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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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Detalles Bibliográficos
Autores principales: Zhang, Hengtao, Parker, Jeremy, Shepherd, Neal, Creazzo, Tony L
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
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
Descripción
Sumario: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).