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Article: Physical developmental cues for the maturation of human pluripotent stem cell-derived cardiomyocytes

TitlePhysical developmental cues for the maturation of human pluripotent stem cell-derived cardiomyocytes
Authors
Issue Date2014
PublisherBioMed Central Ltd.
Citation
Stem cell research & therapy, 2014, v. 5, n. 1, p. 117 How to Cite?
AbstractHuman pluripotent stem cell-derived cardiomyocytes (hPSC-CMs) are the most promising source of cardiomyocytes (CMs) for experimental and clinical applications, but their use is largely limited by a structurally and functionally immature phenotype that most closely resembles embryonic or fetal heart cells. The application of physical stimuli to influence hPSC-CMs through mechanical and bioelectrical transduction offers a powerful strategy for promoting more developmentally mature CMs. Here we summarize the major events associated with in vivo heart maturation and structural development. We then review the developmental state of in vitro derived hPSC-CMs, while focusing on physical (electrical and mechanical) stimuli and contributory (metabolic and hypertrophic) factors that are actively involved in structural and functional adaptations of hPSC-CMs. Finally, we highlight areas for possible future investigation that should provide a better understanding of how physical stimuli may promote in vitro development and lead to mechanistic insights. Advances in the use of physical stimuli to promote developmental maturation will be required to overcome current limitations and significantly advance research of hPSC-CMs for cardiac disease modeling, in vitro drug screening, cardiotoxicity analysis and therapeutic applications.
Persistent Identifierhttp://hdl.handle.net/10722/237130
ISSN
2023 Impact Factor: 7.1
2023 SCImago Journal Rankings: 1.798
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorZhu, Renjun-
dc.contributor.authorBlazeski, Adriana-
dc.contributor.authorPoon, Ellen-
dc.contributor.authorCosta, Kevin D.-
dc.contributor.authorTung, Leslie-
dc.contributor.authorBoheler, Kenneth R.-
dc.date.accessioned2016-12-20T06:48:42Z-
dc.date.available2016-12-20T06:48:42Z-
dc.date.issued2014-
dc.identifier.citationStem cell research & therapy, 2014, v. 5, n. 1, p. 117-
dc.identifier.issn1757-6512-
dc.identifier.urihttp://hdl.handle.net/10722/237130-
dc.description.abstractHuman pluripotent stem cell-derived cardiomyocytes (hPSC-CMs) are the most promising source of cardiomyocytes (CMs) for experimental and clinical applications, but their use is largely limited by a structurally and functionally immature phenotype that most closely resembles embryonic or fetal heart cells. The application of physical stimuli to influence hPSC-CMs through mechanical and bioelectrical transduction offers a powerful strategy for promoting more developmentally mature CMs. Here we summarize the major events associated with in vivo heart maturation and structural development. We then review the developmental state of in vitro derived hPSC-CMs, while focusing on physical (electrical and mechanical) stimuli and contributory (metabolic and hypertrophic) factors that are actively involved in structural and functional adaptations of hPSC-CMs. Finally, we highlight areas for possible future investigation that should provide a better understanding of how physical stimuli may promote in vitro development and lead to mechanistic insights. Advances in the use of physical stimuli to promote developmental maturation will be required to overcome current limitations and significantly advance research of hPSC-CMs for cardiac disease modeling, in vitro drug screening, cardiotoxicity analysis and therapeutic applications.-
dc.languageeng-
dc.publisherBioMed Central Ltd.-
dc.relation.ispartofStem cell research & therapy-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.titlePhysical developmental cues for the maturation of human pluripotent stem cell-derived cardiomyocytes-
dc.typeArticle-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1186/scrt507-
dc.identifier.pmid25688759-
dc.identifier.scopuseid_2-s2.0-84988599499-
dc.identifier.hkuros251603-
dc.identifier.volume5-
dc.identifier.issue5-
dc.identifier.spage117-
dc.identifier.eissn1757-6512-
dc.identifier.isiWOS:000344573600001-
dc.identifier.issnl1757-6512-

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