Ray R M, McCormack S A, Johnson L R
Department of Physiology, College of Medicine, The University of Tennessee Health Science Center, Memphis, Tennessee 38163, USA.
Am J Physiol Gastrointest Liver Physiol. 2001 Jul;281(1):G37-43. doi: 10.1152/ajpgi.2001.281.1.G37.
The polyamines spermidine and spermine and their precursor, putrescine, are required for the growth and proliferation of eukaryotic cells. This study compares and contrasts growth arrest caused by polyamine depletion in the untransformed IEC-6 cell line with that in the p53-mutated colon cancer Caco-2 cell line. Cells were grown in the presence or absence of alpha-difluoromethylornithine (DFMO), a specific inhibitor of ornithine decarboxylase, the first rate-limiting enzyme in the synthesis of polyamines. Depletion of polyamines inhibited the growth of both cell lines equally and over the same time frame. However, whereas IEC-6 cells were arrested in the G(1) phase of the cell cycle, there was no accumulation of Caco-2 cells in any particular phase. In IEC-6 cells, growth arrest was accompanied by elevated levels of p53 and p21(Waf1/Cip1) (p21). There were no changes in p53 levels in Caco-2 cells. Levels of p21 increased in Caco-2 cells on day 2 without any effect on cell cycle progression. The amount of cyclin-dependent kinase (Cdk)2 protein was unchanged by polyamine depletion in both cell lines. However, the activity of Cdk2 was significantly inhibited by DFMO in IEC-6 cells. These data suggest that in the untransformed IEC-6 cells the regulation of Cdk2 activity and progression through the cell cycle are p53- and p21 dependent. Growth arrest in the p53-mutated Caco-2 line after polyamine depletion occurs by a different, yet unknown, mechanism.
多胺亚精胺和精胺及其前体腐胺是真核细胞生长和增殖所必需的。本研究比较并对比了在未转化的IEC - 6细胞系和p53突变的结肠癌细胞Caco - 2细胞系中,多胺耗竭所导致的生长停滞情况。细胞在存在或不存在α - 二氟甲基鸟氨酸(DFMO)的情况下生长,DFMO是鸟氨酸脱羧酶(多胺合成中的第一个限速酶)的特异性抑制剂。多胺的耗竭在相同的时间范围内同等程度地抑制了两种细胞系的生长。然而,IEC - 6细胞停滞在细胞周期的G(1)期,而Caco - 2细胞在任何特定阶段都没有积累。在IEC - 6细胞中,生长停滞伴随着p53和p21(Waf1/Cip1)(p21)水平的升高。Caco - 2细胞中p53水平没有变化。Caco - 2细胞在第2天p21水平升高,但对细胞周期进程没有任何影响。在两种细胞系中,多胺耗竭均未改变细胞周期蛋白依赖性激酶(Cdk)2蛋白的量。然而,在IEC - 6细胞中,DFMO显著抑制了Cdk2的活性。这些数据表明,在未转化的IEC - 6细胞中,Cdk2活性的调节和细胞周期进程是p53和p21依赖性的。多胺耗竭后,p53突变的Caco - 2细胞系中的生长停滞是通过一种不同但未知的机制发生的。