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dc.contributor.authorKasamoto, Manabuen
dc.contributor.authorFunakoshi, Shunsukeen
dc.contributor.authorHatani, Takeshien
dc.contributor.authorOkubo, Chikakoen
dc.contributor.authorNishi, Yoheien
dc.contributor.authorTsujisaka, Yutaen
dc.contributor.authorNishikawa, Misatoen
dc.contributor.authorNarita, Megumien
dc.contributor.authorOhta, Akiraen
dc.contributor.authorKimura, Takeshien
dc.contributor.authorYoshida, Yoshinorien
dc.contributor.alternative笠本, 学ja
dc.contributor.alternative舟越, 俊介ja
dc.contributor.alternative羽溪, 健ja
dc.contributor.alternative大久保, 周子ja
dc.contributor.alternative西, 洋平ja
dc.contributor.alternative辻坂, 勇太ja
dc.contributor.alternative西川, 美里ja
dc.contributor.alternative成田, 恵ja
dc.contributor.alternative太田, 章ja
dc.contributor.alternative木村, 剛ja
dc.contributor.alternative吉田, 善紀ja
dc.date.accessioned2023-08-10T01:50:01Z-
dc.date.available2023-08-10T01:50:01Z-
dc.date.issued2023-08-
dc.identifier.urihttp://hdl.handle.net/2433/284628-
dc.descriptionヒトiPS細胞由来心筋細胞の生着能改善に向けた新しい方法. 京都大学プレスリリース. 2023-07-14.ja
dc.descriptionAm80, a retinoic acid receptor agonist, activates cell cycle in induced cardiomyocytes and enhances heart tissue engraftment. 京都大学プレスリリース. 2023-07-14.en
dc.description.abstractHuman induced pluripotent stem cell-derived (hiPSC) cardiomyocytes are a promising source for regenerative therapy. To realize this therapy, however, their engraftment potential after their injection into the host heart should be improved. Here, we established an efficient method to analyze the cell cycle activity of hiPSC cardiomyocytes using a fluorescence ubiquitination-based cell cycle indicator (FUCCI) system. In vitro high-throughput screening using FUCCI identified a retinoic acid receptor (RAR) agonist, Am80, as an effective cell cycle activator in hiPSC cardiomyocytes. The transplantation of hiPSC cardiomyocytes treated with Am80 before the injection significantly enhanced the engraftment in damaged mouse heart for 6 months. Finally, we revealed that the activation of endogenous Wnt pathways through both RARA and RARB underlies the Am80-mediated cell cycle activation. Collectively, this study highlights an efficient method to activate cell cycle in hiPSC cardiomyocytes by Am80 as a means to increase the graft size after cell transplantation into a damaged heart.en
dc.language.isoeng-
dc.publisherElsevier BVen
dc.rights© 2023 The Authors.en
dc.rightsThis is an open access article under the CC BY-NC-ND license.en
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/-
dc.subjectFUCCIen
dc.subjectCell cycleen
dc.subjectCardiac cell transplantationen
dc.subjecthuman induced pluripotent stem cellsen
dc.subjectcardiomyocyte differentiationen
dc.subjectretinoic aciden
dc.subjecthigh throughput screeningen
dc.titleAm80, a retinoic acid receptor agonist, activates the cardiomyocyte cell cycle and enhances engraftment in the hearten
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitleStem Cell Reportsen
dc.identifier.volume18-
dc.identifier.issue8-
dc.identifier.spage1672-
dc.identifier.epage1685-
dc.relation.doi10.1016/j.stemcr.2023.06.006-
dc.textversionpublisher-
dc.addressCentre for iPS Cell Research and Application, Kyoto University; Department of Cardiovascular Medicine, Kyoto University Hospitalen
dc.addressCentre for iPS Cell Research and Application, Kyoto University; Takeda-CiRA Joint program (T-CiRA)en
dc.addressCentre for iPS Cell Research and Application, Kyoto Universityen
dc.addressCentre for iPS Cell Research and Application, Kyoto Universityen
dc.addressCentre for iPS Cell Research and Application, Kyoto Universityen
dc.addressCentre for iPS Cell Research and Application, Kyoto University; Department of Cardiovascular Medicine, Kyoto University Hospitalen
dc.addressCentre for iPS Cell Research and Application, Kyoto Universityen
dc.addressCentre for iPS Cell Research and Application, Kyoto Universityen
dc.addressCentre for iPS Cell Research and Application, Kyoto Universityen
dc.addressDepartment of Cardiovascular Medicine, Kyoto University Hospitalen
dc.addressCentre for iPS Cell Research and Application, Kyoto University; Takeda-CiRA Joint program (T-CiRA)en
dc.identifier.pmid37451261-
dc.relation.urlhttps://www.cira.kyoto-u.ac.jp/j/pressrelease/news/230714-100000.html-
dc.relation.urlhttps://www.cira.kyoto-u.ac.jp/e/pressrelease/news/230714-100000.html-
dcterms.accessRightsopen access-
datacite.awardNumber17H04176-
datacite.awardNumber21H02912-
datacite.awardNumber.urihttps://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-17H04176/-
datacite.awardNumber.urihttps://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-21H02912/-
dc.identifier.eissn2213-6711-
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.awardTitle多能性幹細胞由来心筋細胞の細胞周期制御のための統合的アプローチja
jpcoar.awardTitle心外膜細胞の増殖分化制御メカニズムの解明とその応用技術の開発ja
出現コレクション:学術雑誌掲載論文等

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