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聚(6-硫代肌苷酸)和6-巯基嘌呤处理的L1210细胞的比较动力学

Comparative kinetics of poly(6-thioinosinic acid) and 6-mercaptopurine treated L1210 cells.

作者信息

Tomasovic S P, Higashikubo R, Cohen A M, Broom A D

出版信息

Cytometry. 1982 Jul;3(1):48-54. doi: 10.1002/cyto.990030111.

Abstract

Poly(6-thioinosinic acid), poly(s6I), a synthetic polynucleotide shown to inhibit L1210 ascites growth in vivo, was compared with 6-mercaptopurine (6-MP) for their effects on cellular kinetics of L1210 cells in vitro. These kinetic perturbations were monitored by changes in growth rates, cell volumes and cell-cycle distributions. At equimolar exposure doses (based on molar concentration of purine bases), 0.1 mM poly(s6I) was more effective than 6-MP in reducing growth rate and total cell number. A 20-fold increase in the 6-MP exposure dose (to 2 mM) was required to reduce total cell number similar to 0.1 mM poly(s6I). Concomitant determination of Coulter volume distributions of treated cell populations indicated 0.1 mM poly(s6I) increased the mean population volume more than either concentration of 6-MP. Cell-cycle distributions obtained by flow cytometry showed that, simultaneously with the increase in mean population volume, poly(s6I) exposure caused a decrease of cells in G1 and S and a pronounced accumulation of cells in G2. Treatment with 6-MP caused similar cell-cycle redistributions but always less than for poly(s6I). Flow sorting of these redistributed populations indicated the increase in mean population volume during treatment with 0.1 mM poly(s6I) was almost equally due to an increased percentage of G2 cells and to an increased volume of cells with the G2 DNA content. However, with 0.1 mM 6-MP, increased volume of G2 cells was predominant. Although poly(s6I) was synthesized in an attempt to develop more effective delivery forms of biologically active compounds like 6-MP and it has close structural similarities to 6-MP, its mechanism of action is unknown.

摘要

聚(6-硫代肌苷酸),即聚(s6I),是一种在体内可抑制L1210腹水瘤生长的合成多核苷酸。将其与6-巯基嘌呤(6-MP)在体外对L1210细胞的细胞动力学影响方面进行了比较。通过生长速率、细胞体积和细胞周期分布的变化来监测这些动力学扰动。在等摩尔暴露剂量下(基于嘌呤碱的摩尔浓度),0.1 mM聚(s6I)在降低生长速率和细胞总数方面比6-MP更有效。需要将6-MP暴露剂量增加20倍(至2 mM)才能使细胞总数降低至与0.1 mM聚(s6I)相似的水平。对处理后的细胞群体进行库尔特体积分布的同时测定表明,0.1 mM聚(s6I)使平均群体体积的增加幅度大于任何浓度的6-MP。通过流式细胞术获得的细胞周期分布表明,与平均群体体积增加同时,聚(s6I)暴露导致G1期和S期细胞减少,G2期细胞明显积累。用6-MP处理也导致类似的细胞周期重新分布,但程度总是小于聚(s6I)。对这些重新分布的群体进行流式分选表明,在用0.1 mM聚(s6I)处理期间平均群体体积的增加几乎同样归因于G2期细胞百分比的增加和具有G2期DNA含量的细胞体积的增加。然而,对于0.1 mM 6-MP,G2期细胞体积的增加占主导。尽管合成聚(s6I)是为了开发像6-MP这样的生物活性化合物更有效的递送形式,并且它与6-MP具有密切的结构相似性,但其作用机制尚不清楚。

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