Shatrova A N, Aksenov N D, Zenin V V
Institute of Cytology RAS, St. Petersburg.
Tsitologiia. 2002;44(11):1068-78.
Studying the effect of topoisomerase II (topo II) inhibitors on cell passage through mitosis seems to be important for understanding the role of this enzyme during chromosome condensation and segregation. A flow cytometric assay (Zenin et al., 2001) allowed to determine the mitotic index, and to discriminate between not only cells in G2 and M phases (including metaphase and anaphase cells), but also cells in pseudo-G1 with 4c DNA content. It is shown that topo II catalytic inhibitor ICRF-193 blocks G2-M transition in a lymphoblastoid cell line GM-130. Addition of caffeine to cells abrogated a block of their entering mitosis but not the inhibitor action. Cells entered mitosis, which was proven by the presence of chromosomes in the examined specimen, and, bypassing anaphase, appeared in pseudo-G1 with 4c DNA content. We have found that in the presence of ICRF-193 cells, GM-130 and Hep-2 lines, previously blocked by nocodazole when in mitosis and then washed, pass through metaphase, enter anaphase and leave it to pass to pseudo-G1 with the 4c DNA content. Thus, by inhibiting topo II activity ICRF-193 causes abnormal mitotic transition.
研究拓扑异构酶II(topo II)抑制剂对细胞有丝分裂进程的影响,对于理解该酶在染色体凝聚和分离过程中的作用似乎至关重要。一种流式细胞术检测方法(Zenin等人,2001年)能够测定有丝分裂指数,不仅可以区分处于G2期和M期的细胞(包括中期和后期细胞),还能区分具有4c DNA含量的假G1期细胞。结果表明,拓扑异构酶II催化抑制剂ICRF - 193在淋巴母细胞系GM - 130中阻断G2 - M期转换。向细胞中添加咖啡因可消除对其进入有丝分裂的阻断,但不能消除抑制剂的作用。细胞进入有丝分裂,这通过检测样本中染色体的存在得以证实,并且绕过后期,出现在具有4c DNA含量的假G1期。我们发现,在存在ICRF - 193的情况下,GM - 130和Hep - 2细胞系在有丝分裂时先前被诺考达唑阻断,随后经洗涤后,会经过中期,进入后期并离开后期进入具有4c DNA含量的假G1期。因此,通过抑制拓扑异构酶II的活性,ICRF - 193会导致异常的有丝分裂转换。