Modeling of the adrenergic response of the human I^sub Ks^ current (hKCNQ1/hKCNE1) stably expressed in HEK-293 cells
Stable coexpression of human (h)KCNQ1 and hKCNE1 in human embryonic kidney (HEK)-293 cells reconstitutes a nativelike slowly activating delayed rectifier ... current (HEK-I...), allowing β-adrenergic modulation of the current by stimulation of endogenous receptors in the host cell line. HEK-I... was...
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Veröffentlicht in: | American journal of physiology. Heart and circulatory physiology 2008-11, Vol.295 (5), p.H1867 |
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creator | Imredy, John P Penniman, Jacob R Dech, Spencer J Irving, Winston D Salata, Joseph J |
description | Stable coexpression of human (h)KCNQ1 and hKCNE1 in human embryonic kidney (HEK)-293 cells reconstitutes a nativelike slowly activating delayed rectifier ... current (HEK-I...), allowing β-adrenergic modulation of the current by stimulation of endogenous receptors in the host cell line. HEK-I... was enhanced two- to fourfold by isoproterenol (EC... = 13 nM), forskolin (10 ...M), or 8-(4-chlorophenylthio)adenosine 3',5'-cyclic monophosphate (50 ...M), indicating an intact cAMP-dependent ion channel-regulating pathway analogous to the PKA-dependent regulation observed in native cardiac myocytes. Activation kinetics of HEK-IKs were accurately fit with a novel modified second-order Hodgkin-Huxley (H-H) gating model incorporating a fast and a slow gate, each independent of each other in scale and adrenergic response, or a "heterodimer" model. Macroscopically, β-adrenergic enhancement shifted the current activation threshold to more negative potentials and accelerated activation kinetics while leaving deactivation kinetics relatively unaffected. Modeling of the current response using the H-H model indicated that observed changes in gating could be explained by modulation of the opening rate of the fast gate. Under control conditions at nearly physiological temperatures (35...C), rate-dependent accumulation of HEK-I... was observed only at pulse frequencies exceeding 3 Hz. Rate-dependent accumulation of I... at high pulsing rate had two phases, an initial staircaselike effect followed by a slower, incremental accumulation phase. These phases are readily interpreted in the context of a heterodimeric H-H model with two independent gates with differing closing rates. In the presence of isoproterenol after normalizing for its tonic effects, rate-dependent accumulation of HEK-I... appeared at lower pulse frequencies and was slightly enhanced (...25%) over control. (ProQuest: ... denotes formulae/symbols omitted.) |
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HEK-I... was enhanced two- to fourfold by isoproterenol (EC... = 13 nM), forskolin (10 ...M), or 8-(4-chlorophenylthio)adenosine 3',5'-cyclic monophosphate (50 ...M), indicating an intact cAMP-dependent ion channel-regulating pathway analogous to the PKA-dependent regulation observed in native cardiac myocytes. Activation kinetics of HEK-IKs were accurately fit with a novel modified second-order Hodgkin-Huxley (H-H) gating model incorporating a fast and a slow gate, each independent of each other in scale and adrenergic response, or a "heterodimer" model. Macroscopically, β-adrenergic enhancement shifted the current activation threshold to more negative potentials and accelerated activation kinetics while leaving deactivation kinetics relatively unaffected. Modeling of the current response using the H-H model indicated that observed changes in gating could be explained by modulation of the opening rate of the fast gate. Under control conditions at nearly physiological temperatures (35...C), rate-dependent accumulation of HEK-I... was observed only at pulse frequencies exceeding 3 Hz. Rate-dependent accumulation of I... at high pulsing rate had two phases, an initial staircaselike effect followed by a slower, incremental accumulation phase. These phases are readily interpreted in the context of a heterodimeric H-H model with two independent gates with differing closing rates. In the presence of isoproterenol after normalizing for its tonic effects, rate-dependent accumulation of HEK-I... appeared at lower pulse frequencies and was slightly enhanced (...25%) over control. 