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A Highly Temperature-sensitive Proton Current in Mouse Bone Marrow–derived Mast Cells

Proton (H(+)) conductive pathways are suggested to play roles in the regulation of intracellular pH. We characterized temperature-sensitive whole cell currents in mouse bone marrow–derived mast cells (BMMC), immature proliferating mast cells generated by in vitro culture. Heating from 24 to 36°C rev...

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Detalles Bibliográficos
Autores principales: Kuno, Miyuki, Kawawaki, Junko, Nakamura, Fusao
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1997
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2217037/
https://www.ncbi.nlm.nih.gov/pubmed/9222899
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author Kuno, Miyuki
Kawawaki, Junko
Nakamura, Fusao
author_facet Kuno, Miyuki
Kawawaki, Junko
Nakamura, Fusao
author_sort Kuno, Miyuki
collection PubMed
description Proton (H(+)) conductive pathways are suggested to play roles in the regulation of intracellular pH. We characterized temperature-sensitive whole cell currents in mouse bone marrow–derived mast cells (BMMC), immature proliferating mast cells generated by in vitro culture. Heating from 24 to 36°C reversibly and repeatedly activated a voltage-dependent outward conductance with Q(10) of 9.9 ± 3.1 (mean ± SD) (n = 6). Either a decrease in intracellular pH or an increase in extracellular pH enhanced the amplitude and shifted the activation voltage to more negative potentials. With acidic intracellular solutions (pH 5.5), the outward current was detected in some cells at 24°C and Q(10) was 6.0 ± 2.6 (n = 9). The reversal potential was unaffected by changes in concentrations of major ionic constituents (K(+), Cl(−), and Na(+)), but depended on the pH gradient, suggesting that H(+) (equivalents) is a major ion species carrying the current. The H(+) current was featured by slow activation kinetics upon membrane depolarization, and the activation time course was accelerated by increases in depolarization, elevating temperature and extracellular alkalization. The current was recorded even when ATP was removed from the intracellular solution, but the mean amplitude was smaller than that in the presence of ATP. The H(+) current was reversibly inhibited by Zn(2+) but not by bafilomycin A(1), an inhibitor for a vacuolar type H(+)-ATPase. Macroscopic measurements of pH using a fluorescent dye (BCECF) revealed that a rapid recovery of intracellular pH from acid-load was attenuated by lowering temperature, addition of Zn(2+), and depletion of extracellular K(+), but not by bafilomycin A(1). These results suggest that the H(+) conductive pathway contributes to intracellular pH homeostasis of BMMC and that the high activation energy may be involved in enhancement of the H(+) conductance.
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spelling pubmed-22170372008-04-22 A Highly Temperature-sensitive Proton Current in Mouse Bone Marrow–derived Mast Cells Kuno, Miyuki Kawawaki, Junko Nakamura, Fusao J Gen Physiol Article Proton (H(+)) conductive pathways are suggested to play roles in the regulation of intracellular pH. We characterized temperature-sensitive whole cell currents in mouse bone marrow–derived mast cells (BMMC), immature proliferating mast cells generated by in vitro culture. Heating from 24 to 36°C reversibly and repeatedly activated a voltage-dependent outward conductance with Q(10) of 9.9 ± 3.1 (mean ± SD) (n = 6). Either a decrease in intracellular pH or an increase in extracellular pH enhanced the amplitude and shifted the activation voltage to more negative potentials. With acidic intracellular solutions (pH 5.5), the outward current was detected in some cells at 24°C and Q(10) was 6.0 ± 2.6 (n = 9). The reversal potential was unaffected by changes in concentrations of major ionic constituents (K(+), Cl(−), and Na(+)), but depended on the pH gradient, suggesting that H(+) (equivalents) is a major ion species carrying the current. The H(+) current was featured by slow activation kinetics upon membrane depolarization, and the activation time course was accelerated by increases in depolarization, elevating temperature and extracellular alkalization. The current was recorded even when ATP was removed from the intracellular solution, but the mean amplitude was smaller than that in the presence of ATP. The H(+) current was reversibly inhibited by Zn(2+) but not by bafilomycin A(1), an inhibitor for a vacuolar type H(+)-ATPase. Macroscopic measurements of pH using a fluorescent dye (BCECF) revealed that a rapid recovery of intracellular pH from acid-load was attenuated by lowering temperature, addition of Zn(2+), and depletion of extracellular K(+), but not by bafilomycin A(1). These results suggest that the H(+) conductive pathway contributes to intracellular pH homeostasis of BMMC and that the high activation energy may be involved in enhancement of the H(+) conductance. The Rockefeller University Press 1997-06-01 /pmc/articles/PMC2217037/ /pubmed/9222899 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Kuno, Miyuki
Kawawaki, Junko
Nakamura, Fusao
A Highly Temperature-sensitive Proton Current in Mouse Bone Marrow–derived Mast Cells
title A Highly Temperature-sensitive Proton Current in Mouse Bone Marrow–derived Mast Cells
title_full A Highly Temperature-sensitive Proton Current in Mouse Bone Marrow–derived Mast Cells
title_fullStr A Highly Temperature-sensitive Proton Current in Mouse Bone Marrow–derived Mast Cells
title_full_unstemmed A Highly Temperature-sensitive Proton Current in Mouse Bone Marrow–derived Mast Cells
title_short A Highly Temperature-sensitive Proton Current in Mouse Bone Marrow–derived Mast Cells
title_sort highly temperature-sensitive proton current in mouse bone marrow–derived mast cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2217037/
https://www.ncbi.nlm.nih.gov/pubmed/9222899
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