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Epigenetic Regulation of Cardiomyocyte Differentiation from Embryonic and Induced Pluripotent Stem Cells

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dc.contributor.authorKim, Yong-Jin-
dc.contributor.authorTamadon, Amin-
dc.contributor.authorKim, Yoon-Young-
dc.contributor.authorKang, Byeong-Cheol-
dc.contributor.authorKu, Seung-Yup-
dc.date.accessioned2022-02-26T12:40:50Z-
dc.date.available2022-02-26T12:40:50Z-
dc.date.created2022-02-07-
dc.date.issued2021-08-
dc.identifier.issn1661-6596-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/137014-
dc.description.abstractWith the intent to achieve the best modalities for myocardial cell therapy, different cell types are being evaluated as potent sources for differentiation into cardiomyocytes. Embryonic stem cells and induced pluripotent stem cells have great potential for future progress in the treatment of myocardial diseases. We reviewed aspects of epigenetic mechanisms that play a role in the differentiation of these cells into cardiomyocytes. Cardiomyocytes proliferate during fetal life, and after birth, they undergo permanent terminal differentiation. Upregulation of cardiac-specific genes in adults induces hypertrophy due to terminal differentiation. The repression or expression of these genes is controlled by chromatin structural and epigenetic changes. However, few studies have reviewed and analyzed the epigenetic aspects of the differentiation of embryonic stem cells and induced pluripotent stem cells into cardiac lineage cells. In this review, we focus on the current knowledge of epigenetic regulation of cardiomyocyte proliferation and differentiation from embryonic and induced pluripotent stem cells through histone modification and microRNAs, the maintenance of pluripotency, and its alteration during cardiac lineage differentiation.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherMDPI-
dc.subjectPROMOTES CARDIAC DIFFERENTIATION-
dc.subjectCHROMATIN-REMODELING COMPLEXES-
dc.subjectHISTONE H3 LYSINE-27-
dc.subjectGENE-EXPRESSION-
dc.subjectDNA METHYLATION-
dc.subjectDEVELOPMENTAL REGULATORS-
dc.subjectTHERAPEUTIC-EFFICACY-
dc.subjectTRANSCRIPTION FACTOR-
dc.subjectSMALL-MOLECULE-
dc.subjectTARGET GENES-
dc.titleEpigenetic Regulation of Cardiomyocyte Differentiation from Embryonic and Induced Pluripotent Stem Cells-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Yong-Jin-
dc.identifier.doi10.3390/ijms22168599-
dc.identifier.scopusid2-s2.0-85112268584-
dc.identifier.wosid000689170700001-
dc.identifier.bibliographicCitationINTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, v.22, no.16-
dc.relation.isPartOfINTERNATIONAL JOURNAL OF MOLECULAR SCIENCES-
dc.citation.titleINTERNATIONAL JOURNAL OF MOLECULAR SCIENCES-
dc.citation.volume22-
dc.citation.number16-
dc.type.rimsART-
dc.type.docTypeReview-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusCHROMATIN-REMODELING COMPLEXES-
dc.subject.keywordPlusDEVELOPMENTAL REGULATORS-
dc.subject.keywordPlusDNA METHYLATION-
dc.subject.keywordPlusGENE-EXPRESSION-
dc.subject.keywordPlusHISTONE H3 LYSINE-27-
dc.subject.keywordPlusPROMOTES CARDIAC DIFFERENTIATION-
dc.subject.keywordPlusSMALL-MOLECULE-
dc.subject.keywordPlusTARGET GENES-
dc.subject.keywordPlusTHERAPEUTIC-EFFICACY-
dc.subject.keywordPlusTRANSCRIPTION FACTOR-
dc.subject.keywordAuthorcardiomyocyte-
dc.subject.keywordAuthordifferentiation-
dc.subject.keywordAuthorembryonic stem cell-
dc.subject.keywordAuthorepigenetic markers-
dc.subject.keywordAuthorinduced pluripotent stem cell-
dc.subject.keywordAuthorproliferation-
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