Scher W, Hellinger N, Waxman S
Exp Hematol. 1985 Jan;13(1):36-43.
Several protease preparations of varied specificity increased hemoglobin levels in K562 cells. These are the first enzymes shown to stimulate this process in these cells. Hemin, at a concentration at which it did not act as a potent inducer of hemoglobin production, was found to synergistically stimulate induction by proteases. As seen in some other cell types, six different protease preparations also stimulated K562 cell yield. Hemin did not enhance the protease stimulation of cell yield, but was, instead, slightly inhibitory. Trypsin was one of the most potent inducers of the proteases tested. A combination of trypsin with a "synergistic" concentration of hemin did not decrease the size of K562 cells during induction of hemoglobin production, suggesting that these cells were not irreversibly differentiated nor induced to terminal cell division by this treatment. This was supported, although not proven, by an assay that demonstrated no progressive decrease in the rate of cell multiplication associated with the induction of hemoglobin synthesis.
几种具有不同特异性的蛋白酶制剂可提高K562细胞中的血红蛋白水平。这些是首次显示能在这些细胞中刺激这一过程的酶。发现血红素在其不作为血红蛋白产生的强效诱导剂的浓度下,能协同刺激蛋白酶的诱导作用。正如在其他一些细胞类型中所见,六种不同的蛋白酶制剂也能刺激K562细胞的产量。血红素并未增强蛋白酶对细胞产量的刺激作用,反而有轻微抑制作用。胰蛋白酶是所测试的蛋白酶中最有效的诱导剂之一。在诱导血红蛋白产生过程中,胰蛋白酶与“协同”浓度的血红素组合并未减小K562细胞的大小,这表明这些细胞未因这种处理而发生不可逆分化,也未被诱导进行终末细胞分裂。一项显示与血红蛋白合成诱导相关的细胞增殖速率没有逐渐下降的测定法支持了这一点,尽管尚未得到证实。