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dc.contributor.authorKinoshita, M
dc.contributor.authorKobayashi, T
dc.contributor.authorPlanells, B
dc.contributor.authorKlisch, D
dc.contributor.authorSpindlow, D
dc.contributor.authorMasaki, H
dc.contributor.authorBornelöv, S
dc.contributor.authorStirparo, GG
dc.contributor.authorMatsunari, H
dc.contributor.authorUchikura, A
dc.contributor.authorLamas-Toranzo, I
dc.contributor.authorNichols, J
dc.contributor.authorNakauchi, H
dc.contributor.authorNagashima, H
dc.contributor.authorAlberio, R
dc.contributor.authorSmith, A
dc.date.accessioned2022-03-11T09:17:31Z
dc.date.issued2021-12-07
dc.date.updated2022-03-10T17:52:27Z
dc.description.abstractDespite four decades of effort, robust propagation of pluripotent stem cells from livestock animals remains challenging. The requirements for self-renewal are unclear and the relationship of cultured stem cells to pluripotent cells resident in the embryo uncertain. Here, we avoided using feeder cells or serum factors to provide a defined culture microenvironment. We show that the combination of activin A, fibroblast growth factor and the Wnt inhibitor XAV939 (AFX) supports establishment and continuous expansion of pluripotent stem cell lines from porcine, ovine and bovine embryos. Germ layer differentiation was evident in teratomas and readily induced in vitro. Global transcriptome analyses highlighted commonality in transcription factor expression across the three species, while global comparison with porcine embryo stages showed proximity to bilaminar disc epiblast. Clonal genetic manipulation and gene targeting were exemplified in porcine stem cells. We further demonstrated that genetically modified AFX stem cells gave rise to cloned porcine foetuses by nuclear transfer. In summary, for major livestock mammals, pluripotent stem cells related to the formative embryonic disc are reliably established using a common and defined signalling environment.en_GB
dc.description.sponsorshipBiotechnology and Biological Sciences Research Councilen_GB
dc.description.sponsorshipBiotechnology and Biological Sciences Research Councilen_GB
dc.description.sponsorshipEuropean Research Councilen_GB
dc.description.sponsorshipMedical Research Councilen_GB
dc.description.sponsorshipMedical Research Councilen_GB
dc.description.sponsorshipJapan Society for the Promotion of Scienceen_GB
dc.description.sponsorshipJapan Society for the Promotion of Scienceen_GB
dc.description.sponsorshipJapan Agency for Medical Research and Developmenten_GB
dc.description.sponsorshipJapan Agency for Medical Research and Developmenten_GB
dc.description.sponsorshipWellcome Trusten_GB
dc.description.sponsorshipMedical Research Councilen_GB
dc.identifier.citationVol. 148 No. 23, article 199901.en_GB
dc.identifier.doihttps://doi.org/10.1242/dev.199901
dc.identifier.grantnumberBB/P009867/1en_GB
dc.identifier.grantnumberBB/S000178/1en_GB
dc.identifier.grantnumber835312en_GB
dc.identifier.grantnumberMR/S020845/1en_GB
dc.identifier.grantnumberG1100526/1en_GB
dc.identifier.grantnumber18H05544en_GB
dc.identifier.grantnumber20H03167en_GB
dc.identifier.grantnumberJP18bm0704022en_GB
dc.identifier.grantnumber21bm1004002h0002en_GB
dc.identifier.grantnumber203151/Z/16/Zen_GB
dc.identifier.grantnumberMC_PC_17230en_GB
dc.identifier.urihttp://hdl.handle.net/10871/129015
dc.identifierORCID: 0000-0002-3029-4682 (Smith, Austin)
dc.identifierScopusID: 8084280500 (Smith, Austin)
dc.language.isoenen_GB
dc.publisherPalgrave Macmillan/Society for International Developmenten_GB
dc.rights.embargoreasonUnder embargo until 7 December 2022 in compliance with publisher policyen_GB
dc.rights© 2021. Published by The Company of Biologists Ltd This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.en_GB
dc.subjectEmbryonic stem cellsen_GB
dc.subjectEpiblasten_GB
dc.subjectMammalian embryoen_GB
dc.subjectNuclear transferen_GB
dc.subjectPluripotencyen_GB
dc.subjectSelf-renewalen_GB
dc.titlePluripotent stem cells related to embryonic disc exhibit common self-renewal requirements in diverse livestock speciesen_GB
dc.typeArticleen_GB
dc.date.available2022-03-11T09:17:31Z
dc.identifier.issn1011-6370
dc.descriptionThis is the author accepted manuscript. The final version is available from Palgrave Macmillan via the DOI in this record en_GB
dc.descriptionData Availability: RNA-seq data generated in this study are deposited in Gene Expression Omnibus under accession number GSE172420 (reviewer token wjevsgycnnafbub).en_GB
dc.identifier.eissn1461-7072
dc.identifier.journalDevelopmenten_GB
dc.relation.ispartofDevelopment
dc.rights.urihttps://creativecommons.org/licenses/by/4.0en_GB
dcterms.dateAccepted2021-10-26
rioxxterms.versionAMen_GB
rioxxterms.licenseref.startdate2021-10-26
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2022-03-10T17:53:09Z
refterms.versionFCDAM
refterms.panelAen_GB
refterms.dateFirstOnline2021-12-07


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© 2021. Published by The Company of Biologists Ltd
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
Except where otherwise noted, this item's licence is described as © 2021. Published by The Company of Biologists Ltd This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.