Drexler H G, Gaedicke G, Minowada J
Exp Hematol. 1986 Sep;14(8):732-7.
The ability of 12-O-tetradecanoylphorbol 13-acetate (TPA) to induce stable phenotypic changes that serve as markers of differentiation was examined in the non-T/non-B leukemia cell lines KM-3 and REH and in the pre-B leukemia cell lines BV-173 and NALM-6. Isoenzymes of the enzymes carboxylic esterase, acid phosphatase, hexosaminidase, and lactate dehydrogenase (LDH), separated by isoelectric focusing on horizontal polyacrylamide thin-layer gels, were used to monitor induced changes. TPA in different concentrations completely or partially inhibited cell proliferation, but had no drug-related cytotoxicity. No increase in the number of nitro-blue-tetrazolium-reducing cells nor adherence to plastic surface was found. In all four cell lines, TPA caused an increase in number and staining intensity of esterase, acid phosphatase, and LDH isoenzymes. The resulting isoenzyme profiles corresponded to those seen at more mature intermediate stages of B-cell proliferation, but did not indicate a terminal differentiation to mature B cells. The loss of the hexosaminidase I isoenzyme, which is a marker of immature hematopoietic cells, was a further indicator of induced maturation. These results demonstrate that while TPA is capable of inducing various immature non-T/non-B and pre-B cell lines to differentiate, the differentiation progression appears to be restricted to intermediate stages, in contrast to the terminal differentiation inducible in myeloid cells.
在非T/非B白血病细胞系KM-3和REH以及前B白血病细胞系BV-173和NALM-6中,研究了12-O-十四烷酰佛波醇-13-乙酸酯(TPA)诱导稳定表型变化作为分化标志物的能力。通过在水平聚丙烯酰胺薄层凝胶上进行等电聚焦分离的羧酸酯酶、酸性磷酸酶、己糖胺酶和乳酸脱氢酶(LDH)的同工酶,用于监测诱导的变化。不同浓度的TPA完全或部分抑制细胞增殖,但无药物相关的细胞毒性。未发现硝基蓝四氮唑还原细胞数量增加或细胞贴壁现象。在所有四种细胞系中,TPA导致酯酶、酸性磷酸酶和LDH同工酶的数量和染色强度增加。所得同工酶谱与B细胞增殖更成熟中间阶段所见的谱相对应,但未表明向成熟B细胞的终末分化。己糖胺酶I同工酶的丧失,这是未成熟造血细胞的标志物,是诱导成熟的进一步指标。这些结果表明,虽然TPA能够诱导各种未成熟的非T/非B和前B细胞系分化,但与髓系细胞中可诱导的终末分化相比,分化进程似乎仅限于中间阶段。