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dc.contributor.authorJunghof, Juliaen
dc.contributor.authorKogure, Yutaen
dc.contributor.authorTian, Yuen
dc.contributor.authorVerdugo-Sivianes, Eva Maríaes
dc.contributor.authorNarita, Megumien
dc.contributor.authorLucena-Cacace, Antonioen
dc.contributor.authorYoshida, Yoshinorien
dc.contributor.alternative小暮, 優太ja
dc.contributor.alternative田, 雨ja
dc.contributor.alternative成田, 恵ja
dc.contributor.alternative吉田, 善紀ja
dc.date.accessioned2022-02-10T08:35:14Z-
dc.date.available2022-02-10T08:35:14Z-
dc.date.issued2022-
dc.identifier.urihttp://hdl.handle.net/2433/267904-
dc.descriptionCDH18は胎児期の心外膜細胞の指標であり胎児心外膜から平滑筋細胞の分化を制御している. 京都大学プレスリリース. 2022-02-09.ja
dc.descriptionUsing stem cells to regenerate the heart. 京都大学プレスリリース. 2022-02-09.en
dc.description.abstractThe epicardium is a mesothelial layer covering the myocardium serving as a progenitor source during cardiac development. The epicardium reactivates upon cardiac injury supporting cardiac repair and regeneration. Fine-tuned balanced signaling regulates cell plasticity and cell-fate decisions of epicardial-derived cells (EPCDs) via epicardial-to-mesenchymal transition (EMT). However, powerful tools to investigate epicardial function, including markers with pivotal roles in developmental signaling, are still lacking. Here, we recapitulated epicardiogenesis using human induced pluripotent stem cells (hiPSCs) and identified type II classical cadherin CDH18 as a biomarker defining lineage specification in human active epicardium. The loss of CDH18 led to the onset of EMT and specific differentiation towards cardiac smooth muscle cells. Furthermore, GATA4 regulated epicardial CDH18 expression. These results highlight the importance of tracing CDH18 expression in hiPSC-derived epicardial cells, providing a model for investigating epicardial function in human development and disease and enabling new possibilities for regenerative medicine.en
dc.language.isoeng-
dc.publisherSpringer Natureen
dc.rights© The Author(s) 2022en
dc.rightsThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder.en
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/-
dc.subjectCell signallingen
dc.subjectRegenerative medicineen
dc.subjectStem-cell differentiationen
dc.subjectTranscriptomicsen
dc.titleCDH18 is a fetal epicardial biomarker regulating differentiation towards vascular smooth muscle cellsen
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitlenpj Regenerative Medicineen
dc.identifier.volume7-
dc.relation.doi10.1038/s41536-022-00207-w-
dc.textversionpublisher-
dc.identifier.artnum14-
dc.addressCenter for iPS Cell Research and Application, Kyoto University; Graduate School of Medicine, Kyoto Universityen
dc.addressCenter for iPS Cell Research and Application, Kyoto University; Research and Development Division, ROHTO Pharmaceutical Co., Ltd.en
dc.addressCenter for iPS Cell Research and Application, Kyoto University; Graduate School of Medicine, Kyoto Universityen
dc.addressInstituto de Biomedicina de Sevilla, IBIS, Hospital Universitario Virgen del Rocío, Universidad de Sevilla, Consejo Superior de Investigaciones Científicas; CIBERONC, Instituto de Salud Carlos IIIes
dc.addressCenter for iPS Cell Research and Application, Kyoto Universityen
dc.addressCenter for iPS Cell Research and Application, Kyoto Universityen
dc.addressCenter for iPS Cell Research and Application, Kyoto Universityen
dc.identifier.pmid35110584-
dc.relation.urlhttps://www.cira.kyoto-u.ac.jp/j/pressrelease/news/220209-150000.html-
dc.relation.urlhttps://www.cira.kyoto-u.ac.jp/e/pressrelease/news/220209-150000.html-
dcterms.accessRightsopen access-
datacite.awardNumber20K17078-
datacite.awardNumber21H02912-
datacite.awardNumber17H04176-
datacite.awardNumber.urihttps://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-20K17078/-
datacite.awardNumber.urihttps://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-21H02912/-
datacite.awardNumber.urihttps://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-17H04176/-
dc.identifier.eissn2057-3995-
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.awardTitleHuman induced pluripotent stem cell derived cardiomyocyte maturation by DNA integrative free-delivery of key regulatorsen
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
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
出現コレクション:学術雑誌掲載論文等

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