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Modeling the Contributions of Ca(2+) Flows to Spontaneous Ca(2+) Oscillations and Cortical Spreading Depression-Triggered Ca(2+) Waves in Astrocyte Networks

Astrocytes participate in brain functions through Ca(2+) signals, including Ca(2+) waves and Ca(2+) oscillations. Currently the mechanisms of Ca(2+) signals in astrocytes are not fully clear. Here, we present a computational model to specify the relative contributions of different Ca(2+) flows betwe...

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Autores principales: Li, Bing, Chen, Shangbin, Zeng, Shaoqun, Luo, Qingming, Li, Pengcheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3485305/
https://www.ncbi.nlm.nih.gov/pubmed/23119049
http://dx.doi.org/10.1371/journal.pone.0048534
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author Li, Bing
Chen, Shangbin
Zeng, Shaoqun
Luo, Qingming
Li, Pengcheng
author_facet Li, Bing
Chen, Shangbin
Zeng, Shaoqun
Luo, Qingming
Li, Pengcheng
author_sort Li, Bing
collection PubMed
description Astrocytes participate in brain functions through Ca(2+) signals, including Ca(2+) waves and Ca(2+) oscillations. Currently the mechanisms of Ca(2+) signals in astrocytes are not fully clear. Here, we present a computational model to specify the relative contributions of different Ca(2+) flows between the extracellular space, the cytoplasm and the endoplasmic reticulum of astrocytes to the generation of spontaneous Ca(2+) oscillations (CASs) and cortical spreading depression (CSD)-triggered Ca(2+) waves (CSDCWs) in a one-dimensional astrocyte network. This model shows that CASs depend primarily on Ca(2+) released from internal stores of astrocytes, and CSDCWs depend mainly on voltage-gated Ca(2+) influx. It predicts that voltage-gated Ca(2+) influx is able to generate Ca(2+) waves during the process of CSD even after depleting internal Ca(2+) stores. Furthermore, the model investigates the interactions between CASs and CSDCWs and shows that the pass of CSDCWs suppresses CASs, whereas CASs do not prevent the generation of CSDCWs. This work quantitatively analyzes the generation of astrocytic Ca(2+) signals and indicates different mechanisms underlying CSDCWs and non-CSDCWs. Research on the different types of Ca(2+) signals might help to understand the ways by which astrocytes participate in information processing in brain functions.
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spelling pubmed-34853052012-11-01 Modeling the Contributions of Ca(2+) Flows to Spontaneous Ca(2+) Oscillations and Cortical Spreading Depression-Triggered Ca(2+) Waves in Astrocyte Networks Li, Bing Chen, Shangbin Zeng, Shaoqun Luo, Qingming Li, Pengcheng PLoS One Research Article Astrocytes participate in brain functions through Ca(2+) signals, including Ca(2+) waves and Ca(2+) oscillations. Currently the mechanisms of Ca(2+) signals in astrocytes are not fully clear. Here, we present a computational model to specify the relative contributions of different Ca(2+) flows between the extracellular space, the cytoplasm and the endoplasmic reticulum of astrocytes to the generation of spontaneous Ca(2+) oscillations (CASs) and cortical spreading depression (CSD)-triggered Ca(2+) waves (CSDCWs) in a one-dimensional astrocyte network. This model shows that CASs depend primarily on Ca(2+) released from internal stores of astrocytes, and CSDCWs depend mainly on voltage-gated Ca(2+) influx. It predicts that voltage-gated Ca(2+) influx is able to generate Ca(2+) waves during the process of CSD even after depleting internal Ca(2+) stores. Furthermore, the model investigates the interactions between CASs and CSDCWs and shows that the pass of CSDCWs suppresses CASs, whereas CASs do not prevent the generation of CSDCWs. This work quantitatively analyzes the generation of astrocytic Ca(2+) signals and indicates different mechanisms underlying CSDCWs and non-CSDCWs. Research on the different types of Ca(2+) signals might help to understand the ways by which astrocytes participate in information processing in brain functions. Public Library of Science 2012-10-31 /pmc/articles/PMC3485305/ /pubmed/23119049 http://dx.doi.org/10.1371/journal.pone.0048534 Text en © 2012 Li et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Li, Bing
Chen, Shangbin
Zeng, Shaoqun
Luo, Qingming
Li, Pengcheng
Modeling the Contributions of Ca(2+) Flows to Spontaneous Ca(2+) Oscillations and Cortical Spreading Depression-Triggered Ca(2+) Waves in Astrocyte Networks
title Modeling the Contributions of Ca(2+) Flows to Spontaneous Ca(2+) Oscillations and Cortical Spreading Depression-Triggered Ca(2+) Waves in Astrocyte Networks
title_full Modeling the Contributions of Ca(2+) Flows to Spontaneous Ca(2+) Oscillations and Cortical Spreading Depression-Triggered Ca(2+) Waves in Astrocyte Networks
title_fullStr Modeling the Contributions of Ca(2+) Flows to Spontaneous Ca(2+) Oscillations and Cortical Spreading Depression-Triggered Ca(2+) Waves in Astrocyte Networks
title_full_unstemmed Modeling the Contributions of Ca(2+) Flows to Spontaneous Ca(2+) Oscillations and Cortical Spreading Depression-Triggered Ca(2+) Waves in Astrocyte Networks
title_short Modeling the Contributions of Ca(2+) Flows to Spontaneous Ca(2+) Oscillations and Cortical Spreading Depression-Triggered Ca(2+) Waves in Astrocyte Networks
title_sort modeling the contributions of ca(2+) flows to spontaneous ca(2+) oscillations and cortical spreading depression-triggered ca(2+) waves in astrocyte networks
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3485305/
https://www.ncbi.nlm.nih.gov/pubmed/23119049
http://dx.doi.org/10.1371/journal.pone.0048534
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