Source:http://linkedlifedata.com/resource/pubmed/id/20568224
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2010-9-15
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pubmed:abstractText |
HL-1 is a line of immortalized cells of cardiomyocyte origin that are a useful complement to native cardiomyocytes in studies of cardiac gene regulation. Several types of ion channel have been identified in these cells, but not the physiologically important inward rectifier K(+) channels. Our aim was to identify and characterize inward rectifier K(+) channels in HL-1 cells. External Ba(2+) (100?µM) inhibited 44?±?0.05% (mean?±?s.e.m., n?=?11) of inward current in whole-cell patch-clamp recordings. The reversal potential of the Ba(2+)-sensitive current shifted with external [K(+)] as expected for K(+)-selective channels. The slope conductance of the inward Ba(2+)-sensitive current increased with external [K(+)]. The apparent Kd for Ba(2+) was voltage dependent, ranging from 15?µM at -150 ?mV to 148?µM at -75 ?mV in 120 ?mM external K(+). This current was insensitive to 10?µM glybenclamide. A component of whole-cell current was sensitive to 150?µM 4,4'-diisothiocyanatostilbene-2,2'-disulfonic acid (DIDS), although it did not correspond to the Ba(2+)-sensitive component. The effect of external 1 mM Cs(+) was similar to that of Ba(2+). Polymerase chain reaction using HL-1 cDNA as template and primers specific for the cardiac inward rectifier K(ir)2.1 produced a fragment of the expected size that was confirmed to be K(ir)2.1 by DNA sequencing. In conclusion, HL-1 cells express a current that is characteristic of cardiac inward rectifier K(+) channels, and express K(ir)2.1 mRNA. This cell line may have use as a system for studying inward rectifier gene regulation in a cardiomyocyte phenotype.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Barium,
http://linkedlifedata.com/resource/pubmed/chemical/Cesium,
http://linkedlifedata.com/resource/pubmed/chemical/Kir2.1 channel,
http://linkedlifedata.com/resource/pubmed/chemical/Potassium,
http://linkedlifedata.com/resource/pubmed/chemical/Potassium Channel Blockers,
http://linkedlifedata.com/resource/pubmed/chemical/Potassium Channels, Inwardly...,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
1097-4652
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pubmed:author | |
pubmed:copyrightInfo |
© 2010 Wiley-Liss, Inc.
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pubmed:issnType |
Electronic
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pubmed:volume |
225
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
751-6
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pubmed:meshHeading |
pubmed-meshheading:20568224-Animals,
pubmed-meshheading:20568224-Barium,
pubmed-meshheading:20568224-Cell Line,
pubmed-meshheading:20568224-Cesium,
pubmed-meshheading:20568224-Membrane Potentials,
pubmed-meshheading:20568224-Mice,
pubmed-meshheading:20568224-Myocytes, Cardiac,
pubmed-meshheading:20568224-Patch-Clamp Techniques,
pubmed-meshheading:20568224-Phenotype,
pubmed-meshheading:20568224-Potassium,
pubmed-meshheading:20568224-Potassium Channel Blockers,
pubmed-meshheading:20568224-Potassium Channels, Inwardly Rectifying,
pubmed-meshheading:20568224-RNA, Messenger,
pubmed-meshheading:20568224-Reverse Transcriptase Polymerase Chain Reaction,
pubmed-meshheading:20568224-Time Factors
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pubmed:year |
2010
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pubmed:articleTitle |
Inward rectifier potassium channels in the HL-1 cardiomyocyte-derived cell line.
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pubmed:affiliation |
Cardiovascular Remodelling Group, Centre for Vision and Vascular Science, School of Medicine, Dentistry and Biomedical Sciences, Queen's University, Belfast, UK.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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