Charbord P, Tavian M, Coulombel L, Luton D, San Clemente H, Humeau L, Dieterlen-Lièvre F, Péault B
Institut d'Embryologie Cellulaire et Moléculaire du CNRS et du Collège de France, Nogent-sur-Marne.
C R Seances Soc Biol Fil. 1995;189(4):601-9.
Immunohistochemistry was used to detect markers of the vascular, stromal and hematopoietic cell compartments in the human embryo and early fetus, from 3 to 15 weeks of gestation. CD34 expression was consistently observed at the surface of vascular endothelial cells from off earliest stages tested, at the single exception of embryonic liver blood vessels. Yolk sac hematopoiesis was very transient and limited to primitive erythropoiesis. Clusters of erythroblasts, monocytes and granulocytes appeared from 4 to 5 weeks of gestation in the liver rudiment. The early development of the bone marrow was marked by the rapid invasion, at 8 weeks, of long bone cartilaginous rudiments by CD68+ osteoclast precursors, CD34+ endothelial cells and by preosteoblasts, leading to the development of large vascular sinuses between ossifying trabeculae. Endogenous erythro- and granulopoiesis developed from week 11 in primary logettes always organized around an arteriole, in a loose stromal mesenchymal network established between the media of these arterioles and the sinusal endothelium. Round, hematopoietic CD34+ cells were seen occasionally in yolk sac blood vessels. In the liver they were rare and intermingled as single cells in the hepatocyte cords; strikingly, CD34+ hematopoietic cells could seldom be detected in the developing bone marrow. In contrast, compact clusters of non-endothelial, round CD34+ CD45+ hematopoietic cells were detected, during the 5th week of development, in close association with the ventral wall of the dorsal aorta. These cells exhibit phenotypic and functional characteristics of very primitive hematopoietic progenitors. This observation is in striking correlation with the evidence accumulated in animal models that stem cells for the late embryonic and adult hematopoietic systems develop inside the embryo per se, in the vicinity of the dorsal aorta. We thus suggest that these aorta-associated CD34+ cells, that exhibit an anatomic localization similar to that of the intraembryonic stem cells identified in the avian and murine embryo, are the real stem of human hematopoiesis.
免疫组织化学用于检测妊娠3至15周的人类胚胎和早期胎儿中血管、基质和造血细胞区室的标志物。从最早测试阶段开始,在血管内皮细胞表面始终观察到CD34表达,胚胎肝脏血管是唯一的例外。卵黄囊造血非常短暂,仅限于原始红细胞生成。在妊娠4至5周时,肝脏原基中出现了成红细胞、单核细胞和粒细胞簇。骨髓的早期发育特征是,在8周时,CD68+破骨细胞前体、CD34+内皮细胞和成骨前体细胞迅速侵入长骨软骨原基,导致在骨化小梁之间形成大的血管窦。内源性红细胞生成和粒细胞生成从第11周开始在主要小叶中发展,这些小叶总是围绕小动脉组织,位于这些小动脉中膜和窦状内皮之间建立的疏松基质间充质网络中。在卵黄囊血管中偶尔可见圆形的造血CD34+细胞。在肝脏中,它们很少见,以单个细胞的形式夹杂在肝细胞索中;引人注目的是,在发育中的骨髓中很少能检测到CD34+造血细胞。相比之下,在发育的第5周,检测到紧密聚集的非内皮圆形CD34+ CD45+造血细胞,与背主动脉的腹侧壁密切相关。这些细胞表现出非常原始的造血祖细胞的表型和功能特征。这一观察结果与动物模型中积累的证据惊人地相关,即晚期胚胎和成人造血系统的干细胞在胚胎本身内部、背主动脉附近发育。因此,我们认为这些与主动脉相关的CD34+细胞,其解剖定位与在鸟类和小鼠胚胎中鉴定的胚胎内干细胞相似,是人类造血的真正干细胞。