Ueno Hiroo, Turnbull Brit B, Weissman Irving L
Department of Pathology, Institute of Stem Cell Biology and Regenerative Medicine, Stanford University, Stanford, CA 94305, USA.
Proc Natl Acad Sci U S A. 2009 Jan 6;106(1):175-80. doi: 10.1073/pnas.0810325105. Epub 2008 Dec 19.
During mouse development, primordial germ cells (PGCs) that give rise to the entire germ line are first identified within the proximal epiblast. However, long-term tracing of the fate of the cells has not been done wherein all cells in and around the germ-cell lineage are identified. Also, quantitative estimates of the number of founder PGCs using different models have come up with various numbers. Here, we use tetrachimeric mice to show that the progenitor numbers for the entire germ line in adult testis, and for the initiating embryonic PGCs, are both 4 cells. Although they proliferate to form polyclonal germ-cell populations in fetal and neonatal testes, germ cells that actually contribute to adult spermatogenesis originate from a small number of secondary founder cells that originate in the fetal period. The rest of the "deciduous" germ cells are lost, most likely by apoptosis, before the reproductive period. The second "actual" founder germ cells generally form small numbers of large monoclonal areas in testes by the reproductive period. Our results also demonstrate that there is no contribution of somatic cells to the male germ cell pool during development or in adulthood. These results suggest a model of 2-step oligoclonal development of male germ cells in mice, the second step distinguishing the heritable germ line from cells selected not to participate in forming the next generation.
在小鼠发育过程中,产生整个生殖系的原始生殖细胞(PGCs)最初是在近端上胚层中被识别出来的。然而,尚未对这些细胞的命运进行长期追踪,其中生殖细胞谱系内及其周围的所有细胞都未被识别。此外,使用不同模型对起始PGCs数量的定量估计得出了不同的数字。在这里,我们使用四嵌合小鼠来表明,成年睾丸中整个生殖系的祖细胞数量以及起始胚胎PGCs的祖细胞数量均为4个细胞。尽管它们在胎儿和新生儿睾丸中增殖形成多克隆生殖细胞群体,但实际上对成年精子发生有贡献的生殖细胞起源于少数在胎儿期产生的次级起始细胞。其余的“落叶性”生殖细胞在生殖期之前很可能通过凋亡而丢失。第二个“实际”的起始生殖细胞在生殖期通常在睾丸中形成少量大的单克隆区域。我们的结果还表明,在发育过程或成年期,体细胞对雄性生殖细胞库没有贡献。这些结果提示了小鼠雄性生殖细胞两步寡克隆发育的模型,第二步将可遗传的生殖系与被选择不参与形成下一代的细胞区分开来。