Caprioli A, Minko K, Drevon C, Eichmann A, Dieterlen-Lièvre F, Jaffredo T
Institut d'Embryologie Cellulaire et Moléculaire du CNRS et du Collège de France, 49 bis av. de la Belle Gabrielle, Nogent s/Marne Cedex, 94736, France.
Dev Biol. 2001 Oct 1;238(1):64-78. doi: 10.1006/dbio.2001.0362.
We recently identified the allantois as a site producing hemopoietic and endothelial cells capable of colonizing the bone marrow of an engrafted host. Here, we report a detailed investigation of some early cytological and molecular processes occurring in the allantoic bud, which are probably involved in the production of angioblasts and hemopoietic cells. We show that the allantois undergoes a program characterized by the prominent expression of several "hemangioblastic" genes in the mesoderm accompanied by other gene patterns in the associated endoderm. VEGF-R2, at least from stage HH17 onward, is expressed and is shortly followed by transcription factors GATA-2, SCL/tal-1, and GATA-1. Blood island-like structures differentiate that contain both CD45(+) cells and cells accumulating hemoglobin; these structures look exactly like blood islands in the yolk sac. This hemopoietic process takes place before the establishment of a vascular network connecting the allantois to the embryo. As far as the endoderm is concerned, GATA-3 mRNA is found in the region where allantois will differentiate before the posterior instestinal portal becomes anatomically distinct. Shortly before the bud grows out, GATA-2 was expressed in the endoderm and, at the same time, the hemangioblastic program became initiated in the mesoderm. GATA-3 is detected at least until E8 and GATA-2 until E3 the latest stage examined for this factor. Using in vitro cultures, we show that allantoic buds, dissected out before the establishment of circulation between the bud and the rest of the embryo, produced erythrocytes of the definitive lineage. Moreover, using heterospecific grafts between chick and quail embryos, we demonstrate that the allantoic vascular network develops from intrinsic progenitors. Taken together, these results extend our earlier findings about the commitment of mesoderm to the endothelial and hemopoietic lineages in the allantois. The detection of a prominent GATA-3 expression restricted to the endoderm of the preallantoic region and allantoic bud, followed by that of GATA-2, is an interesting and novel information, in the context of organ formation and endoderm specification in the emergence of hemopoietic cells.
我们最近确定尿囊是一个产生造血细胞和内皮细胞的部位,这些细胞能够在移植宿主的骨髓中定植。在此,我们报告了对尿囊芽中发生的一些早期细胞学和分子过程的详细研究,这些过程可能与成血管细胞和造血细胞的产生有关。我们发现尿囊经历了一个程序,其特征是中胚层中几个“成血管细胞性”基因的显著表达,同时相关内胚层中也有其他基因模式。至少从HH17期开始,VEGF-R2开始表达,随后不久转录因子GATA-2、SCL/tal-1和GATA-1也开始表达。出现了血岛样结构,其中既含有CD45(+)细胞,也含有积累血红蛋白的细胞;这些结构与卵黄囊中的血岛完全相似。这种造血过程发生在连接尿囊和胚胎的血管网络建立之前。就内胚层而言,在尿囊分化区域发现了GATA-3 mRNA,此时后肠门在解剖学上尚未明显分化。在芽长出前不久,GATA-2在内胚层中表达,与此同时,中胚层中开始了成血管细胞程序。至少在E8期之前都能检测到GATA-3,而GATA-2至少在E3期之前都能检测到,这是对该因子检测的最晚阶段。通过体外培养,我们发现,在尿囊芽与胚胎其他部分之间建立循环之前分离出的尿囊芽,能够产生定型谱系的红细胞。此外,通过鸡胚和鹌鹑胚之间的异种移植,我们证明尿囊血管网络由内在祖细胞发育而来。综上所述,这些结果扩展了我们之前关于中胚层在尿囊中向内皮和造血谱系定向分化的研究发现。在造血细胞出现过程中的器官形成和内胚层特化背景下,检测到仅限于尿囊前区和尿囊芽内胚层的显著GATA-3表达,随后是GATA-2的表达,这是一个有趣且新颖的信息。