Péault B
Institut d'Embryologie, Cellulaire et Moléculaire du CNRS, Collège de France, Nogent-sur-Marne.
C R Acad Sci III. 1993 Sep;316(9):902-8.
Human fetal blood tissues implanted in the SCID immuno-deficient mouse are tolerated and develop considerably. The bone marrow maintains its autonomous hematopoietic function for several months. Conversely, thymic lymphopoiesis can continue over the long term only in the presence of an appropriate source of stem cells. This in vivo replica of the human blood system can be used to test the hematogenic abilities of candidate populations of human hematopoietic stem cells, as suggested by the hematogenic reconstitution of human thymus and marrow in SCID mice obtained from purified CD34+ precursors. In the same model, hematogenic activity of CD34+ cells was limited to the sub-population of these precursors coexpressing the antigen Thy-1. These results, combined with those of in vitro analyses, suggest that the population of CD34+ Thy-1+ components of fetal liver and of the bone marrow is extremely rich in human hematopoietic stem cells.
植入重症联合免疫缺陷(SCID)小鼠体内的人类胎儿血液组织能够被耐受并得到显著发育。骨髓在数月内维持其自主造血功能。相反,只有在存在合适的干细胞来源时,胸腺淋巴细胞生成才能长期持续。如从纯化的CD34 +前体细胞获得的SCID小鼠中人类胸腺和骨髓的造血重建所示,这种人类血液系统的体内复制品可用于测试人类造血干细胞候选群体的造血能力。在同一模型中,CD34 +细胞的造血活性仅限于这些共表达抗原Thy-1的前体亚群。这些结果与体外分析结果相结合,表明胎儿肝脏和骨髓中CD34 + Thy-1 +成分群体富含人类造血干细胞。