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Differentiation of primate primordial germ cell-like cells following transplantation into the adult gonadal niche

机译:植入成年性腺利基后灵长类原始原始生殖细胞样细胞的分化

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摘要

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.
机译:干细胞分化的主要挑战是生物测定方法的有效性,以证明体外产生的细胞类型等同于体内细胞。在小鼠中,通过移植验证了从多能细胞分化出的原始生殖细胞样细胞(PGCLC),从而导致了精子的生成和后代的诞生。在这里,我们报告了异种移植(猴子到小鼠)和同源移植(猴子到猴子)的使用,以验证我们的体外方案,以区分雄性恒河猴(r)猕猴PGCLC(rPGCLC)与诱导多能干细胞(riPSC)。具体而言,将包含rPGCLC的聚集体移植到小鼠和非人类灵长类动物的睾丸中,克服了rPGCLC分化的主要瓶颈。这些发现表明,未成熟的rPGCLCs一旦移植到成年的性腺小生境中,便致力于分化为晚期rPGCs,后者可启动表观遗传重编程,但不能完成向ENO2阳性精原细胞的转化。

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