Hinterberger W
Acta Med Austriaca Suppl. 1981;21:1-20.
Myeloid committed stem cells belong to a subpopulation of small nucleated cells, which are defined by their capacity to form colonies of mature myeloid cells in agar-medium. They are termed "Colony forming Unit, CFUC", and such cells are detectable in bone marrow and peripheral blood. Bone marrow cells from 15 control patients with regular myelopoiesis contained 86 +/- 46 CFUC/10(5) bone marrow cells and 23 +/- 14 CFUC/ml blood. In 10 patients with aplastic anemia, only 0-10, 5 CFUC/10(5) BM-cells were found and no CFUC were detectable in the peripheral blood. 17 patients with chronic myeloid leukaemia showed a moderate elevation of bone marrow CFUC (X = 105), while the circulating CFUC were markedly elevated (105-42.000/ml). The circulating CFUC were closely correlated with the number of leukocytes (p less than 0,001). In 12 patients with primary osteomyelofibrosis, the number of circulating CFUC was also (raised (325-22.199/ml) and again, a correlation with the number of leukocytes was observed (p less than 0,05). As, on the other hand, there was no difference in the leukocyte count between the control group and patients with osteomyelosclerosis, the simultaneous assessment of circulating leukocytes and CFUC proves a diagnostic tool. Pancytopenia with a hypercellular bone marrow results from either neoplastic or metabolic alterations of haemopoiesis; in pancytopenia with neoplastic infiltration or transformation, the number of CFUC was lowered, whereas it was slightly elevated in pancytopenia due to metabolic alterations. In patients with acute leukaemia, only a minority of cells was capable of proliferation in vitro. The growth of leukaemic cells in culture, their prolonged survival along with the expression of functional properties may be clinically used for a more subtle classification of blast populations. The data on patients with acute leukaemia indicate, that basic mechanisms of normal blood cell regulation operate in leukaemic haemopoiesis as well.
髓系定向干细胞属于小核细胞亚群,其定义为在琼脂培养基中形成成熟髓系细胞集落的能力。它们被称为“集落形成单位,CFUC”,并且此类细胞在骨髓和外周血中可检测到。15名正常骨髓造血的对照患者的骨髓细胞含有86±46个CFUC/10⁵骨髓细胞和23±14个CFUC/毫升血液。在10名再生障碍性贫血患者中,仅发现0 - 10.5个CFUC/10⁵骨髓细胞,外周血中未检测到CFUC。17名慢性髓性白血病患者显示骨髓CFUC中度升高(X = 105),而循环CFUC显著升高(105 - 42000/毫升)。循环CFUC与白细胞数量密切相关(p < 0.001)。在12名原发性骨髓纤维化患者中,循环CFUC数量也升高(325 - 22199/毫升),并且再次观察到与白细胞数量相关(p < 0.05)。另一方面,由于对照组与骨髓硬化症患者的白细胞计数无差异, 同时评估循环白细胞和CFUC证明是一种诊断工具。全血细胞减少伴骨髓细胞增多是由造血的肿瘤性或代谢性改变引起的;在伴有肿瘤浸润或转化的全血细胞减少中,CFUC数量降低,而在由于代谢改变导致的全血细胞减少中则略有升高。在急性白血病患者中,只有少数细胞能够在体外增殖。白血病细胞在培养中的生长、它们的长期存活以及功能特性的表达可在临床上用于对原始细胞群体进行更精细的分类。急性白血病患者的数据表明,正常血细胞调节的基本机制在白血病造血中也起作用。