Department of Molecular, Cell and Developmental Biology, Eli and Edythe Broad Center of Regenerative Medicine and Stem Cell Research, University of California, Los Angeles, Los Angeles, CA, 90095, USA.
Division of Reproductive and Developmental Sciences, Oregon National Primate Research Center, Beaverton, OR, 97006, USA.
Nat Commun. 2018 Dec 17;9(1):5339. doi: 10.1038/s41467-018-07740-7.
A major challenge in stem cell differentiation is the availability of bioassays to prove cell types generated in vitro are equivalent to cells in vivo. In the mouse, differentiation of primordial germ cell-like cells (PGCLCs) from pluripotent cells was validated by transplantation, leading to the generation of spermatogenesis and to the birth of offspring. Here we report the use of xenotransplantation (monkey to mouse) and homologous transplantation (monkey to monkey) to validate our in vitro protocol for differentiating male rhesus (r) macaque PGCLCs (rPGCLCs) from induced pluripotent stem cells (riPSCs). Specifically, transplantation of aggregates containing rPGCLCs into mouse and nonhuman primate testicles overcomes a major bottleneck in rPGCLC differentiation. These findings suggest that immature rPGCLCs once transplanted into an adult gonadal niche commit to differentiate towards late rPGCs that initiate epigenetic reprogramming but do not complete the conversion into ENO2-positive spermatogonia.
干细胞分化的一个主要挑战是缺乏生物测定方法来证明体外产生的细胞类型与体内细胞等效。在小鼠中,多能细胞向原始生殖细胞样细胞(PGCLCs)的分化通过移植得到验证,导致了精子发生的产生和后代的诞生。在这里,我们报告了异种移植(猴到鼠)和同源移植(猴到猴)的使用,以验证我们从诱导多能干细胞(riPSCs)体外分化雄性恒河猴(r)猕猴 PGCLCs(rPGCLCs)的体外方案。具体来说,将含有 rPGCLCs 的聚集物移植到小鼠和非人类灵长类动物的睾丸中,克服了 rPGCLC 分化的一个主要瓶颈。这些发现表明,一旦将不成熟的 rPGCLCs 移植到成年性腺巢中,它们就会向晚期 rPGCs 分化,这些 rPGCs 启动表观遗传重编程,但不能完全转化为 ENO2 阳性精原细胞。