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Astrocytes regulate brain extracellular pH via a neuronal activity-dependent bicarbonate shuttle

Brain cells continuously produce and release protons into the extracellular space, with the rate of acid production corresponding to the levels of neuronal activity and metabolism. Efficient buffering and removal of excess H(+) is essential for brain function, not least because all the electrogenic...

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Autores principales: Theparambil, Shefeeq M., Hosford, Patrick S., Ruminot, Iván, Kopach, Olga, Reynolds, James R., Sandoval, Pamela Y., Rusakov, Dmitri A., Barros, L. Felipe, Gourine, Alexander V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7545092/
https://www.ncbi.nlm.nih.gov/pubmed/33033238
http://dx.doi.org/10.1038/s41467-020-18756-3
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author Theparambil, Shefeeq M.
Hosford, Patrick S.
Ruminot, Iván
Kopach, Olga
Reynolds, James R.
Sandoval, Pamela Y.
Rusakov, Dmitri A.
Barros, L. Felipe
Gourine, Alexander V.
author_facet Theparambil, Shefeeq M.
Hosford, Patrick S.
Ruminot, Iván
Kopach, Olga
Reynolds, James R.
Sandoval, Pamela Y.
Rusakov, Dmitri A.
Barros, L. Felipe
Gourine, Alexander V.
author_sort Theparambil, Shefeeq M.
collection PubMed
description Brain cells continuously produce and release protons into the extracellular space, with the rate of acid production corresponding to the levels of neuronal activity and metabolism. Efficient buffering and removal of excess H(+) is essential for brain function, not least because all the electrogenic and biochemical machinery of synaptic transmission is highly sensitive to changes in pH. Here, we describe an astroglial mechanism that contributes to the protection of the brain milieu from acidification. In vivo and in vitro experiments conducted in rodent models show that at least one third of all astrocytes release bicarbonate to buffer extracellular H(+) loads associated with increases in neuronal activity. The underlying signalling mechanism involves activity-dependent release of ATP triggering bicarbonate secretion by astrocytes via activation of metabotropic P2Y(1) receptors, recruitment of phospholipase C, release of Ca(2+) from the internal stores, and facilitated outward HCO(3)(−) transport by the electrogenic sodium bicarbonate cotransporter 1, NBCe1. These results show that astrocytes maintain local brain extracellular pH homeostasis via a neuronal activity-dependent release of bicarbonate. The data provide evidence of another important metabolic housekeeping function of these glial cells.
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spelling pubmed-75450922020-10-19 Astrocytes regulate brain extracellular pH via a neuronal activity-dependent bicarbonate shuttle Theparambil, Shefeeq M. Hosford, Patrick S. Ruminot, Iván Kopach, Olga Reynolds, James R. Sandoval, Pamela Y. Rusakov, Dmitri A. Barros, L. Felipe Gourine, Alexander V. Nat Commun Article Brain cells continuously produce and release protons into the extracellular space, with the rate of acid production corresponding to the levels of neuronal activity and metabolism. Efficient buffering and removal of excess H(+) is essential for brain function, not least because all the electrogenic and biochemical machinery of synaptic transmission is highly sensitive to changes in pH. Here, we describe an astroglial mechanism that contributes to the protection of the brain milieu from acidification. In vivo and in vitro experiments conducted in rodent models show that at least one third of all astrocytes release bicarbonate to buffer extracellular H(+) loads associated with increases in neuronal activity. The underlying signalling mechanism involves activity-dependent release of ATP triggering bicarbonate secretion by astrocytes via activation of metabotropic P2Y(1) receptors, recruitment of phospholipase C, release of Ca(2+) from the internal stores, and facilitated outward HCO(3)(−) transport by the electrogenic sodium bicarbonate cotransporter 1, NBCe1. These results show that astrocytes maintain local brain extracellular pH homeostasis via a neuronal activity-dependent release of bicarbonate. The data provide evidence of another important metabolic housekeeping function of these glial cells. Nature Publishing Group UK 2020-10-08 /pmc/articles/PMC7545092/ /pubmed/33033238 http://dx.doi.org/10.1038/s41467-020-18756-3 Text en © The Author(s) 2020 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
Theparambil, Shefeeq M.
Hosford, Patrick S.
Ruminot, Iván
Kopach, Olga
Reynolds, James R.
Sandoval, Pamela Y.
Rusakov, Dmitri A.
Barros, L. Felipe
Gourine, Alexander V.
Astrocytes regulate brain extracellular pH via a neuronal activity-dependent bicarbonate shuttle
title Astrocytes regulate brain extracellular pH via a neuronal activity-dependent bicarbonate shuttle
title_full Astrocytes regulate brain extracellular pH via a neuronal activity-dependent bicarbonate shuttle
title_fullStr Astrocytes regulate brain extracellular pH via a neuronal activity-dependent bicarbonate shuttle
title_full_unstemmed Astrocytes regulate brain extracellular pH via a neuronal activity-dependent bicarbonate shuttle
title_short Astrocytes regulate brain extracellular pH via a neuronal activity-dependent bicarbonate shuttle
title_sort astrocytes regulate brain extracellular ph via a neuronal activity-dependent bicarbonate shuttle
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7545092/
https://www.ncbi.nlm.nih.gov/pubmed/33033238
http://dx.doi.org/10.1038/s41467-020-18756-3
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