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Developmental expression of a functional TASK-1 2P domain K(+ )channel in embryonic chick heart
BACKGROUND: Background K(+ )channels are the principal determinants of the resting membrane potential (RMP) in cardiac myocytes and thus, influence the magnitude and time course of the action potential (AP). METHODS: RT-PCR and in situ hybridization are used to study the distribution of TASK-1 and w...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2788539/ https://www.ncbi.nlm.nih.gov/pubmed/19930646 http://dx.doi.org/10.1186/1423-0127-16-104 |
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author | Zhang, Hengtao Parker, Jeremy Shepherd, Neal Creazzo, Tony L |
author_facet | Zhang, Hengtao Parker, Jeremy Shepherd, Neal Creazzo, Tony L |
author_sort | Zhang, Hengtao |
collection | PubMed |
description | BACKGROUND: Background K(+ )channels are the principal determinants of the resting membrane potential (RMP) in cardiac myocytes and thus, influence the magnitude and time course of the action potential (AP). METHODS: RT-PCR and in situ hybridization are used to study the distribution of TASK-1 and whole-cell patch clamp technique is employed to determine the functional expression of TASK-1 in embryonic chick heart. RESULTS: Chicken TASK-1 was expressed in the early tubular heart, then substantially decreased in the ventricles by embryonic day 5 (ED5), but remained relatively high in ED5 and ED11 atria. Unlike TASK-1, TASK-3 was uniformly expressed in heart at all developmental stages. In situ hybridization studies further revealed that TASK-1 was expressed throughout myocardium at Hamilton-Hamburger stages 11 and 18 (S11 & S18) heart. In ED11 heart, TASK-1 expression was more restricted to atria. Consistent with TASK-1 expression data, patch clamp studies indicated that there was little TASK-1 current, as measured by the difference currents between pH 8.4 and pH 7.4, in ED5 and ED11 ventricular myocytes. However, TASK-1 current was present in the early embryonic heart and ED11 atrial myocytes. TASK-1 currents were also identified as 3 μM anandamide-sensitive currents. 3 μM anandamide reduced TASK-1 currents by about 58% in ED11 atrial myocytes. Zn(2+ )(100 μM) which selectively inhibits TASK-3 channel at this concentration had no effect on TASK currents. In ED11 ventricle where TASK-1 expression was down-regulated, I(K1 )was about 5 times greater than in ED11 atrial myocytes. CONCLUSION: Functional TASK-1 channels are differentially expressed in the developing chick heart and TASK-1 channels contribute to background K(+ )conductance in the early tubular embryonic heart and in atria. TASK-1 channels act as a contributor to background K(+ )current to modulate the cardiac excitability in the embryonic heart that expresses little I(K1). |
format | Text |
id | pubmed-2788539 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-27885392009-12-04 Developmental expression of a functional TASK-1 2P domain K(+ )channel in embryonic chick heart Zhang, Hengtao Parker, Jeremy Shepherd, Neal Creazzo, Tony L J Biomed Sci Research BACKGROUND: Background K(+ )channels are the principal determinants of the resting membrane potential (RMP) in cardiac myocytes and thus, influence the magnitude and time course of the action potential (AP). METHODS: RT-PCR and in situ hybridization are used to study the distribution of TASK-1 and whole-cell patch clamp technique is employed to determine the functional expression of TASK-1 in embryonic chick heart. RESULTS: Chicken TASK-1 was expressed in the early tubular heart, then substantially decreased in the ventricles by embryonic day 5 (ED5), but remained relatively high in ED5 and ED11 atria. Unlike TASK-1, TASK-3 was uniformly expressed in heart at all developmental stages. In situ hybridization studies further revealed that TASK-1 was expressed throughout myocardium at Hamilton-Hamburger stages 11 and 18 (S11 & S18) heart. In ED11 heart, TASK-1 expression was more restricted to atria. Consistent with TASK-1 expression data, patch clamp studies indicated that there was little TASK-1 current, as measured by the difference currents between pH 8.4 and pH 7.4, in ED5 and ED11 ventricular myocytes. However, TASK-1 current was present in the early embryonic heart and ED11 atrial myocytes. TASK-1 currents were also identified as 3 μM anandamide-sensitive currents. 3 μM anandamide reduced TASK-1 currents by about 58% in ED11 atrial myocytes. Zn(2+ )(100 μM) which selectively inhibits TASK-3 channel at this concentration had no effect on TASK currents. In ED11 ventricle where TASK-1 expression was down-regulated, I(K1 )was about 5 times greater than in ED11 atrial myocytes. CONCLUSION: Functional TASK-1 channels are differentially expressed in the developing chick heart and TASK-1 channels contribute to background K(+ )conductance in the early tubular embryonic heart and in atria. TASK-1 channels act as a contributor to background K(+ )current to modulate the cardiac excitability in the embryonic heart that expresses little I(K1). BioMed Central 2009-11-23 /pmc/articles/PMC2788539/ /pubmed/19930646 http://dx.doi.org/10.1186/1423-0127-16-104 Text en Copyright ©2009 Zhang et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Zhang, Hengtao Parker, Jeremy Shepherd, Neal Creazzo, Tony L Developmental expression of a functional TASK-1 2P domain K(+ )channel in embryonic chick heart |
title | Developmental expression of a functional TASK-1 2P domain K(+ )channel in embryonic chick heart |
title_full | Developmental expression of a functional TASK-1 2P domain K(+ )channel in embryonic chick heart |
title_fullStr | Developmental expression of a functional TASK-1 2P domain K(+ )channel in embryonic chick heart |
title_full_unstemmed | Developmental expression of a functional TASK-1 2P domain K(+ )channel in embryonic chick heart |
title_short | Developmental expression of a functional TASK-1 2P domain K(+ )channel in embryonic chick heart |
title_sort | developmental expression of a functional task-1 2p domain k(+ )channel in embryonic chick heart |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2788539/ https://www.ncbi.nlm.nih.gov/pubmed/19930646 http://dx.doi.org/10.1186/1423-0127-16-104 |
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