Laurent M, Clémancey-Marcille G, Hollard D
Scand J Haematol. 1980 Mar;24(3):205-12. doi: 10.1111/j.1600-0609.1980.tb01328.x.
Leukaemic human bone marrow and peripheral blood cells were cultured for 25 d in diffusion chambers implanted into cyclophosphamide treated mice. Normal bone marrow cells were cultured simultaneously. These cells were studied both morphologically and functionally (CFU-C). The leukaemic cells behaved heterogeneously, 2 groups being distinguishable in accordance with their initial in vitro growth pattern (1: no growth or microcluster growth. 2: macrocluster growth). Group I showed progressive cellular death with a diminution of granulocytic progenitors and the appearance of a predominantly macrophagic population. This behaviour resembled that of the control group. The initial microcluster growth pattern remained identical throughout the entire culture period. Group 2, after considerable cellular death up to d 5, showed an explosive proliferation of the granulocytic progenitors and incomplete differentiation (up to myelocyte). The initial macrocluster growth pattern remained identical.
将白血病患者的骨髓和外周血细胞在植入经环磷酰胺处理的小鼠体内的扩散小室中培养25天。同时培养正常骨髓细胞。对这些细胞进行了形态学和功能(CFU-C)研究。白血病细胞表现出异质性,根据其初始体外生长模式可分为两组(1:无生长或微集落生长。2:大集落生长)。第一组显示细胞进行性死亡,粒细胞祖细胞减少,主要出现巨噬细胞群体。这种行为与对照组相似。在整个培养期间,初始微集落生长模式保持不变。第二组在第5天之前经历了相当多的细胞死亡,之后粒细胞祖细胞出现爆发性增殖和不完全分化(直至中幼粒细胞)。初始大集落生长模式保持不变。