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Extracellular ATP release predominantly mediates Ca(2+) communication locally in highly organised, stellate-Like patterned networks of adult human astrocytes

The ‘Astrocyte Network’ and the understanding of its communication has been posed as a new grand challenge to be investigated by contemporary science. However, communication studies in astrocyte networks have investigated traditional petri-dish in vitro culture models where cells are closely packed...

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Detalles Bibliográficos
Autores principales: Li, Si, Graham, E. Scott, Unsworth, Charles P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10547170/
https://www.ncbi.nlm.nih.gov/pubmed/37788259
http://dx.doi.org/10.1371/journal.pone.0289350
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author Li, Si
Graham, E. Scott
Unsworth, Charles P.
author_facet Li, Si
Graham, E. Scott
Unsworth, Charles P.
author_sort Li, Si
collection PubMed
description The ‘Astrocyte Network’ and the understanding of its communication has been posed as a new grand challenge to be investigated by contemporary science. However, communication studies in astrocyte networks have investigated traditional petri-dish in vitro culture models where cells are closely packed and can deviate from the stellate form observed in the brain. Using novel cell patterning approaches, highly organised, regular grid networks of astrocytes on chip, to single-cell fidelity are constructed, permitting a stellate-like in vitro network model to be realised. By stimulating the central cell with a single UV nanosecond laser pulse, the initiation/propagation pathways of stellate-like networks are re-explored. The authors investigate the mechanisms of intercellular Ca(2+) communication and discover that stellate-like networks of adult human astrocytes in vitro actually exploit extracellular ATP release as their dominant propagation pathway to cells in the network locally; being observed even down to the nearest neighbour and next nearest neighbouring cells—contrary to the reported gap junction. This discovery has significant ramifications to many neurological conditions such as epilepsy, stroke and aggressive astrocytomas where gap junctions can be targeted. In cases where such gap junction targeting has failed, this new finding suggests that these conditions should be re-visited and the ATP transmission pathway targeted instead.
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spelling pubmed-105471702023-10-04 Extracellular ATP release predominantly mediates Ca(2+) communication locally in highly organised, stellate-Like patterned networks of adult human astrocytes Li, Si Graham, E. Scott Unsworth, Charles P. PLoS One Research Article The ‘Astrocyte Network’ and the understanding of its communication has been posed as a new grand challenge to be investigated by contemporary science. However, communication studies in astrocyte networks have investigated traditional petri-dish in vitro culture models where cells are closely packed and can deviate from the stellate form observed in the brain. Using novel cell patterning approaches, highly organised, regular grid networks of astrocytes on chip, to single-cell fidelity are constructed, permitting a stellate-like in vitro network model to be realised. By stimulating the central cell with a single UV nanosecond laser pulse, the initiation/propagation pathways of stellate-like networks are re-explored. The authors investigate the mechanisms of intercellular Ca(2+) communication and discover that stellate-like networks of adult human astrocytes in vitro actually exploit extracellular ATP release as their dominant propagation pathway to cells in the network locally; being observed even down to the nearest neighbour and next nearest neighbouring cells—contrary to the reported gap junction. This discovery has significant ramifications to many neurological conditions such as epilepsy, stroke and aggressive astrocytomas where gap junctions can be targeted. In cases where such gap junction targeting has failed, this new finding suggests that these conditions should be re-visited and the ATP transmission pathway targeted instead. Public Library of Science 2023-10-03 /pmc/articles/PMC10547170/ /pubmed/37788259 http://dx.doi.org/10.1371/journal.pone.0289350 Text en © 2023 Li et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Li, Si
Graham, E. Scott
Unsworth, Charles P.
Extracellular ATP release predominantly mediates Ca(2+) communication locally in highly organised, stellate-Like patterned networks of adult human astrocytes
title Extracellular ATP release predominantly mediates Ca(2+) communication locally in highly organised, stellate-Like patterned networks of adult human astrocytes
title_full Extracellular ATP release predominantly mediates Ca(2+) communication locally in highly organised, stellate-Like patterned networks of adult human astrocytes
title_fullStr Extracellular ATP release predominantly mediates Ca(2+) communication locally in highly organised, stellate-Like patterned networks of adult human astrocytes
title_full_unstemmed Extracellular ATP release predominantly mediates Ca(2+) communication locally in highly organised, stellate-Like patterned networks of adult human astrocytes
title_short Extracellular ATP release predominantly mediates Ca(2+) communication locally in highly organised, stellate-Like patterned networks of adult human astrocytes
title_sort extracellular atp release predominantly mediates ca(2+) communication locally in highly organised, stellate-like patterned networks of adult human astrocytes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10547170/
https://www.ncbi.nlm.nih.gov/pubmed/37788259
http://dx.doi.org/10.1371/journal.pone.0289350
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