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Determining the potency of primordial germ cells by injection into early mouse embryos.
Sepulveda-Rincon, Lessly P; Wang, Yi-Fang; Whilding, Chad; Moyon, Benjamin; Ojarikre, Obah A; Maciulyte, Valdone; Hamazaki, Nobuhiko; Hayashi, Katsuhiko; Turner, James M A; Leitch, Harry G.
Affiliation
  • Sepulveda-Rincon LP; Medical Research Council (MRC) Laboratory of Medical Sciences (LMS), London W12 0HS, UK; Institute of Clinical Sciences (ICS), Faculty of Medicine, Imperial College London, London W12 0HS, UK. Electronic address: l.sepulveda-rincon@lms.mrc.ac.uk.
  • Wang YF; Medical Research Council (MRC) Laboratory of Medical Sciences (LMS), London W12 0HS, UK.
  • Whilding C; Medical Research Council (MRC) Laboratory of Medical Sciences (LMS), London W12 0HS, UK.
  • Moyon B; Medical Research Council (MRC) Laboratory of Medical Sciences (LMS), London W12 0HS, UK.
  • Ojarikre OA; Sex Chromosome Biology Laboratory, The Francis Crick Institute, London NW1 1AT, UK.
  • Maciulyte V; Sex Chromosome Biology Laboratory, The Francis Crick Institute, London NW1 1AT, UK.
  • Hamazaki N; Department of Stem Cell Biology and Medicine, Graduate School of Medical Sciences, Kyushu University, Maidashi 3-1-1, Higashi-ku, Fukuoka 812-8582, Japan.
  • Hayashi K; Department of Stem Cell Biology and Medicine, Graduate School of Medical Sciences, Kyushu University, Maidashi 3-1-1, Higashi-ku, Fukuoka 812-8582, Japan; Department of Genome Biology, Graduate School of Medicine, Osaka University, Yamadaoka 2-2, Suita 565-0871, Japan; Graduate School of Frontier Bi
  • Turner JMA; Sex Chromosome Biology Laboratory, The Francis Crick Institute, London NW1 1AT, UK.
  • Leitch HG; Medical Research Council (MRC) Laboratory of Medical Sciences (LMS), London W12 0HS, UK; Institute of Clinical Sciences (ICS), Faculty of Medicine, Imperial College London, London W12 0HS, UK. Electronic address: hleitch@ic.ac.uk.
Dev Cell ; 59(6): 695-704.e5, 2024 Mar 25.
Article in En | MEDLINE | ID: mdl-38359835
ABSTRACT
Primordial germ cells (PGCs) are the earliest precursors of the gametes. During normal development, PGCs only give rise to oocytes or spermatozoa. However, PGCs can acquire pluripotency in vitro by forming embryonic germ (EG) cells and in vivo during teratocarcinogenesis. Classic embryological experiments directly assessed the potency of PGCs by injection into the pre-implantation embryo. As no contribution to embryos or adult mice was observed, PGCs have been described as unipotent. Here, we demonstrate that PGCs injected into 8-cell embryos can initially survive, divide, and contribute to the developing inner cell mass. Apoptosis-deficient PGCs exhibit improved survival in isolated epiblasts and can form naive pluripotent embryonic stem cell lines. However, contribution to the post-implantation embryo is limited, with no functional incorporation observed. In contrast, PGC-like cells show an extensive contribution to mid-gestation chimeras. We thus propose that PGC formation in vivo establishes a latent form of pluripotency that restricts chimera contribution.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pluripotent Stem Cells / Germ Cells Limits: Animals Language: En Journal: Dev Cell Journal subject: EMBRIOLOGIA Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pluripotent Stem Cells / Germ Cells Limits: Animals Language: En Journal: Dev Cell Journal subject: EMBRIOLOGIA Year: 2024 Document type: Article
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