Activation of the TASK-2 channel after cell swelling is dependent on tyrosine phosphorylation

Research output: Contribution to journalJournal articlepeer-review

Standard

Activation of the TASK-2 channel after cell swelling is dependent on tyrosine phosphorylation. / Kirkegaard, Signe Skyum; Lambert, Ian Henry; Gammeltoft, Steen; Hoffmann, Else Kay.

In: American Journal of Physiology (Consolidated), Vol. 299, No. 4, 01.10.2010, p. C844-53.

Research output: Contribution to journalJournal articlepeer-review

Harvard

Kirkegaard, SS, Lambert, IH, Gammeltoft, S & Hoffmann, EK 2010, 'Activation of the TASK-2 channel after cell swelling is dependent on tyrosine phosphorylation', American Journal of Physiology (Consolidated), vol. 299, no. 4, pp. C844-53. https://doi.org/10.1152/ajpcell.00024.2010

APA

Kirkegaard, S. S., Lambert, I. H., Gammeltoft, S., & Hoffmann, E. K. (2010). Activation of the TASK-2 channel after cell swelling is dependent on tyrosine phosphorylation. American Journal of Physiology (Consolidated), 299(4), C844-53. https://doi.org/10.1152/ajpcell.00024.2010

Vancouver

Kirkegaard SS, Lambert IH, Gammeltoft S, Hoffmann EK. Activation of the TASK-2 channel after cell swelling is dependent on tyrosine phosphorylation. American Journal of Physiology (Consolidated). 2010 Oct 1;299(4):C844-53. https://doi.org/10.1152/ajpcell.00024.2010

Author

Kirkegaard, Signe Skyum ; Lambert, Ian Henry ; Gammeltoft, Steen ; Hoffmann, Else Kay. / Activation of the TASK-2 channel after cell swelling is dependent on tyrosine phosphorylation. In: American Journal of Physiology (Consolidated). 2010 ; Vol. 299, No. 4. pp. C844-53.

Bibtex

@article{24200ac03d3749c5b480df928d62edc0,
title = "Activation of the TASK-2 channel after cell swelling is dependent on tyrosine phosphorylation",
abstract = "The swelling-activated K(+) currents (I(K,vol)) in Ehrlich ascites tumor cells (EATC) has been reported to be through the two-pore domain (K(2p)), TWIK-related acid-sensitive K(+) channel 2 (TASK-2). The regulatory volume decrease (RVD), following hypotonic exposure in EATC, is rate limited by I(K,vol) indicating that inhibition of RVD reflects inhibition of TASK-2. We find that in EATC the tyrosine kinase inhibitor genistein inhibits RVD by 90%, and that the tyrosine phosphatase inhibitor monoperoxo(picolinato)-oxo-vanadate(V) [mpV(pic)] shifted the volume set point for inactivation of the channel to a lower cell volume. Swelling-activated K(+) efflux was impaired by genistein and the Src kinase family inhibitor 4-amino-5-(4-chloro-phenyl)-7-(t-butyl)pyrazolo[3,4-d]pyrimidine (PP2) and enhanced by the tyrosine phosphatase inhibitor mpV(pic). With the use of the TASK-2 inhibitor clofilium, it is demonstrated that mpV(pic) increased the volume-sensitive part of the K(+) efflux 1.3 times. To exclude K(+) efflux via a KCl cotransporter, cellular Cl(-) was substituted with NO(3)(-). Also under these conditions K(+) efflux was completely blocked by genistein. Thus tyrosine kinases seem to be involved in the activation of the volume-sensitive K(+) channel, whereas tyrosine phosphatases appears to be involved in inactivation of the channel. Overexpressing TASK-2 in human embryonic kidney (HEK)-293 cells increased the RVD rate and reduced the volume set point. TASK-2 has tyrosine sites, and precipitation of TASK-2 together with Western blotting and antibodies against phosphotyrosines revealed a cell swelling-induced, time-dependent tyrosine phosphorylation of the channel. Even though we found an inhibiting effect of PP2 on RVD, neither Src nor the focal adhesion kinase (FAK) seem to be involved. Inhibitors of the epidermal growth factor receptor tyrosine kinases had no effect on RVD, whereas the Janus kinase (JAK) inhibitor cucurbitacin inhibited the RVD by 40%. It is suggested that the cytokine receptor-coupled JAK/STAT pathway is upstream of the swelling-induced phosphorylation and activation of TASK-2 in EATC.",
keywords = "Animals, Cell Line, Cell Size, Enzyme Inhibitors, Female, Genistein, Humans, Hypotonic Solutions, Janus Kinases, Mice, Patch-Clamp Techniques, Phosphorylation, Potassium, Potassium Channels, Tandem Pore Domain, Protein-Tyrosine Kinases, STAT Transcription Factors, Signal Transduction, Tyrosine",
author = "Kirkegaard, {Signe Skyum} and Lambert, {Ian Henry} and Steen Gammeltoft and Hoffmann, {Else Kay}",
year = "2010",
month = oct,
day = "1",
doi = "10.1152/ajpcell.00024.2010",
language = "English",
volume = "299",
pages = "C844--53",
journal = "American Journal of Physiology - Cell Physiology",
issn = "0363-6143",
publisher = "American Physiological Society",
number = "4",

}

RIS

TY - JOUR

T1 - Activation of the TASK-2 channel after cell swelling is dependent on tyrosine phosphorylation

