Menthol increases human glioblastoma intracellular Ca<sup>2+</sup>, BK channel activity and cell migration

<p>Abstract</p> <p>This study examined the effect of menthol, an agonist for transient receptor potential melastatin 8 (TRPM8) ion channels, to increase intracellular Ca<sup>2+ </sup>concentration, [Ca<sup>2+</sup>]<sub>i</sub>, in human glioblas...

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Main Authors: Bartley Jeremy W, Wondergem Robert
Format: Article
Language:English
Published: BMC 2009-09-01
Series:Journal of Biomedical Science
Online Access:http://www.jbiomedsci.com/content/16/1/90
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spelling doaj-bbb9cc4eb6924bfa8709776759caf9262020-11-25T02:18:57ZengBMCJournal of Biomedical Science1021-77701423-01272009-09-011619010.1186/1423-0127-16-90Menthol increases human glioblastoma intracellular Ca<sup>2+</sup>, BK channel activity and cell migrationBartley Jeremy WWondergem Robert<p>Abstract</p> <p>This study examined the effect of menthol, an agonist for transient receptor potential melastatin 8 (TRPM8) ion channels, to increase intracellular Ca<sup>2+ </sup>concentration, [Ca<sup>2+</sup>]<sub>i</sub>, in human glioblastoma cells (DBTRG cells), which resulted in activation of the large-conductance Ca<sup>2+</sup>-activated K<sup>+ </sup>membrane ion channels (BK channels). Voltage ramps applied over 300 ms from -100 to 100 mV resulted in membrane currents with marked inwardly- and outwardly-rectifying components. Paxilline (2 μM) abolished the outwardly-rectifying current. Outwardly-rectifying on-cell patch currents were increased markedly by menthol (100 μM) added to the bath. The estimated on-cell conductance of these channels was 253 pS. Kinetic analysis showed that added menthol increased channel open probability and mean open frequency after 5 min. In a similar time course menthol increased [Ca<sup>2+</sup>]<sub>i</sub>, and this increase was abolished either by added paxilline, tetraethylammonium ion or by Ca<sup>2+</sup>-free external solution. Finally, menthol stimulated the rate of DBTRG cell migration into scratch wounds made in confluent cells, and this also was inhibited by paxilline or by tetraethylammonium ion. We conclude that menthol, a TRPM8 agonist, increases DBTRG cell [Ca<sup>2+</sup>]<sub>i </sub>that in turn activates membrane BK ion channels. Inhibition of BK channels by paxilline reverses menthol-stimulated increase of [Ca<sup>2+</sup>]<sub>i </sub>and of cell migration. Thus, BK channels function to maintain elevations in [Ca<sup>2+</sup>]<sub>i </sub>needed to sustain increases in DBTRG cell migration.</p> http://www.jbiomedsci.com/content/16/1/90
collection DOAJ
language English
format Article
sources DOAJ
author Bartley Jeremy W
Wondergem Robert
spellingShingle Bartley Jeremy W
Wondergem Robert
Menthol increases human glioblastoma intracellular Ca<sup>2+</sup>, BK channel activity and cell migration
Journal of Biomedical Science
author_facet Bartley Jeremy W
Wondergem Robert
author_sort Bartley Jeremy W
title Menthol increases human glioblastoma intracellular Ca<sup>2+</sup>, BK channel activity and cell migration
title_short Menthol increases human glioblastoma intracellular Ca<sup>2+</sup>, BK channel activity and cell migration
title_full Menthol increases human glioblastoma intracellular Ca<sup>2+</sup>, BK channel activity and cell migration
title_fullStr Menthol increases human glioblastoma intracellular Ca<sup>2+</sup>, BK channel activity and cell migration
title_full_unstemmed Menthol increases human glioblastoma intracellular Ca<sup>2+</sup>, BK channel activity and cell migration
title_sort menthol increases human glioblastoma intracellular ca<sup>2+</sup>, bk channel activity and cell migration
publisher BMC
series Journal of Biomedical Science
issn 1021-7770
1423-0127
publishDate 2009-09-01
description <p>Abstract</p> <p>This study examined the effect of menthol, an agonist for transient receptor potential melastatin 8 (TRPM8) ion channels, to increase intracellular Ca<sup>2+ </sup>concentration, [Ca<sup>2+</sup>]<sub>i</sub>, in human glioblastoma cells (DBTRG cells), which resulted in activation of the large-conductance Ca<sup>2+</sup>-activated K<sup>+ </sup>membrane ion channels (BK channels). Voltage ramps applied over 300 ms from -100 to 100 mV resulted in membrane currents with marked inwardly- and outwardly-rectifying components. Paxilline (2 μM) abolished the outwardly-rectifying current. Outwardly-rectifying on-cell patch currents were increased markedly by menthol (100 μM) added to the bath. The estimated on-cell conductance of these channels was 253 pS. Kinetic analysis showed that added menthol increased channel open probability and mean open frequency after 5 min. In a similar time course menthol increased [Ca<sup>2+</sup>]<sub>i</sub>, and this increase was abolished either by added paxilline, tetraethylammonium ion or by Ca<sup>2+</sup>-free external solution. Finally, menthol stimulated the rate of DBTRG cell migration into scratch wounds made in confluent cells, and this also was inhibited by paxilline or by tetraethylammonium ion. We conclude that menthol, a TRPM8 agonist, increases DBTRG cell [Ca<sup>2+</sup>]<sub>i </sub>that in turn activates membrane BK ion channels. Inhibition of BK channels by paxilline reverses menthol-stimulated increase of [Ca<sup>2+</sup>]<sub>i </sub>and of cell migration. Thus, BK channels function to maintain elevations in [Ca<sup>2+</sup>]<sub>i </sub>needed to sustain increases in DBTRG cell migration.</p>
url http://www.jbiomedsci.com/content/16/1/90
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AT wondergemrobert mentholincreaseshumanglioblastomaintracellularcasup2supbkchannelactivityandcellmigration
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