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The contribution of TWIK-1 channels to astrocyte K(+) current is limited by retention in intracellular compartments

TWIK-1 two-pore domain K(+) channels are expressed abundantly in astrocytes. In the present study, we examined the extent to which TWIK-1 contributes to the linear current-voltage (I–V) relationship (passive) K(+) membrane conductance, a dominant electrophysiological feature of mature hippocampal as...

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Autores principales: Wang, Wei, Putra, Adhytia, Schools, Gary P., Ma, Baofeng, Chen, Haijun, Kaczmarek, Leonard K., Barhanin, Jacques, Lesage, Florian, Zhou, Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3856854/
https://www.ncbi.nlm.nih.gov/pubmed/24368895
http://dx.doi.org/10.3389/fncel.2013.00246
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author Wang, Wei
Putra, Adhytia
Schools, Gary P.
Ma, Baofeng
Chen, Haijun
Kaczmarek, Leonard K.
Barhanin, Jacques
Lesage, Florian
Zhou, Min
author_facet Wang, Wei
Putra, Adhytia
Schools, Gary P.
Ma, Baofeng
Chen, Haijun
Kaczmarek, Leonard K.
Barhanin, Jacques
Lesage, Florian
Zhou, Min
author_sort Wang, Wei
collection PubMed
description TWIK-1 two-pore domain K(+) channels are expressed abundantly in astrocytes. In the present study, we examined the extent to which TWIK-1 contributes to the linear current-voltage (I–V) relationship (passive) K(+) membrane conductance, a dominant electrophysiological feature of mature hippocampal astrocytes. Astrocytes from TWIK-1 knockout mice have a more negative resting potential than those from wild type animals and a reduction in both inward rectification and Cs(+) permeability. Nevertheless, the overall whole-cell passive conductance is not altered significantly in TWIK-1 knockout astrocytes. The expression of K(ir)4.1 and TREK-1, two other major astrocytic K(+) channels, or of other two-pore K(+) channels is not altered in TWIK-1 knockout mice, suggesting that the mild effect of TWIK-1 knockout does not result from compensation by these channels. Fractionation experiments showed that TWIK-1 is primarily localized in intracellular cytoplasmic fractions (55%) and mildly hydrophobic internal compartment fractions (41%), with only 5% in fractions containing plasma membranes. Our study revealed that TWIK-1 proteins are mainly located in the intracellular compartments of hippocampal astrocyte under physiological condition, therefore a minimal contribution of TWIK-1 channels to whole-cell currents is likely attributable to a relatively low level presence of channels in the plasma membrane.
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spelling pubmed-38568542013-12-24 The contribution of TWIK-1 channels to astrocyte K(+) current is limited by retention in intracellular compartments Wang, Wei Putra, Adhytia Schools, Gary P. Ma, Baofeng Chen, Haijun Kaczmarek, Leonard K. Barhanin, Jacques Lesage, Florian Zhou, Min Front Cell Neurosci Neuroscience TWIK-1 two-pore domain K(+) channels are expressed abundantly in astrocytes. In the present study, we examined the extent to which TWIK-1 contributes to the linear current-voltage (I–V) relationship (passive) K(+) membrane conductance, a dominant electrophysiological feature of mature hippocampal astrocytes. Astrocytes from TWIK-1 knockout mice have a more negative resting potential than those from wild type animals and a reduction in both inward rectification and Cs(+) permeability. Nevertheless, the overall whole-cell passive conductance is not altered significantly in TWIK-1 knockout astrocytes. The expression of K(ir)4.1 and TREK-1, two other major astrocytic K(+) channels, or of other two-pore K(+) channels is not altered in TWIK-1 knockout mice, suggesting that the mild effect of TWIK-1 knockout does not result from compensation by these channels. Fractionation experiments showed that TWIK-1 is primarily localized in intracellular cytoplasmic fractions (55%) and mildly hydrophobic internal compartment fractions (41%), with only 5% in fractions containing plasma membranes. Our study revealed that TWIK-1 proteins are mainly located in the intracellular compartments of hippocampal astrocyte under physiological condition, therefore a minimal contribution of TWIK-1 channels to whole-cell currents is likely attributable to a relatively low level presence of channels in the plasma membrane. Frontiers Media S.A. 2013-12-09 /pmc/articles/PMC3856854/ /pubmed/24368895 http://dx.doi.org/10.3389/fncel.2013.00246 Text en Copyright © 2013 Wang, Putra, Schools, Ma, Chen, Kaczmarek, Barhanin, Lesage and Zhou. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Wang, Wei
Putra, Adhytia
Schools, Gary P.
Ma, Baofeng
Chen, Haijun
Kaczmarek, Leonard K.
Barhanin, Jacques
Lesage, Florian
Zhou, Min
The contribution of TWIK-1 channels to astrocyte K(+) current is limited by retention in intracellular compartments
title The contribution of TWIK-1 channels to astrocyte K(+) current is limited by retention in intracellular compartments
title_full The contribution of TWIK-1 channels to astrocyte K(+) current is limited by retention in intracellular compartments
title_fullStr The contribution of TWIK-1 channels to astrocyte K(+) current is limited by retention in intracellular compartments
title_full_unstemmed The contribution of TWIK-1 channels to astrocyte K(+) current is limited by retention in intracellular compartments
title_short The contribution of TWIK-1 channels to astrocyte K(+) current is limited by retention in intracellular compartments
title_sort contribution of twik-1 channels to astrocyte k(+) current is limited by retention in intracellular compartments
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3856854/
https://www.ncbi.nlm.nih.gov/pubmed/24368895
http://dx.doi.org/10.3389/fncel.2013.00246
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