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.
Medical Research Council (MRC) Laboratory of Medical Sciences (LMS), London W12 0HS, UK.
Dev Cell. 2024 Mar 25;59(6):695-704.e5. doi: 10.1016/j.devcel.2024.01.022. Epub 2024 Feb 14.
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.
原始生殖细胞(PGCs)是配子的最早前体。在正常发育过程中,PGCs 仅产生卵母细胞或精子。然而,PGCs 可以通过形成胚胎生殖(EG)细胞在体外和在畸胎癌发生过程中在体内获得多能性。经典的胚胎学实验通过注射到着床前胚胎中直接评估 PGCs 的潜能。由于没有观察到对胚胎或成年小鼠的贡献,PGCs 被描述为单能性。在这里,我们证明注射到 8 细胞胚胎中的 PGCs 最初可以存活、分裂并有助于发育中的内细胞团。凋亡缺陷的 PGCs 在分离的上胚层中表现出更好的存活能力,并能形成原始多能胚胎干细胞系。然而,对植入后胚胎的贡献是有限的,没有观察到功能整合。相比之下,PGC 样细胞在中期妊娠嵌合体中表现出广泛的贡献。因此,我们提出体内 PGC 的形成建立了一种限制嵌合体贡献的潜在多能性形式。