| Literature DB >> 33382978 |
Irène Aksoy1, Cloé Rognard2, Anaïs Moulin2, Guillaume Marcy2, Etienne Masfaraud2, Florence Wianny2, Véronique Cortay2, Angèle Bellemin-Ménard2, Nathalie Doerflinger2, Manon Dirheimer2, Chloé Mayère2, Pierre-Yves Bourillot2, Cian Lynch3, Olivier Raineteau2, Thierry Joly4, Colette Dehay2, Manuel Serrano3, Marielle Afanassieff2, Pierre Savatier5.
Abstract
After reprogramming to naive pluripotency, human pluripotent stem cells (PSCs) still exhibit very low ability to make interspecies chimeras. Whether this is because they are inherently devoid of the attributes of chimeric competency or because naive PSCs cannot colonize embryos from distant species remains to be elucidated. Here, we have used different types of mouse, human, and rhesus monkey naive PSCs and analyzed their ability to colonize rabbit and cynomolgus monkey embryos. Mouse embryonic stem cells (ESCs) remained mitotically active and efficiently colonized host embryos. In contrast, primate naive PSCs colonized host embryos with much lower efficiency. Unlike mouse ESCs, they slowed DNA replication after dissociation and, after injection into host embryos, they stalled in the G1 phase and differentiated prematurely, regardless of host species. We conclude that human and non-human primate naive PSCs do not efficiently make chimeras because they are inherently unfit to remain mitotically active during colonization.Entities:
Keywords: BCL2; human; interspecies chimera; macaque monkey; mouse; naive pluripotency; non-human primate; pluripotent stem cells; rabbit; reprogramming
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Year: 2020 PMID: 33382978 PMCID: PMC7815945 DOI: 10.1016/j.stemcr.2020.12.004
Source DB: PubMed Journal: Stem Cell Reports ISSN: 2213-6711 Impact factor: 7.765