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Heart and circulatory physiology</title><description>Stable coexpression of human (h)KCNQ1 and hKCNE1 in human embryonic kidney (HEK)-293 cells reconstitutes a nativelike slowly activating delayed rectifier ... current (HEK-I...), allowing β-adrenergic modulation of the current by stimulation of endogenous receptors in the host cell line. HEK-I... was enhanced two- to fourfold by isoproterenol (EC... = 13 nM), forskolin (10 ...M), or 8-(4-chlorophenylthio)adenosine 3',5'-cyclic monophosphate (50 ...M), indicating an intact cAMP-dependent ion channel-regulating pathway analogous to the PKA-dependent regulation observed in native cardiac myocytes. Activation kinetics of HEK-IKs were accurately fit with a novel modified second-order Hodgkin-Huxley (H-H) gating model incorporating a fast and a slow gate, each independent of each other in scale and adrenergic response, or a "heterodimer" model. Macroscopically, β-adrenergic enhancement shifted the current activation threshold to more negative potentials and accelerated activation kinetics while leaving deactivation kinetics relatively unaffected. Modeling of the current response using the H-H model indicated that observed changes in gating could be explained by modulation of the opening rate of the fast gate. Under control conditions at nearly physiological temperatures (35...C), rate-dependent accumulation of HEK-I... was observed only at pulse frequencies exceeding 3 Hz. Rate-dependent accumulation of I... at high pulsing rate had two phases, an initial staircaselike effect followed by a slower, incremental accumulation phase. These phases are readily interpreted in the context of a heterodimeric H-H model with two independent gates with differing closing rates. In the presence of isoproterenol after normalizing for its tonic effects, rate-dependent accumulation of HEK-I... appeared at lower pulse frequencies and was slightly enhanced (...25%) over control. 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Heart and circulatory physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Imredy, John P</au><au>Penniman, Jacob R</au><au>Dech, Spencer J</au><au>Irving, Winston D</au><au>Salata, Joseph J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Modeling of the adrenergic response of the human I^sub Ks^ current (hKCNQ1/hKCNE1) stably expressed in HEK-293 cells</atitle><jtitle>American journal of physiology. Heart and circulatory physiology</jtitle><date>2008-11-01</date><risdate>2008</risdate><volume>295</volume><issue>5</issue><spage>H1867</spage><pages>H1867-</pages><issn>0363-6135</issn><eissn>1522-1539</eissn><coden>AJPPDI</coden><abstract>Stable coexpression of human (h)KCNQ1 and hKCNE1 in human embryonic kidney (HEK)-293 cells reconstitutes a nativelike slowly activating delayed rectifier ... current (HEK-I...), allowing β-adrenergic modulation of the current by stimulation of endogenous receptors in the host cell line. HEK-I... was enhanced two- to fourfold by isoproterenol (EC... = 13 nM), forskolin (10 ...M), or 8-(4-chlorophenylthio)adenosine 3',5'-cyclic monophosphate (50 ...M), indicating an intact cAMP-dependent ion channel-regulating pathway analogous to the PKA-dependent regulation observed in native cardiac myocytes. Activation kinetics of HEK-IKs were accurately fit with a novel modified second-order Hodgkin-Huxley (H-H) gating model incorporating a fast and a slow gate, each independent of each other in scale and adrenergic response, or a "heterodimer" model. Macroscopically, β-adrenergic enhancement shifted the current activation threshold to more negative potentials and accelerated activation kinetics while leaving deactivation kinetics relatively unaffected. Modeling of the current response using the H-H model indicated that observed changes in gating could be explained by modulation of the opening rate of the fast gate. Under control conditions at nearly physiological temperatures (35...C), rate-dependent accumulation of HEK-I... was observed only at pulse frequencies exceeding 3 Hz. Rate-dependent accumulation of I... at high pulsing rate had two phases, an initial staircaselike effect followed by a slower, incremental accumulation phase. These phases are readily interpreted in the context of a heterodimeric H-H model with two independent gates with differing closing rates. In the presence of isoproterenol after normalizing for its tonic effects, rate-dependent accumulation of HEK-I... appeared at lower pulse frequencies and was slightly enhanced (...25%) over control. (ProQuest: ... denotes formulae/symbols omitted.)</abstract><cop>Bethesda</cop><pub>American Physiological Society</pub></addata></record> |
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source | American Physiological Society; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | Cardiovascular system Cells Embryology Embryos Heart Kidneys Pharmacology Potassium |
title | Modeling of the adrenergic response of the human I^sub Ks^ current (hKCNQ1/hKCNE1) stably expressed in HEK-293 cells |
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