li, Dongdong
Agulhon, Cendra
Schmidt, Elke
Oheim, Martin
Ropert, Nicole
New tools for investigating astrocyte-to-neuron communication
title New tools for investigating astrocyte-to-neuron communication
title_full New tools for investigating astrocyte-to-neuron communication
title_fullStr New tools for investigating astrocyte-to-neuron communication
title_full_unstemmed New tools for investigating astrocyte-to-neuron communication
title_short New tools for investigating astrocyte-to-neuron communication
title_sort new tools for investigating astrocyte-to-neuron communication
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3810613/
https://www.ncbi.nlm.nih.gov/pubmed/24194698
http://dx.doi.org/10.3389/fncel.2013.00193
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