KCNK5 is functionally down-regulated upon long-term hypotonicity in Ehrlich ascites tumor cells

Research output: Contribution to journalJournal articleResearchpeer-review

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KCNK5 is functionally down-regulated upon long-term hypotonicity in Ehrlich ascites tumor cells. / Kirkegaard, Signe Skyum; Wulff, Tune; Gammeltoft, Steen; Hoffmann, Else Kay.

In: Cellular Physiology and Biochemistry, Vol. 32, No. 5, 2013, p. 1238-1246.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Kirkegaard, SS, Wulff, T, Gammeltoft, S & Hoffmann, EK 2013, 'KCNK5 is functionally down-regulated upon long-term hypotonicity in Ehrlich ascites tumor cells', Cellular Physiology and Biochemistry, vol. 32, no. 5, pp. 1238-1246. https://doi.org/10.1159/000354522

APA

Kirkegaard, S. S., Wulff, T., Gammeltoft, S., & Hoffmann, E. K. (2013). KCNK5 is functionally down-regulated upon long-term hypotonicity in Ehrlich ascites tumor cells. Cellular Physiology and Biochemistry, 32(5), 1238-1246. https://doi.org/10.1159/000354522

Vancouver

Kirkegaard SS, Wulff T, Gammeltoft S, Hoffmann EK. KCNK5 is functionally down-regulated upon long-term hypotonicity in Ehrlich ascites tumor cells. Cellular Physiology and Biochemistry. 2013;32(5):1238-1246. https://doi.org/10.1159/000354522

Author

Kirkegaard, Signe Skyum ; Wulff, Tune ; Gammeltoft, Steen ; Hoffmann, Else Kay. / KCNK5 is functionally down-regulated upon long-term hypotonicity in Ehrlich ascites tumor cells. In: Cellular Physiology and Biochemistry. 2013 ; Vol. 32, No. 5. pp. 1238-1246.

Bibtex

@article{df589de2b7b74932bf01ced961f7f211,
title = "KCNK5 is functionally down-regulated upon long-term hypotonicity in Ehrlich ascites tumor cells",
abstract = "Background/Aims: Regulatory volume decrease (RVD) in response to acute cell swelling is well described and KCNK5 (also known as TASK-2 or K2P5.1) has been shown to be the volume sensitive K(+) channel in Ehrlich cells. Very little is, on the other hand, known about the effects of long-term hypotonicity on expression and function of KCNK5, thus we have investigated the effect of long-term hypotonicity (24h - 48h) on KCNK5 in Ehrlich cells on the mRNA, protein and physiological levels. Methods: Physiological effects of long-term hypotonicity were measured using patch-clamp and Coulter counter techniques. Expression patterns of KCNK5 on mRNA and protein levels were established using real-time qPCR and western blotting respectively. Results: The maximum swelling-activated current through KCNK5 was significantly decreased upon 48h of hypotonicity and likewise the RVD response was significantly impaired after both 24 and 48h of hypotonic stimulation. No significant differences in the KCNK5 mRNA expression patterns between control and stimulated cells were observed, but a significant decrease in the KCNK5 protein level 48h after stimulation was found. Conclusion: The data suggest that the strong physiological impairment of KCNK5 in Ehrlich cells after long-term hypotonic stimulation is predominantly due to down-regulation of the KCNK5 protein synthesis. {\textcopyright} 2013 S. Karger AG, Basel.",
author = "Kirkegaard, {Signe Skyum} and Tune Wulff and Steen Gammeltoft and Hoffmann, {Else Kay}",
year = "2013",
doi = "10.1159/000354522",
language = "English",
volume = "32",
pages = "1238--1246",
journal = "Cellular Physiology and Biochemistry",
issn = "1015-8987",
publisher = "S Karger AG",
number = "5",

}

RIS

TY - JOUR

T1 - KCNK5 is functionally down-regulated upon long-term hypotonicity in Ehrlich ascites tumor cells

AU - Kirkegaard, Signe Skyum

AU - Wulff, Tune

AU - Gammeltoft, Steen

AU - Hoffmann, Else Kay

PY - 2013

Y1 - 2013

N2 - Background/Aims: Regulatory volume decrease (RVD) in response to acute cell swelling is well described and KCNK5 (also known as TASK-2 or K2P5.1) has been shown to be the volume sensitive K(+) channel in Ehrlich cells. Very little is, on the other hand, known about the effects of long-term hypotonicity on expression and function of KCNK5, thus we have investigated the effect of long-term hypotonicity (24h - 48h) on KCNK5 in Ehrlich cells on the mRNA, protein and physiological levels. Methods: Physiological effects of long-term hypotonicity were measured using patch-clamp and Coulter counter techniques. Expression patterns of KCNK5 on mRNA and protein levels were established using real-time qPCR and western blotting respectively. Results: The maximum swelling-activated current through KCNK5 was significantly decreased upon 48h of hypotonicity and likewise the RVD response was significantly impaired after both 24 and 48h of hypotonic stimulation. No significant differences in the KCNK5 mRNA expression patterns between control and stimulated cells were observed, but a significant decrease in the KCNK5 protein level 48h after stimulation was found. Conclusion: The data suggest that the strong physiological impairment of KCNK5 in Ehrlich cells after long-term hypotonic stimulation is predominantly due to down-regulation of the KCNK5 protein synthesis. © 2013 S. Karger AG, Basel.

AB - Background/Aims: Regulatory volume decrease (RVD) in response to acute cell swelling is well described and KCNK5 (also known as TASK-2 or K2P5.1) has been shown to be the volume sensitive K(+) channel in Ehrlich cells. Very little is, on the other hand, known about the effects of long-term hypotonicity on expression and function of KCNK5, thus we have investigated the effect of long-term hypotonicity (24h - 48h) on KCNK5 in Ehrlich cells on the mRNA, protein and physiological levels. Methods: Physiological effects of long-term hypotonicity were measured using patch-clamp and Coulter counter techniques. Expression patterns of KCNK5 on mRNA and protein levels were established using real-time qPCR and western blotting respectively. Results: The maximum swelling-activated current through KCNK5 was significantly decreased upon 48h of hypotonicity and likewise the RVD response was significantly impaired after both 24 and 48h of hypotonic stimulation. No significant differences in the KCNK5 mRNA expression patterns between control and stimulated cells were observed, but a significant decrease in the KCNK5 protein level 48h after stimulation was found. Conclusion: The data suggest that the strong physiological impairment of KCNK5 in Ehrlich cells after long-term hypotonic stimulation is predominantly due to down-regulation of the KCNK5 protein synthesis. © 2013 S. Karger AG, Basel.

U2 - 10.1159/000354522

DO - 10.1159/000354522

M3 - Journal article

C2 - 24247225

VL - 32

SP - 1238

EP - 1246

JO - Cellular Physiology and Biochemistry

JF - Cellular Physiology and Biochemistry

SN - 1015-8987

IS - 5

ER -

ID: 94832599