Chow M, Rubin H
Department of Molecular and Cell Biology, University of California, Berkeley 94720-3206, USA.
In Vitro Cell Dev Biol Anim. 1999 Jul-Aug;35(7):394-402. doi: 10.1007/s11626-999-0114-5.
A quantitative study was made of the cytotoxicity of methotrexate (MTX) for nontransformed and transformed NIH 3T3 cells in the presence and absence of leucovorin. The study was preceded by an analysis of the growth rates of the cells at low and high population density combined with low and high concentrations of calf serum (CS). The reduced maximal growth rates of the transformed cells at low population densities relative to the nontransformed cells reinforced earlier evidence that heritable damage involving chromosome aberrations drives the process of transformation. When small numbers of transformed cells are cocultured with a large excess of nontransformed cells in the assay for transformed foci, the transformed cells were more readily killed by MTX than the nontransformed cells. The selectivity was increased when leucovorin (folinic acid) was present in the medium. The selective killing of the transformed cells actively multiplying in foci was most pronounced when the background of nontransformed cells had become confluent and their growth was inhibited. However, selectivity has also been demonstrated when transformed and nontransformed cells are growing at their maximum rates at low density despite the lower growth rate of the transformed cells under these conditions. The sensitivity of transformed cells in pure culture to MTX was lower during the first 3 d of subculture than in the following 6 d but decreased to zero a few d after net growth had ceased. The nontransformed cells were more susceptible to killing by MTX in Dulbecco's modified Eagle's medium (DMEM) than in MCDB 402, but the transformed cells were sensitive to MTX in both media. The high selectivity of MTX for transformed over nontransformed cells in MCDB 402 results from the presence of 1.0 microM leucovorin (5-formyltetrahydrofolate), a reduced form of the folic acid present in most other culture media. When leucovorin was added to DMEM with its high concentration of folic acid, the resistance to MTX of both nontransformed and transformed cells was greatly increased, but the selectivity of MTX for transformed cells was almost entirely lost. The results indicate that leucovorin protects nontransformed cells against concentrations of MTX that kill transformed cells, but the protection is dependent on the relative amounts of leucovorin to folic acid in the medium. The relative sensitivities of transformed and nontransformed cells in our system to MTX when both cell types are exhibiting their characteristic differential in growth behavior is similar to that described for tumor and normal cells in vivo. Since the unregulated growth behavior of the transformed, tumor-producing cells is efficiently and quantitatively measured in this system, it can be used to develop general principles of treatment and resolve questions of cytotoxic mechanism.
在有和没有亚叶酸的情况下,对甲氨蝶呤(MTX)对未转化和转化的NIH 3T3细胞的细胞毒性进行了定量研究。该研究之前分析了低和高细胞密度以及低和高浓度小牛血清(CS)条件下细胞的生长速率。与未转化细胞相比,转化细胞在低细胞密度下最大生长速率降低,这进一步证明了涉及染色体畸变的遗传性损伤驱动了转化过程。在转化灶检测中,当少量转化细胞与大量未转化细胞共培养时,转化细胞比未转化细胞更容易被MTX杀死。当培养基中存在亚叶酸(甲酰四氢叶酸)时,这种选择性增加。当未转化细胞背景汇合且生长受到抑制时,对在灶中活跃增殖的转化细胞的选择性杀伤最为明显。然而,当转化细胞和未转化细胞在低密度下以最大速率生长时(尽管在此条件下转化细胞生长速率较低),也证明了选择性。在传代培养的前3天,纯培养中的转化细胞对MTX的敏感性低于接下来的6天,但在净生长停止几天后降至零。在杜氏改良 Eagle 培养基(DMEM)中,未转化细胞比在MCDB 402中更容易被MTX杀死,但转化细胞在两种培养基中对MTX都敏感。MTX在MCDB 402中对转化细胞比对未转化细胞具有高选择性,这是由于存在1.0 microM亚叶酸(5-甲酰四氢叶酸),这是大多数其他培养基中存在的叶酸的还原形式。当将亚叶酸添加到叶酸浓度高的DMEM中时,未转化和转化细胞对MTX的抗性都大大增加,但MTX对转化细胞的选择性几乎完全丧失。结果表明,亚叶酸可保护未转化细胞免受杀死转化细胞的MTX浓度的影响,但这种保护取决于培养基中亚叶酸与叶酸的相对量。当两种细胞类型都表现出其特征性的生长行为差异时,我们系统中转化细胞和未转化细胞对MTX的相对敏感性与体内肿瘤细胞和正常细胞的情况相似。由于在该系统中可以有效且定量地测量转化的肿瘤产生细胞的不受调控的生长行为,因此它可用于制定一般治疗原则并解决细胞毒性机制问题。