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Defined Conditions Control the Morphological Dualism of Rat Primitive Extraembryonic Endoderm Stem Cells

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dc.contributor.authorWang, Xiaoqiong-
dc.contributor.authorKim, Minjae-
dc.contributor.authorJung, Kyoung Hwa-
dc.contributor.authorChai, Young Gyu-
dc.contributor.authorBinas, Bert-
dc.date.accessioned2023-12-08T09:33:40Z-
dc.date.available2023-12-08T09:33:40Z-
dc.date.issued2023-12-
dc.identifier.issn1547-3287-
dc.identifier.issn1557-8534-
dc.identifier.urihttps://scholarworks.bwise.kr/erica/handle/2021.sw.erica/115955-
dc.description.abstractRat primitive extraembryonic endoderm (pXEN) stem cell lines indefinitely preserve the characteristic features of the early extraembryonic endoderm (ExEn) in vitro, but require unknown serum factors and exhibit a hybrid (mesenchymal-epithelial) phenotype. We report two chemically defined conditions that differ by the addition of the cytokine leukemia inhibitory factor (Lif) and the b-catenin-stabilizing drug Chir99021, and enable permanent self-renewal as mesenchymal and epithelial morphotypes, respectively. The morphotypes are interconvertible and equipotent, as shown by the formation of well-differentiated organoids. Surprisingly, the proliferation of both morphotypes requires Lif-type Gp130/Stat3 signaling (autocrine in the absence of added Lif) and noncanonical Wnt signaling (autocrine). In addition, the epithelial version requires b-catenin for proliferation and morphology. Interestingly, the mesenchymal cells also express key epithelial markers, but those are improperly structured and/or not functional, indicating a primed state. These results provide an improved platform for studying the proliferation and plasticity of the early ExEn, which occurs in mesenchymal and epithelial forms in vivo. © 2023 Mary Ann Liebert Inc.. All rights reserved.-
dc.format.extent16-
dc.language영어-
dc.language.isoENG-
dc.publisherMary Ann Liebert Inc.-
dc.titleDefined Conditions Control the Morphological Dualism of Rat Primitive Extraembryonic Endoderm Stem Cells-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1089/scd.2023.0187-
dc.identifier.scopusid2-s2.0-85177242239-
dc.identifier.wosid001112552200002-
dc.identifier.bibliographicCitationStem Cells and Development, v.32, no.23-24, pp 1 - 16-
dc.citation.titleStem Cells and Development-
dc.citation.volume32-
dc.citation.number23-24-
dc.citation.startPage1-
dc.citation.endPage16-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaCell Biology-
dc.relation.journalResearchAreaHematology-
dc.relation.journalResearchAreaResearch & Experimental Medicine-
dc.relation.journalResearchAreaTransplantation-
dc.relation.journalWebOfScienceCategoryCell & Tissue Engineering-
dc.relation.journalWebOfScienceCategoryHematology-
dc.relation.journalWebOfScienceCategoryMedicine, Research & Experimental-
dc.relation.journalWebOfScienceCategoryTransplantation-
dc.subject.keywordPlusXEN CELLS-
dc.subject.keywordPlusVISCERAL ENDODERM-
dc.subject.keywordPlusDIFFERENTIATION-
dc.subject.keywordPlusPLURIPOTENCY-
dc.subject.keywordAuthorchemically defined culture-
dc.subject.keywordAuthorEMT/MET-
dc.subject.keywordAuthorextraembryonic endoderm-
dc.subject.keywordAuthorrat-
dc.subject.keywordAuthorstem cells-
dc.identifier.urlhttps://www.liebertpub.com/doi/10.1089/scd.2023.0187-
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