p53-independent apoptosis and p53-dependent block of DNA rereplication following mitotic spindle inhibition in human cells

被引:93
|
作者
Casenghi, M
Mangiacasale, R
Tuynder, M
Caillet-Fauquet, P
Elhajouji, A
Lavia, P
Mousset, S
Kirsch-Volders, M
Cundari, E
机构
[1] Univ La Sapienza, CNR, Ctr Genet Evoluz, I-00185 Rome, Italy
[2] Free Univ Brussels, Lab Biophys & Radiobiol, B-1640 Rhode St Genese, Belgium
[3] Free Univ Brussels, Biol Cellulaire Lab, B-1050 Brussels, Belgium
关键词
mitotic spindle inhibitors; checkpoint; polyploidy; p53; apoptosis; cell cycle;
D O I
10.1006/excr.1999.4554
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We have studied the response of human transformed cells to mitotic spindle inhibition. Two paired cell lines, K562 and its parvovirus-resistant KS derivative clone, respectively nonexpressing and expressing p53, were continuously exposed to nocodazole. Apoptotic cells were observed in both lines, indicating that mitotic spindle impairment induced p53-independent apoptosis, After a transient mitotic delay, both cell lines exited mitosis, as revealed by flow-cytometric determination of MPM2 antigen and cyclin B1 expression, coupled to cytogenetic analysis of sister centromere separation. Both cell lines exited mitosis without chromatid segregation. K562 p53-deficient cells further resumed DNA synthesis, giving rise to cells with a DNA content above 4C, and reentered a polyploid cycle. In contrast, KS cells underwent a subsequent G1 arrest in the tetraploid state. Thus, G1 arrest in tetraploid cells requires p53 function in the rereplication check-point which prevents the G1/S transition following aberrant mitosis; in contrast, p53 expression is dispensable for triggering the apoptotic response in the absence of mitotic spindle. (C) 1999 Academic Press.
引用
收藏
页码:339 / 350
页数:12
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