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CO(2)-Sensitive Connexin Hemichannels in Neurons and Glia: Three Different Modes of Signalling?

Connexins can assemble into either gap junctions (between two cells) or hemichannels (from one cell to the extracellular space) and mediate cell-to-cell signalling. A subset of connexins (Cx26, Cx30, Cx32) are directly sensitive to CO(2) and fluctuations in the level within a physiological range aff...

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Autores principales: Hill, Emily, Dale, Nicholas, Wall, Mark J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8304244/
https://www.ncbi.nlm.nih.gov/pubmed/34298872
http://dx.doi.org/10.3390/ijms22147254
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author Hill, Emily
Dale, Nicholas
Wall, Mark J.
author_facet Hill, Emily
Dale, Nicholas
Wall, Mark J.
author_sort Hill, Emily
collection PubMed
description Connexins can assemble into either gap junctions (between two cells) or hemichannels (from one cell to the extracellular space) and mediate cell-to-cell signalling. A subset of connexins (Cx26, Cx30, Cx32) are directly sensitive to CO(2) and fluctuations in the level within a physiological range affect their open probability, and thus, change cell conductance. These connexins are primarily found on astrocytes or oligodendrocytes, where increased CO(2) leads to ATP release, which acts on P2X and P2Y receptors of neighbouring neurons and changes excitability. CO(2)-sensitive hemichannels are also found on developing cortical neurons, where they play a role in producing spontaneous neuronal activity. It is plausible that the transient opening of hemichannels allows cation influx, leading to depolarisation. Recently, we have shown that dopaminergic neurons in the substantia nigra and GABAergic neurons in the VTA also express Cx26 hemichannels. An increase in the level of CO(2) results in hemichannel opening, increasing whole-cell conductance, and decreasing neuronal excitability. We found that the expression of Cx26 in the dopaminergic neurons in the substantia nigra at P7-10 is transferred to glial cells by P17-21, displaying a shift from being inhibitory (to neuronal activity) in young mice, to potentially excitatory (via ATP release). Thus, Cx26 hemichannels could have three modes of signalling (release of ATP, excitatory flickering open and shut and inhibitory shunting) depending on where they are expressed (neurons or glia) and the stage of development.
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spelling pubmed-83042442021-07-25 CO(2)-Sensitive Connexin Hemichannels in Neurons and Glia: Three Different Modes of Signalling? Hill, Emily Dale, Nicholas Wall, Mark J. Int J Mol Sci Review Connexins can assemble into either gap junctions (between two cells) or hemichannels (from one cell to the extracellular space) and mediate cell-to-cell signalling. A subset of connexins (Cx26, Cx30, Cx32) are directly sensitive to CO(2) and fluctuations in the level within a physiological range affect their open probability, and thus, change cell conductance. These connexins are primarily found on astrocytes or oligodendrocytes, where increased CO(2) leads to ATP release, which acts on P2X and P2Y receptors of neighbouring neurons and changes excitability. CO(2)-sensitive hemichannels are also found on developing cortical neurons, where they play a role in producing spontaneous neuronal activity. It is plausible that the transient opening of hemichannels allows cation influx, leading to depolarisation. Recently, we have shown that dopaminergic neurons in the substantia nigra and GABAergic neurons in the VTA also express Cx26 hemichannels. An increase in the level of CO(2) results in hemichannel opening, increasing whole-cell conductance, and decreasing neuronal excitability. We found that the expression of Cx26 in the dopaminergic neurons in the substantia nigra at P7-10 is transferred to glial cells by P17-21, displaying a shift from being inhibitory (to neuronal activity) in young mice, to potentially excitatory (via ATP release). Thus, Cx26 hemichannels could have three modes of signalling (release of ATP, excitatory flickering open and shut and inhibitory shunting) depending on where they are expressed (neurons or glia) and the stage of development. MDPI 2021-07-06 /pmc/articles/PMC8304244/ /pubmed/34298872 http://dx.doi.org/10.3390/ijms22147254 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Hill, Emily
Dale, Nicholas
Wall, Mark J.
CO(2)-Sensitive Connexin Hemichannels in Neurons and Glia: Three Different Modes of Signalling?
title CO(2)-Sensitive Connexin Hemichannels in Neurons and Glia: Three Different Modes of Signalling?
title_full CO(2)-Sensitive Connexin Hemichannels in Neurons and Glia: Three Different Modes of Signalling?
title_fullStr CO(2)-Sensitive Connexin Hemichannels in Neurons and Glia: Three Different Modes of Signalling?
title_full_unstemmed CO(2)-Sensitive Connexin Hemichannels in Neurons and Glia: Three Different Modes of Signalling?
title_short CO(2)-Sensitive Connexin Hemichannels in Neurons and Glia: Three Different Modes of Signalling?
title_sort co(2)-sensitive connexin hemichannels in neurons and glia: three different modes of signalling?
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8304244/
https://www.ncbi.nlm.nih.gov/pubmed/34298872
http://dx.doi.org/10.3390/ijms22147254
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