Source:http://linkedlifedata.com/resource/pubmed/id/20303332
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2010-5-24
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pubmed:abstractText |
To improve proarrhythmic predictability of preclinical models, we assessed whether human ventricular-like embryonic stem cell-derived cardiomyocytes (hESC-CMs) can be selected following a standardized protocol. Also, we quantified their arrhythmogenic response and compared this to a contemporary used rabbit Purkinje fiber (PF) model. Multiple transmembrane action potentials (AP) were recorded from 164 hESC-CM clusters (9 different batches), and 12 isolated PFs from New Zealand White rabbits. AP duration (APD), early afterdepolarizations (EADs), triangulation (T), and short-term variability of repolarization (STV) were determined on application of the I(Kr) blocker E-4031 (0.03/0.1/0.3/1 muM). Isoproterenol (0.1 muM) was used to assess adrenergic response. To validate the phenotype, RNA isolated from atrial- and ventricular-like clusters (n=8) was analyzed using low-density Taqman arrays. Based on initial experiments, slow beating rate (<50 bpm) and long APD (>200 ms) were used to select 31 ventricular-like clusters. E-4031 (1 muM) prolonged APD (31/31) and induced EADs only in clusters with APD90>300 ms (11/16). EADs were associated with increased T (1.6+/-0.2 vs 2.0+/-0.3) and STV (2.7+/-1.5 vs 6.9+/-1.9). Rabbit PF reacted in a similar way with regards to EADs (5/12), increased T (1.3+/-0.1 vs 1.9+/-0.4), and STV (1.2+/-0.9 vs 7.1+/-5.6). According to ROC values, hESC-CMs (STV 0.91) could predict EADs at least equivalent to PF (STV 0.69). Isoproterenol shortened APD and completely suppressed EADs. Gene expression analysis revealed that HCN1/2, KCNA5, and GJA5 were higher in atrial/nodal-like cells, whereas KCNJ2 and SCN1B were higher in ventricular-like cells (P<0.05). Selection of hESC-CM clusters with a ventricular-like phenotype can be standardized. The proarrhythmic results are qualitatively and quantitatively comparable between hESC-CMs and rabbit PF. Our results indicate that additional validation of this new safety pharmacology model is warranted.
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pubmed:commentsCorrections | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Connexins,
http://linkedlifedata.com/resource/pubmed/chemical/Cyclic Nucleotide-Gated Cation...,
http://linkedlifedata.com/resource/pubmed/chemical/HCN2 potassium channel,
http://linkedlifedata.com/resource/pubmed/chemical/Ion Channels,
http://linkedlifedata.com/resource/pubmed/chemical/Isoproterenol,
http://linkedlifedata.com/resource/pubmed/chemical/Kir2.1 channel,
http://linkedlifedata.com/resource/pubmed/chemical/Kv1.5 Potassium Channel,
http://linkedlifedata.com/resource/pubmed/chemical/Potassium Channels,
http://linkedlifedata.com/resource/pubmed/chemical/Potassium Channels, Inwardly...,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/Sodium Channels,
http://linkedlifedata.com/resource/pubmed/chemical/connexin 40,
http://linkedlifedata.com/resource/pubmed/chemical/hyperpolarization-activated cation...
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
1876-7753
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pubmed:author | |
pubmed:copyrightInfo |
Copyright 2010 Elsevier B.V. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:volume |
4
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
189-200
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pubmed:meshHeading |
pubmed-meshheading:20303332-Action Potentials,
pubmed-meshheading:20303332-Animals,
pubmed-meshheading:20303332-Cell Line,
pubmed-meshheading:20303332-Connexins,
pubmed-meshheading:20303332-Cyclic Nucleotide-Gated Cation Channels,
pubmed-meshheading:20303332-Electrocardiography,
pubmed-meshheading:20303332-Embryonic Stem Cells,
pubmed-meshheading:20303332-Humans,
pubmed-meshheading:20303332-Ion Channels,
pubmed-meshheading:20303332-Isoproterenol,
pubmed-meshheading:20303332-Kv1.5 Potassium Channel,
pubmed-meshheading:20303332-Models, Biological,
pubmed-meshheading:20303332-Myocytes, Cardiac,
pubmed-meshheading:20303332-Phenotype,
pubmed-meshheading:20303332-Potassium Channels,
pubmed-meshheading:20303332-Potassium Channels, Inwardly Rectifying,
pubmed-meshheading:20303332-Purkinje Fibers,
pubmed-meshheading:20303332-RNA, Messenger,
pubmed-meshheading:20303332-Rabbits,
pubmed-meshheading:20303332-Sodium Channels
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pubmed:year |
2010
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pubmed:articleTitle |
Quantified proarrhythmic potential of selected human embryonic stem cell-derived cardiomyocytes.
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pubmed:affiliation |
Department of Medical Physiology, Division Heart & Lungs, University Medical Center Utrecht, Utrecht, The Netherlands. m.k.b.jonsson@umcutrecht.nl
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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