Higashigawa M, Ido M, Kuwabara H, Hori H, Ohkubo T, Kawasaki H, Sakurai M, Taniguchi K, Hamazaki M
Department of Pediatrics, Mie University School of Medicine, Japan.
Leuk Res. 1991;15(4):255-62. doi: 10.1016/0145-2126(91)90128-g.
The membrane transport of ara-C and intracellular ara-CTP accumulation were investigated in P388 murine leukemic cells resistant to vincristine (P388/VCR) and its parent cell line. The transport of ara-C in P388/VCR cell line was a 1.4-fold increase at 30 sec compared to that in P388 parent cell line (P less than 0.01). The increase of the transport of ara-C in P388/VCR cell line, however, was not completely abolished by the nucleoside transport inhibitor, nitrobenzylthioinosine (NBTI) to the level in parent cell line. Scatchard analyses revealed that the resistant cells had significantly less NBTI binding sites than the parent cells had. These results suggested that the changes in ara-C transport in P388/VCR cells were due, in part, to increase of NBTI-insensitive transport sites in the membrane. The measurement of the intracellular ara-CTP concentration by high-performance liquid chromatography revealed that the intracellular ara-CTP level in P388/VCR cells was also significantly higher than that in parent cells (1.4-fold, P less than 0.01). As the transport of ara-C is rate limiting at a concentration of 1 microM in the both cell lines, we concluded that the accumulation of ara-CTP in P388/VCR cells might have partially resulted from the enhancement of the ara-C transport.
在对长春新碱耐药的P388小鼠白血病细胞(P388/VCR)及其亲本细胞系中,研究了阿糖胞苷的膜转运及细胞内阿糖胞苷三磷酸(ara - CTP)的蓄积情况。与P388亲本细胞系相比,P388/VCR细胞系中阿糖胞苷在30秒时的转运增加了1.4倍(P < 0.01)。然而,核苷转运抑制剂硝基苄硫肌苷(NBTI)并未将P388/VCR细胞系中阿糖胞苷转运的增加完全消除至亲本细胞系的水平。Scatchard分析显示,耐药细胞的NBTI结合位点明显少于亲本细胞。这些结果表明,P388/VCR细胞中阿糖胞苷转运的变化部分归因于膜中对NBTI不敏感的转运位点的增加。通过高效液相色谱法测定细胞内ara - CTP浓度,结果显示P388/VCR细胞内的ara - CTP水平也显著高于亲本细胞(1.4倍,P < 0.01)。由于在两种细胞系中,1 microM浓度的阿糖胞苷转运是限速步骤,我们得出结论,P388/VCR细胞中ara - CTP的蓄积可能部分是由于阿糖胞苷转运增强所致。