Generation of human iPSCs derived heart organoids structurally and functionally similar to heart

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dc.contributor.authorS G Lee-
dc.contributor.authorY J Kim-
dc.contributor.authorMi-Young Son-
dc.contributor.authorM S Oh-
dc.contributor.authorJ Kim-
dc.contributor.authorB Ryu-
dc.contributor.authorK R Kang-
dc.contributor.authorJ Baek-
dc.contributor.authorG Chung-
dc.contributor.authorD H Woo-
dc.contributor.authorS Y Kim-
dc.contributor.authorH M Chung-
dc.date.accessioned2022-10-25T16:32:39Z-
dc.date.available2022-10-25T16:32:39Z-
dc.date.issued2022-
dc.identifier.issn0142-9612-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/30503-
dc.description.abstractCurrently, due to the increasing demand for 3D culture, various organoids that mimic organs are being actively studied. Despite active reports, information on heart organoids (HOs), which are the first functional organs, is still insufficient. Parameters for reproducing hearts are: chamber formation, organization with cardiac cells, vascularization, and simulation of electrophysiological signals. In particular, since the heart reflects complex factors, it is necessary to develop HOs that can be simulated in depth. In this study, we have created self-organized HOs using human iPSCs, and validated mimicry of cardiac structures such as chamber and epicardium/myocardium and atrium/ventricle-similar areas. Furthermore, mechanical/electrophysiological features were verified through multiple analyzes after inhibition of ion channels. More importantly, the HOs function, due to the cardiovascular characteristics of HOs, was maintained through vascularization after in vivo transplantation. In conclusion, this study has the advantage of being able to easily and closely recapitulate morphological/functional aspects of the heart.-
dc.publisherElsevier-
dc.titleGeneration of human iPSCs derived heart organoids structurally and functionally similar to heart-
dc.title.alternativeGeneration of human iPSCs derived heart organoids structurally and functionally similar to heart-
dc.typeArticle-
dc.citation.titleBiomaterials-
dc.citation.number0-
dc.citation.endPage121860-
dc.citation.startPage121860-
dc.citation.volume290-
dc.contributor.affiliatedAuthorMi-Young Son-
dc.contributor.alternativeName이슬기-
dc.contributor.alternativeName김예지-
dc.contributor.alternativeName손미영-
dc.contributor.alternativeName오민석-
dc.contributor.alternativeName김진-
dc.contributor.alternativeName류보경-
dc.contributor.alternativeName강규리-
dc.contributor.alternativeName백지은-
dc.contributor.alternativeName정구진-
dc.contributor.alternativeName우동호-
dc.contributor.alternativeName김시윤-
dc.contributor.alternativeName정현민-
dc.identifier.bibliographicCitationBiomaterials, vol. 290, pp. 121860-121860-
dc.identifier.doi10.1016/j.biomaterials.2022.121860-
dc.subject.keywordHuman induced pluripotent stem cells-
dc.subject.keywordHeart organoid-
dc.subject.keywordChamber formation-
dc.subject.keywordCardiogenesis-
dc.subject.keywordEpicardium-
dc.subject.keywordMyocardium-
dc.subject.keywordVascularization-
dc.subject.keywordMechanical analysis-
dc.subject.keywordElectrophysiological analysis-
dc.subject.localHuman induced pluripotent stem cell-
dc.subject.localHuman induced pluripotent stem cells-
dc.subject.localhuman-induced pluripotent stem cells-
dc.subject.localhuman induced pluripotent stem cell-
dc.subject.localHeart organoid-
dc.subject.localChamber formation-
dc.subject.localCardiogenesis-
dc.subject.localEpicardium-
dc.subject.localMyocardium-
dc.subject.localvascularization-
dc.subject.localVascularization-
dc.subject.localMechanical analysis-
dc.subject.localElectrophysiological analysis-
dc.description.journalClassY-
Appears in Collections:
Division of Research on National Challenges > Stem Cell Convergenece Research Center > 1. Journal Articles
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