Liu C P, Auerbach R
Center for Developmental Biology, University of Wisconsin, Madison 53706.
Development. 1991 Dec;113(4):1315-23. doi: 10.1242/dev.113.4.1315.
Mature T cells are derived from prethymic stem cells, which arise at one or more extrathymic sites and enter and differentiate in the thymus. The nature of these prethymic stem cells is a critical factor for the formation of the T-cell repertoire. Although the bone marrow of adult mice can provide such stem cells, their origin during murine embryogenesis is still undetermined. Among potential sites for these progenitor cells are the fetal liver and the embryonic yolk sac. Our studies focus on the yolk sac, both because the yolk sac appears earlier than any other proposed site, and because the mammalian yolk sac is the first site of hematopoiesis. Although it has been shown that the yolk sac in midgestation contains stem cells that can enter the thymic rudiment and differentiate toward T-cell lineage, our aim was to analyze the developmental potential of cells in the yolk sac from earlier stages, prior to the formation of the liver and any other internal organ. We show here that the yolk sac from 8- and 9-day embryos (2-9 and 13-19 somites, respectively) can reconstitute alymphoid congenic fetal thymuses and acquire mature T-cell-specific characteristics. Specifically, thymocytes derived from the early embryonic yolk sac can progress to the expression of mature T lymphocyte markers including CD3/T-cell receptor (TCR), CD4 and CD8. In contrast, we have been unable to document the presence of stem cells within the embryo itself at these early stages. These results support the hypothesis that the stem cells capable of populating the thymic rudiment originate in the yolk sac, and that their presence as early as at the 2- to 9-somite stage may indicate that prethymic stem cells found elsewhere in the embryo at later times may have been derived by migration from this extra-embryonic site. Our experimental design does not exclude the possibility of multiple origins of prethymic stem cells of which the yolk sac may provide the first wave of stem cells in addition to other later waves of cells.
成熟T细胞源自胸腺前体细胞,这些细胞产生于一个或多个胸腺外部位,进入胸腺并在其中分化。这些胸腺前体细胞的性质是T细胞库形成的关键因素。虽然成年小鼠的骨髓可以提供此类干细胞,但其在小鼠胚胎发育过程中的起源仍未确定。这些祖细胞的潜在来源包括胎肝和胚胎卵黄囊。我们的研究聚焦于卵黄囊,这是因为卵黄囊比任何其他提出的部位出现得更早,还因为哺乳动物的卵黄囊是造血的第一个部位。尽管已经表明妊娠中期的卵黄囊中含有能够进入胸腺原基并向T细胞谱系分化的干细胞,但我们的目的是分析在肝脏和任何其他内脏器官形成之前更早阶段卵黄囊中细胞的发育潜能。我们在此表明,来自8天和9天胚胎(分别为2 - 9和13 - 19体节)的卵黄囊能够重建无淋巴细胞的同基因胎儿胸腺并获得成熟T细胞特异性特征。具体而言,源自早期胚胎卵黄囊的胸腺细胞能够进展到表达成熟T淋巴细胞标志物,包括CD3/T细胞受体(TCR)、CD4和CD8。相比之下,我们无法证明在这些早期阶段胚胎自身内存在干细胞。这些结果支持了这样的假说,即能够填充胸腺原基的干细胞起源于卵黄囊,并且它们早在2至9体节阶段就存在,这可能表明在胚胎后期在其他部位发现的胸腺前体细胞可能是从这个胚外部位迁移而来的。我们的实验设计并不排除胸腺前体细胞有多种起源的可能性,其中卵黄囊可能除了提供其他后续几批细胞之外,还提供了第一批干细胞。