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TBAK-1 and TASK-1, two-pore K+ channel subunits: kinetic properties and expression in rat heart

Authors
Kim, YangmiBang, HyoweonKim, Donghee
Issue Date
Nov-1999
Publisher
AMER PHYSIOLOGICAL SOC
Keywords
two-pore potassium channel; atrial cell; pH
Citation
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, v.277, no.5, pp H1669 - H1678
Journal Title
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY
Volume
277
Number
5
Start Page
H1669
End Page
H1678
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/25382
DOI
10.1152/ajpheart.1999.277.5.h1669
ISSN
0363-6135
1522-1539
Abstract
TEAK-I and TASK-1, two-pore K+ channel subunits: kinetic properties and expression in rat heart. Am. J. Physiol. 277 (Heart Circ. Physiol. 46): H1669-H1678, 1999. -A mammalian K+ channel subunit (TBAK-1/TASK-1) containing two pore domains and four transmembrane segments and whose mRNA is highly expressed in the heart has been cloned recently. TEAK-I and TASK-1 are identical except for the additional nine amino acids in the NH2 terminus of TEAK-I. We examined their kinetic properties, pH sensitivity, and regional cardiac mRNA expression and determined whether a native cardiac K+ channel with similar kinetic properties was present. When TBAK-1 or TASK-1 was transiently expressed in COS-7 cells, time- and voltage-independent whole cell currents were observed. Single-channel conductances of TEAK-I and TASK-1 were 14.6 +/- 1.0 and 13.8 +/- 2.8 pS, respectively, at -80 mV in 140 mM extracellular K+, and the mean open times were 0.8 +/- 0.1 and 0.6 +/- 0.1 ms, respectively. Both TBAK-1 and TASK-1 were highly sensitive to extracellular pH such that a decrease from 7.2 to 6.4 reduced their open probability (P-o) by 81 +/- 14% and 80 +/- 16%, whereas a decrease in intracellular pH from 7.2 to 6.4 reduced the P-o by 42 +/- 10% and 47 +/- 12%, respectively. TBAK-1/TASK-1 mRNA was expressed in all regions of the rat heart, with the highest level of expression in the right atrium. A 14-pS K+ channel with kinetic properties similar to those of TBAK-1/TASK-1 was identified in rat atrial and ventricular cells. These results indicate that TBAK-1/TASK-1 represents a functional native K+ channel in the rat heart.
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