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Intracellular spermine prevents acid-induced uncoupling of Cx43 gap junction channels

Polyamines (PAs), such as spermine and spermidine, modulate the activity of numerous receptors and channels in the central nervous system (CNS) and are stored in glial cells; however, little attention has been paid to their role in the regulation of connexin (Cx)-based gap junction channels. We have...

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Autores principales: Skatchkov, Serguei N., Bukauskas, Feliksas F., Benedikt, Jan, Inyushin, Mikhail, Kucheryavykh, Yuriy V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4493885/
https://www.ncbi.nlm.nih.gov/pubmed/26011388
http://dx.doi.org/10.1097/WNR.0000000000000385
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author Skatchkov, Serguei N.
Bukauskas, Feliksas F.
Benedikt, Jan
Inyushin, Mikhail
Kucheryavykh, Yuriy V.
author_facet Skatchkov, Serguei N.
Bukauskas, Feliksas F.
Benedikt, Jan
Inyushin, Mikhail
Kucheryavykh, Yuriy V.
author_sort Skatchkov, Serguei N.
collection PubMed
description Polyamines (PAs), such as spermine and spermidine, modulate the activity of numerous receptors and channels in the central nervous system (CNS) and are stored in glial cells; however, little attention has been paid to their role in the regulation of connexin (Cx)-based gap junction channels. We have previously shown that PAs facilitate diffusion of Lucifer Yellow through astrocytic gap junctions in acute brain slices; therefore, we hypothesized that spermine can regulate Cx43-mediated (as the most abundant Cx in astrocytes) gap junctional communication. We used electrophysiological patch-clamp recording from paired Novikoff cells endogenously expressing Cx43 and HeLaCx43-EGFP transfectants to study pH-dependent modulation of cell–cell coupling in the presence or absence of PAs. Our results showed (i) a higher increase in gap junctional communication at higher concentrations of cytoplasmic spermine, and (ii) that spermine prevented uncoupling of gap junctions at low intracellular pH. Taken together, we conclude that spermine enhances Cx43-mediated gap junctional communication and may preserve neuronal excitability during ischemia and trauma when pH in the brain acidifies. We, therefore, suggest a new role of spermine in the regulation of a Cx43-based network under (patho)physiological conditions.
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spelling pubmed-44938852015-07-17 Intracellular spermine prevents acid-induced uncoupling of Cx43 gap junction channels Skatchkov, Serguei N. Bukauskas, Feliksas F. Benedikt, Jan Inyushin, Mikhail Kucheryavykh, Yuriy V. Neuroreport Cellular, Molecular and Developmental Neuroscience Polyamines (PAs), such as spermine and spermidine, modulate the activity of numerous receptors and channels in the central nervous system (CNS) and are stored in glial cells; however, little attention has been paid to their role in the regulation of connexin (Cx)-based gap junction channels. We have previously shown that PAs facilitate diffusion of Lucifer Yellow through astrocytic gap junctions in acute brain slices; therefore, we hypothesized that spermine can regulate Cx43-mediated (as the most abundant Cx in astrocytes) gap junctional communication. We used electrophysiological patch-clamp recording from paired Novikoff cells endogenously expressing Cx43 and HeLaCx43-EGFP transfectants to study pH-dependent modulation of cell–cell coupling in the presence or absence of PAs. Our results showed (i) a higher increase in gap junctional communication at higher concentrations of cytoplasmic spermine, and (ii) that spermine prevented uncoupling of gap junctions at low intracellular pH. Taken together, we conclude that spermine enhances Cx43-mediated gap junctional communication and may preserve neuronal excitability during ischemia and trauma when pH in the brain acidifies. We, therefore, suggest a new role of spermine in the regulation of a Cx43-based network under (patho)physiological conditions. Lippincott Williams & Wilkins 2015-06-17 2015-06-03 /pmc/articles/PMC4493885/ /pubmed/26011388 http://dx.doi.org/10.1097/WNR.0000000000000385 Text en Copyright © 2015 Wolters Kluwer Health, Inc. All rights reserved. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially. http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Cellular, Molecular and Developmental Neuroscience
Skatchkov, Serguei N.
Bukauskas, Feliksas F.
Benedikt, Jan
Inyushin, Mikhail
Kucheryavykh, Yuriy V.
Intracellular spermine prevents acid-induced uncoupling of Cx43 gap junction channels
title Intracellular spermine prevents acid-induced uncoupling of Cx43 gap junction channels
title_full Intracellular spermine prevents acid-induced uncoupling of Cx43 gap junction channels
title_fullStr Intracellular spermine prevents acid-induced uncoupling of Cx43 gap junction channels
title_full_unstemmed Intracellular spermine prevents acid-induced uncoupling of Cx43 gap junction channels
title_short Intracellular spermine prevents acid-induced uncoupling of Cx43 gap junction channels
title_sort intracellular spermine prevents acid-induced uncoupling of cx43 gap junction channels
topic Cellular, Molecular and Developmental Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4493885/
https://www.ncbi.nlm.nih.gov/pubmed/26011388
http://dx.doi.org/10.1097/WNR.0000000000000385
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