<HashMap><database>biostudies-other</database><scores/><additional><submitter>Du DT</submitter><funding>British Heart Foundation</funding><funding>Medical Research Council</funding><pagination>1-4</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4286594</full_dataset_link><abstract>Previous studies investigating human induced pluripotent stem cell-derived cardiomyocytes (iPSC-CMs) have proposed the distinction of heart chamber-specific (atrial, ventricular, pacemaker) electrophysiological phenotypes based on action potential (AP) morphology. This suggestion has been based on data acquired using techniques that allow measurements from only a small number of cells and at low seeding densities. It has also been observed that density of culture affects the properties of iPSC-CMs. Here we systematically analyze AP morphology from iPSC-CMs at two seeding densities: 60,000 cells/well (confluent monolayer) and 15,000 cells/well (sparsely-seeded) using a noninvasive optical method. The confluent cells (n = 360) demonstrate a series of AP morphologies on a normally distributed spectrum with no evidence for specific subpopulations. The AP morphologies of sparsely seeded cells (n = 32) displayed a significantly different distribution, but even in this case there is no clear evidence of chamber-specificity. Reduction in gap junction conductance using carbenoxolone only minimally affected APD distribution in confluent cells. These data suggest that iPSC-CMs possess a sui generis AP morphology, and when observed in different seeding densities may encompass any shape including those resembling chamber-specific subtypes. These results may be explained by different functional maturation due to culture conditions.</abstract><repository>biostudies-other</repository><data_source>Europe PMC</data_source><omics_type>Unknown</omics_type><volume>108(1)</volume><journal>Biophysical journal</journal><pmcid>PMC4286594</pmcid><funding_grant_id>FS/13/46/30282</funding_grant_id><funding_grant_id>MR/L012618/1</funding_grant_id><pubmed_authors>Hellen N</pubmed_authors><pubmed_authors>Kane C</pubmed_authors><pubmed_authors>Du DT</pubmed_authors><pubmed_authors>Terracciano CM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Action potential morphology of human induced pluripotent stem cell-derived cardiomyocytes does not predict cardiac chamber specificity and is dependent on cell density.</name><description>Previous studies investigating human induced pluripotent stem cell-derived cardiomyocytes (iPSC-CMs) have proposed the distinction of heart chamber-specific (atrial, ventricular, pacemaker) electrophysiological phenotypes based on action potential (AP) morphology. This suggestion has been based on data acquired using techniques that allow measurements from only a small number of cells and at low seeding densities. It has also been observed that density of culture affects the properties of iPSC-CMs. Here we systematically analyze AP morphology from iPSC-CMs at two seeding densities: 60,000 cells/well (confluent monolayer) and 15,000 cells/well (sparsely-seeded) using a noninvasive optical method. The confluent cells (n = 360) demonstrate a series of AP morphologies on a normally distributed spectrum with no evidence for specific subpopulations. The AP morphologies of sparsely seeded cells (n = 32) displayed a significantly different distribution, but even in this case there is no clear evidence of chamber-specificity. Reduction in gap junction conductance using carbenoxolone only minimally affected APD distribution in confluent cells. These data suggest that iPSC-CMs possess a sui generis AP morphology, and when observed in different seeding densities may encompass any shape including those resembling chamber-specific subtypes. These results may be explained by different functional maturation due to culture conditions.</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Jan</publication><modification>2019-03-27T01:42:54Z</modification><creation>2019-03-27T01:42:54Z</creation></dates><accession>S-EPMC4286594</accession><cross_references><pubmed>25564842</pubmed><doi>10.1016/j.bpj.2014.11.008 </doi></cross_references></HashMap>