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多药耐药改变P388小鼠淋巴瘤细胞中的多胺摄取:实验与建模方法

Multidrug resistance modifies polyamines uptake in P388 murine lymphoma cells: experimental and modeling approach.

作者信息

Berlaimont V, Bogaerts P, Dubois J, Hanus R, Hanocq M

机构信息

Department of Bioanalytical Chemistry, Toxicology and Applied Physical Chemistry, Université Libre de Bruxelles, Belgium.

出版信息

Biophys Chem. 1999 Mar 29;77(2-3):161-71. doi: 10.1016/s0301-4622(99)00020-4.

Abstract

Polyamines (putrescine, spermidine and spermine) are ubiquitous compounds, essential for cell growth. This paper compares the polyamine transport between sensitive P388 murine lymphoma cells and two multidrug resistant P388 sublines with the assistance of an experimental model. This new model allows the characterisation of the whole polyamines uptake and efflux. Three parameters are identified by the model: two rate constants (K+ for the uptake and K- for the efflux) which are considered as physical constants specific to the transport of one polyamine in one cell type, and Ci(o) which represents the initial intracellular concentration. This model well describes our experimental results of polyamine transport across the P388 cell plasma membrane. Multidrug resistant P388 cells exhibit spermine uptake significantly higher than that of sensitive cells when on the opposite, putrescine enters more rapidly into the sensitive P388 cells. In conclusion, comparison of polyamine transport between sensitive and multidrug resistant P388 phenotypes shows large and significant differences.

摘要

多胺(腐胺、亚精胺和精胺)是普遍存在的化合物,对细胞生长至关重要。本文借助一个实验模型比较了敏感的P388小鼠淋巴瘤细胞与两个多药耐药的P388亚系之间的多胺转运。这个新模型能够对整个多胺的摄取和外排进行表征。该模型确定了三个参数:两个速率常数(摄取的K+和外排的K-),它们被视为特定细胞类型中一种多胺转运的物理常数,以及代表初始细胞内浓度的Ci(o)。该模型很好地描述了我们关于多胺跨P388细胞质膜转运的实验结果。多药耐药的P388细胞的精胺摄取显著高于敏感细胞,而相反,腐胺进入敏感P388细胞的速度更快。总之,敏感和多药耐药的P388表型之间多胺转运的比较显示出巨大且显著的差异。

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