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Disentangling astroglial physiology with a realistic cell model in silico
Electrically non-excitable astroglia take up neurotransmitters, buffer extracellular K(+) and generate Ca(2+) signals that release molecular regulators of neural circuitry. The underlying machinery remains enigmatic, mainly because the sponge-like astrocyte morphology has been difficult to access ex...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6120909/ https://www.ncbi.nlm.nih.gov/pubmed/30177844 http://dx.doi.org/10.1038/s41467-018-05896-w |
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author | Savtchenko, Leonid P. Bard, Lucie Jensen, Thomas P. Reynolds, James P. Kraev, Igor Medvedev, Nikolay Stewart, Michael G. Henneberger, Christian Rusakov, Dmitri A. |
author_facet | Savtchenko, Leonid P. Bard, Lucie Jensen, Thomas P. Reynolds, James P. Kraev, Igor Medvedev, Nikolay Stewart, Michael G. Henneberger, Christian Rusakov, Dmitri A. |
author_sort | Savtchenko, Leonid P. |
collection | PubMed |
description | Electrically non-excitable astroglia take up neurotransmitters, buffer extracellular K(+) and generate Ca(2+) signals that release molecular regulators of neural circuitry. The underlying machinery remains enigmatic, mainly because the sponge-like astrocyte morphology has been difficult to access experimentally or explore theoretically. Here, we systematically incorporate multi-scale, tri-dimensional astroglial architecture into a realistic multi-compartmental cell model, which we constrain by empirical tests and integrate into the NEURON computational biophysical environment. This approach is implemented as a flexible astrocyte-model builder ASTRO. As a proof-of-concept, we explore an in silico astrocyte to evaluate basic cell physiology features inaccessible experimentally. Our simulations suggest that currents generated by glutamate transporters or K(+) channels have negligible distant effects on membrane voltage and that individual astrocytes can successfully handle extracellular K(+) hotspots. We show how intracellular Ca(2+) buffers affect Ca(2+) waves and why the classical Ca(2+) sparks-and-puffs mechanism is theoretically compatible with common readouts of astroglial Ca(2+) imaging. |
format | Online Article Text |
id | pubmed-6120909 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61209092018-09-05 Disentangling astroglial physiology with a realistic cell model in silico Savtchenko, Leonid P. Bard, Lucie Jensen, Thomas P. Reynolds, James P. Kraev, Igor Medvedev, Nikolay Stewart, Michael G. Henneberger, Christian Rusakov, Dmitri A. Nat Commun Article Electrically non-excitable astroglia take up neurotransmitters, buffer extracellular K(+) and generate Ca(2+) signals that release molecular regulators of neural circuitry. The underlying machinery remains enigmatic, mainly because the sponge-like astrocyte morphology has been difficult to access experimentally or explore theoretically. Here, we systematically incorporate multi-scale, tri-dimensional astroglial architecture into a realistic multi-compartmental cell model, which we constrain by empirical tests and integrate into the NEURON computational biophysical environment. This approach is implemented as a flexible astrocyte-model builder ASTRO. As a proof-of-concept, we explore an in silico astrocyte to evaluate basic cell physiology features inaccessible experimentally. Our simulations suggest that currents generated by glutamate transporters or K(+) channels have negligible distant effects on membrane voltage and that individual astrocytes can successfully handle extracellular K(+) hotspots. We show how intracellular Ca(2+) buffers affect Ca(2+) waves and why the classical Ca(2+) sparks-and-puffs mechanism is theoretically compatible with common readouts of astroglial Ca(2+) imaging. Nature Publishing Group UK 2018-09-03 /pmc/articles/PMC6120909/ /pubmed/30177844 http://dx.doi.org/10.1038/s41467-018-05896-w Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Savtchenko, Leonid P. Bard, Lucie Jensen, Thomas P. Reynolds, James P. Kraev, Igor Medvedev, Nikolay Stewart, Michael G. Henneberger, Christian Rusakov, Dmitri A. Disentangling astroglial physiology with a realistic cell model in silico |
title | Disentangling astroglial physiology with a realistic cell model in silico |
title_full | Disentangling astroglial physiology with a realistic cell model in silico |
title_fullStr | Disentangling astroglial physiology with a realistic cell model in silico |
title_full_unstemmed | Disentangling astroglial physiology with a realistic cell model in silico |
title_short | Disentangling astroglial physiology with a realistic cell model in silico |
title_sort | disentangling astroglial physiology with a realistic cell model in silico |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6120909/ https://www.ncbi.nlm.nih.gov/pubmed/30177844 http://dx.doi.org/10.1038/s41467-018-05896-w |
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