Max-Audit I, Testa U, Kechemir D, Titeux M, Vainchenker W, Rosa R
Blood. 1984 Oct;64(4):930-6.
To further investigate the erythroid nature of the two human erythroleukemia cell lines, K562 and HEL-60, and to define the ontogeny of pyruvate kinase (PK) isozymes (R, M2) in developing human erythroid cells, we have studied the isozymic alterations, if any, during differentiation of these cell lines in vitro and normoblasts isolated from fetal liver in vivo. PK activity of erythroleukemic cell lines was intermediate between that observed in leukocytes and in fetal liver erythroblasts. These cell lines contained a high level of M2-PK, but R-PK was always present, albeit at low concentrations, in all the clones or subclones we studied. Erythroblasts from fetal liver were separated according to density on a Stractan gradient. R-PK levels were nearly constant in the different fractions, whereas M2-PK levels markedly decreased as the erythroblasts became mature and almost completely disappeared in late erythroid cells. Thus, these results clearly demonstrate the erythroid origin of these cell lines.
为了进一步研究两种人类红白血病细胞系K562和HEL - 60的红系性质,并确定丙酮酸激酶(PK)同工酶(R、M2)在人类红系细胞发育过程中的个体发生情况,我们研究了这些细胞系在体外分化过程中以及从体内胎儿肝脏分离的成红细胞中是否存在同工酶改变。红白血病细胞系的PK活性介于白细胞和胎儿肝脏成红细胞中观察到的活性之间。这些细胞系含有高水平的M2 - PK,但在我们研究的所有克隆或亚克隆中,R - PK始终存在,尽管浓度较低。胎儿肝脏的成红细胞根据密度在Stractan梯度上进行分离。不同组分中R - PK水平几乎恒定,而随着成红细胞成熟,M2 - PK水平显著下降,在晚期红系细胞中几乎完全消失。因此,这些结果清楚地证明了这些细胞系的红系起源。