Verfaillie C M, Miller W J, Boylan K, McGlave P B
Department of Medicine, University of Minnesota Medical School, Minneapolis 55455.
Blood. 1992 Feb 15;79(4):1003-10.
Chronic myelogenous leukemia (CML) is a lethal malignancy of the human hematopoietic stem cell. Here we report that coexistent benign, primitive hematopoietic progenitors can be distinguished from their malignant counterparts in CML bone marrow by differences in cell surface antigen expression. Selection of bone marrow cells expressing the CD34 antigen but lacking the HLA-DR antigen results in recovery of small lymphocyte-like blasts, which initiate and sustain production of myeloid clonogenic progeny in vitro. Secondary clonogenic cells derived at week 1, 5, and 8 from long-term bone marrow cultures (LTBMCs) initiated with primitive progenitors, which lack HLA-DR antigens, exhibit neither the Philadelphia chromosome (Ph1) nor the corresponding bcr/abl mRNA characteristic of CML. In contrast, clonogenic cells recovered at week 1, 5, and 8 from LTBMCs initiated with the CML HLA-DR+ population contain Ph1 and express bcr/abl mRNA. This observation indicates that it may be possible to select a population of viable, exclusively benign hematopoietic stem cells from CML bone marrow capable of repopulating the hematopoietic compartment following autologous bone marrow transplantation.
慢性粒细胞白血病(CML)是一种人类造血干细胞的致命恶性肿瘤。在此我们报告,通过细胞表面抗原表达的差异,可以在CML骨髓中将共存的良性原始造血祖细胞与其恶性对应物区分开来。选择表达CD34抗原但缺乏HLA-DR抗原的骨髓细胞,可获得小淋巴细胞样原始细胞,这些细胞在体外启动并维持髓系克隆形成后代的产生。从缺乏HLA-DR抗原的原始祖细胞起始的长期骨髓培养(LTBMC)在第1、5和8周衍生的二代克隆形成细胞,既不显示费城染色体(Ph1),也不具有CML相应的bcr/abl mRNA特征。相反,从以CML HLA-DR+群体起始的LTBMC在第1、5和8周回收的克隆形成细胞含有Ph1并表达bcr/abl mRNA。这一观察结果表明,有可能从CML骨髓中选择一群有活力的、完全良性的造血干细胞,它们能够在自体骨髓移植后重新填充造血系统。