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Isolation of primitive mouse extraembryonic endoderm (pXEN) stem cell lines

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dc.contributor.authorZhong, Yixiang-
dc.contributor.authorChoi, Taewoong-
dc.contributor.authorKim, Minjae-
dc.contributor.authorJung, Kyoung Hwa-
dc.contributor.authorChai, Young Gyu-
dc.contributor.authorBinas, Bert-
dc.date.accessioned2021-06-22T11:42:51Z-
dc.date.available2021-06-22T11:42:51Z-
dc.date.created2021-01-21-
dc.date.issued2018-07-
dc.identifier.issn1873-5061-
dc.identifier.urihttps://scholarworks.bwise.kr/erica/handle/2021.sw.erica/5795-
dc.description.abstractMouse blastocysts contain the committed precursors of the extraembryonic endoderm (ExEn), which express the key transcription factor Oct4, depend on LIF/LIF-like factor-driven Jak/Stat signaling, and initially exhibit lineage plasticity. Previously described rat blastocyst-derived ExEn precursor-like cell lines (XENP cells/HypoSCs) also show these features, but equivalent mouse blastocyst-derived cell lines are lacking. We now present mouse blastocyst-derived cell lines, named primitive XEN (pXEN) cells, which share these and additional characteristics with the XENP cells/HypoSCs, but not with previously known mouse blastocyst-derived XEN cell lines. Otherwise, pXEN cells are highly similar to XEN cells by morphology, lineage-intrinsic differentiation potential, and multi-gene expression profile, although the pXEN cell profile correlates better with the blastocyst stage. Finally, we show that pXEN cells easily convert into XEN-like cells but not vice versa. The findings indicate that (i) pXEN cells are more representative than XEN cells of the blastocyst stage; (ii) mouse pXEN, rather than XEN, cells are homologs of rat XENP cells/HypoSCs, which we propose to call rat pXEN cells.-
dc.language영어-
dc.language.isoen-
dc.publisherELSEVIER SCIENCE BV-
dc.titleIsolation of primitive mouse extraembryonic endoderm (pXEN) stem cell lines-
dc.typeArticle-
dc.contributor.affiliatedAuthorBinas, Bert-
dc.identifier.doi10.1016/j.scr.2018.05.008-
dc.identifier.scopusid2-s2.0-85047456600-
dc.identifier.wosid000438786600013-
dc.identifier.bibliographicCitationSTEM CELL RESEARCH, v.30, pp.100 - 112-
dc.relation.isPartOfSTEM CELL RESEARCH-
dc.citation.titleSTEM CELL RESEARCH-
dc.citation.volume30-
dc.citation.startPage100-
dc.citation.endPage112-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaCell Biology-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryCell & Tissue Engineering-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryCell Biology-
dc.subject.keywordPlusCULTURE-CONDITIONS SUPPORT-
dc.subject.keywordPlusSELF-RENEWAL-
dc.subject.keywordPlusXEN CELLS-
dc.subject.keywordPlusTRANSCRIPTION FACTOR-
dc.subject.keywordPlusVISCERAL ENDODERM-
dc.subject.keywordPlusBONE-MARROW-
dc.subject.keywordPlusBLASTOCYST-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusEMBRYOS-
dc.subject.keywordPlusOCT4-
dc.subject.keywordAuthorStem cells-
dc.subject.keywordAuthorBlastocyst-
dc.subject.keywordAuthorMice-
dc.subject.keywordAuthorRats-
dc.subject.keywordAuthorExtraembryonic endoderm-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S1873506118301260?via%3Dihub-
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COLLEGE OF SCIENCE AND CONVERGENCE TECHNOLOGY > DEPARTMENT OF MOLECULAR & LIFE SCIENCE > 1. Journal Articles

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