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TASK-2: a K(2P) K(+) channel with complex regulation and diverse physiological functions

TASK-2 (K(2P)5.1) is a two-pore domain K(+) channel belonging to the TALK subgroup of the K(2P) family of proteins. TASK-2 has been shown to be activated by extra- and intracellular alkalinization. Extra- and intracellular pH-sensors reside at arginine 224 and lysine 245 and might affect separate se...

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Autores principales: Cid, L. Pablo, Roa-Rojas, Hugo A., Niemeyer, María I., González, Wendy, Araki, Masatake, Araki, Kimi, Sepúlveda, Francisco V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3725403/
https://www.ncbi.nlm.nih.gov/pubmed/23908634
http://dx.doi.org/10.3389/fphys.2013.00198
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author Cid, L. Pablo
Roa-Rojas, Hugo A.
Niemeyer, María I.
González, Wendy
Araki, Masatake
Araki, Kimi
Sepúlveda, Francisco V.
author_facet Cid, L. Pablo
Roa-Rojas, Hugo A.
Niemeyer, María I.
González, Wendy
Araki, Masatake
Araki, Kimi
Sepúlveda, Francisco V.
author_sort Cid, L. Pablo
collection PubMed
description TASK-2 (K(2P)5.1) is a two-pore domain K(+) channel belonging to the TALK subgroup of the K(2P) family of proteins. TASK-2 has been shown to be activated by extra- and intracellular alkalinization. Extra- and intracellular pH-sensors reside at arginine 224 and lysine 245 and might affect separate selectivity filter and inner gates respectively. TASK-2 is modulated by changes in cell volume and a regulation by direct G-protein interaction has also been proposed. Activation by extracellular alkalinization has been associated with a role of TASK-2 in kidney proximal tubule bicarbonate reabsorption, whilst intracellular pH-sensitivity might be the mechanism for its participation in central chemosensitive neurons. In addition to these functions TASK-2 has been proposed to play a part in apoptotic volume decrease in kidney cells and in volume regulation of glial cells and T-lymphocytes. TASK-2 is present in chondrocytes of hyaline cartilage, where it is proposed to play a central role in stabilizing the membrane potential. Additional sites of expression are dorsal root ganglion neurons, endocrine and exocrine pancreas and intestinal smooth muscle cells. TASK-2 has been associated with the regulation of proliferation of breast cancer cells and could become target for breast cancer therapeutics. Further work in native tissues and cells together with genetic modification will no doubt reveal the details of TASK-2 functions that we are only starting to suspect.
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spelling pubmed-37254032013-08-01 TASK-2: a K(2P) K(+) channel with complex regulation and diverse physiological functions Cid, L. Pablo Roa-Rojas, Hugo A. Niemeyer, María I. González, Wendy Araki, Masatake Araki, Kimi Sepúlveda, Francisco V. Front Physiol Physiology TASK-2 (K(2P)5.1) is a two-pore domain K(+) channel belonging to the TALK subgroup of the K(2P) family of proteins. TASK-2 has been shown to be activated by extra- and intracellular alkalinization. Extra- and intracellular pH-sensors reside at arginine 224 and lysine 245 and might affect separate selectivity filter and inner gates respectively. TASK-2 is modulated by changes in cell volume and a regulation by direct G-protein interaction has also been proposed. Activation by extracellular alkalinization has been associated with a role of TASK-2 in kidney proximal tubule bicarbonate reabsorption, whilst intracellular pH-sensitivity might be the mechanism for its participation in central chemosensitive neurons. In addition to these functions TASK-2 has been proposed to play a part in apoptotic volume decrease in kidney cells and in volume regulation of glial cells and T-lymphocytes. TASK-2 is present in chondrocytes of hyaline cartilage, where it is proposed to play a central role in stabilizing the membrane potential. Additional sites of expression are dorsal root ganglion neurons, endocrine and exocrine pancreas and intestinal smooth muscle cells. TASK-2 has been associated with the regulation of proliferation of breast cancer cells and could become target for breast cancer therapeutics. Further work in native tissues and cells together with genetic modification will no doubt reveal the details of TASK-2 functions that we are only starting to suspect. Frontiers Media S.A. 2013-07-29 /pmc/articles/PMC3725403/ /pubmed/23908634 http://dx.doi.org/10.3389/fphys.2013.00198 Text en Copyright © 2013 Cid, Roa-Rojas, Niemeyer, González, Araki, Araki and Sepúlveda. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Physiology
Cid, L. Pablo
Roa-Rojas, Hugo A.
Niemeyer, María I.
González, Wendy
Araki, Masatake
Araki, Kimi
Sepúlveda, Francisco V.
TASK-2: a K(2P) K(+) channel with complex regulation and diverse physiological functions
title TASK-2: a K(2P) K(+) channel with complex regulation and diverse physiological functions
title_full TASK-2: a K(2P) K(+) channel with complex regulation and diverse physiological functions
title_fullStr TASK-2: a K(2P) K(+) channel with complex regulation and diverse physiological functions
title_full_unstemmed TASK-2: a K(2P) K(+) channel with complex regulation and diverse physiological functions
title_short TASK-2: a K(2P) K(+) channel with complex regulation and diverse physiological functions
title_sort task-2: a k(2p) k(+) channel with complex regulation and diverse physiological functions
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3725403/
https://www.ncbi.nlm.nih.gov/pubmed/23908634
http://dx.doi.org/10.3389/fphys.2013.00198
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