AU - Kirkegaard, Signe Skyum

AU - Lambert, Ian Henry

AU - Gammeltoft, Steen

AU - Hoffmann, Else Kay

PY - 2010/10/1

Y1 - 2010/10/1

N2 - The swelling-activated K(+) currents (I(K,vol)) in Ehrlich ascites tumor cells (EATC) has been reported to be through the two-pore domain (K(2p)), TWIK-related acid-sensitive K(+) channel 2 (TASK-2). The regulatory volume decrease (RVD), following hypotonic exposure in EATC, is rate limited by I(K,vol) indicating that inhibition of RVD reflects inhibition of TASK-2. We find that in EATC the tyrosine kinase inhibitor genistein inhibits RVD by 90%, and that the tyrosine phosphatase inhibitor monoperoxo(picolinato)-oxo-vanadate(V) [mpV(pic)] shifted the volume set point for inactivation of the channel to a lower cell volume. Swelling-activated K(+) efflux was impaired by genistein and the Src kinase family inhibitor 4-amino-5-(4-chloro-phenyl)-7-(t-butyl)pyrazolo[3,4-d]pyrimidine (PP2) and enhanced by the tyrosine phosphatase inhibitor mpV(pic). With the use of the TASK-2 inhibitor clofilium, it is demonstrated that mpV(pic) increased the volume-sensitive part of the K(+) efflux 1.3 times. To exclude K(+) efflux via a KCl cotransporter, cellular Cl(-) was substituted with NO(3)(-). Also under these conditions K(+) efflux was completely blocked by genistein. Thus tyrosine kinases seem to be involved in the activation of the volume-sensitive K(+) channel, whereas tyrosine phosphatases appears to be involved in inactivation of the channel. Overexpressing TASK-2 in human embryonic kidney (HEK)-293 cells increased the RVD rate and reduced the volume set point. TASK-2 has tyrosine sites, and precipitation of TASK-2 together with Western blotting and antibodies against phosphotyrosines revealed a cell swelling-induced, time-dependent tyrosine phosphorylation of the channel. Even though we found an inhibiting effect of PP2 on RVD, neither Src nor the focal adhesion kinase (FAK) seem to be involved. Inhibitors of the epidermal growth factor receptor tyrosine kinases had no effect on RVD, whereas the Janus kinase (JAK) inhibitor cucurbitacin inhibited the RVD by 40%. It is suggested that the cytokine receptor-coupled JAK/STAT pathway is upstream of the swelling-induced phosphorylation and activation of TASK-2 in EATC.

AB - The swelling-activated K(+) currents (I(K,vol)) in Ehrlich ascites tumor cells (EATC) has been reported to be through the two-pore domain (K(2p)), TWIK-related acid-sensitive K(+) channel 2 (TASK-2). The regulatory volume decrease (RVD), following hypotonic exposure in EATC, is rate limited by I(K,vol) indicating that inhibition of RVD reflects inhibition of TASK-2. We find that in EATC the tyrosine kinase inhibitor genistein inhibits RVD by 90%, and that the tyrosine phosphatase inhibitor monoperoxo(picolinato)-oxo-vanadate(V) [mpV(pic)] shifted the volume set point for inactivation of the channel to a lower cell volume. Swelling-activated K(+) efflux was impaired by genistein and the Src kinase family inhibitor 4-amino-5-(4-chloro-phenyl)-7-(t-butyl)pyrazolo[3,4-d]pyrimidine (PP2) and enhanced by the tyrosine phosphatase inhibitor mpV(pic). With the use of the TASK-2 inhibitor clofilium, it is demonstrated that mpV(pic) increased the volume-sensitive part of the K(+) efflux 1.3 times. To exclude K(+) efflux via a KCl cotransporter, cellular Cl(-) was substituted with NO(3)(-). Also under these conditions K(+) efflux was completely blocked by genistein. Thus tyrosine kinases seem to be involved in the activation of the volume-sensitive K(+) channel, whereas tyrosine phosphatases appears to be involved in inactivation of the channel. Overexpressing TASK-2 in human embryonic kidney (HEK)-293 cells increased the RVD rate and reduced the volume set point. TASK-2 has tyrosine sites, and precipitation of TASK-2 together with Western blotting and antibodies against phosphotyrosines revealed a cell swelling-induced, time-dependent tyrosine phosphorylation of the channel. Even though we found an inhibiting effect of PP2 on RVD, neither Src nor the focal adhesion kinase (FAK) seem to be involved. Inhibitors of the epidermal growth factor receptor tyrosine kinases had no effect on RVD, whereas the Janus kinase (JAK) inhibitor cucurbitacin inhibited the RVD by 40%. It is suggested that the cytokine receptor-coupled JAK/STAT pathway is upstream of the swelling-induced phosphorylation and activation of TASK-2 in EATC.

KW - Animals

KW - Cell Line

KW - Cell Size

KW - Enzyme Inhibitors

KW - Female

KW - Genistein

KW - Humans

KW - Hypotonic Solutions

KW - Janus Kinases

KW - Mice

KW - Patch-Clamp Techniques

KW - Phosphorylation

KW - Potassium

KW - Potassium Channels, Tandem Pore Domain

KW - Protein-Tyrosine Kinases

KW - STAT Transcription Factors

KW - Signal Transduction

KW - Tyrosine

U2 - 10.1152/ajpcell.00024.2010

DO - 10.1152/ajpcell.00024.2010

M3 - Journal article

C2 - 20631251

VL - 299

SP - C844-53

JO - American Journal of Physiology - Cell Physiology

JF - American Journal of Physiology - Cell Physiology

SN - 0363-6143

IS - 4

ER -

ID: 33884807