Ghosh S, Paweletz N
Eur J Cell Biol. 1984 Nov;35(2):304-11.
Multinucleate (MN) cells were induced in PtK1 cells by colcemid treatment. A large percentage of cells developed nuclear asynchrony both in relation to DNA synthesis and mitosis within one cell cycle. Asynchrony could be traced even in metaphase and anaphase cells in which interphase nuclei, PCC of S-phase nuclei and less condensed prophase-like chromosomes could be observed along with normally condensed chromosomes. The occurrence of such abnormalities in these large MN cells may be explained on the basis of an uneven distribution of inducer molecules of DNA synthesis and mitosis due to cytoplasmic compartmentation. The less condensed form of all the chromosomes except chromosome 4 could be traced in asynchronous metaphase. The failure of the less condensed chromosomes to undergo complete condensation does not always appear to result from late entry of nuclei containing these chromosomes into G2 phase. It is likely that chromosome 4 carries gene(s) for chromosome condensation, as this chromosome itself never appears in a less condensed form. The inducers for chromosome condensation may not always be available at equal concentrations to all chromosomes located in separate nuclei, thus they may sometimes fail to undergo complete condensation before other nuclei reach the end of prophase, when the nuclear envelopes of all nuclei present in the cell break down simultaneously.
通过秋水仙酰胺处理在PtK1细胞中诱导产生多核(MN)细胞。在一个细胞周期内,很大比例的细胞在DNA合成和有丝分裂方面出现核不同步。即使在中期和后期细胞中也能追踪到不同步现象,在这些细胞中,除了正常浓缩的染色体外,还能观察到间期核、S期核的早熟凝集染色体以及不太浓缩的前期样染色体。这些大型MN细胞中出现此类异常现象,可能是由于细胞质分隔导致DNA合成和有丝分裂诱导分子分布不均所致。在异步中期,除了4号染色体外,所有染色体不太浓缩的形态都能被追踪到。不太浓缩的染色体未能完全浓缩,似乎并不总是因为含有这些染色体的核进入G2期较晚。4号染色体可能携带染色体浓缩相关基因,因为这条染色体自身从未以不太浓缩的形态出现。染色体浓缩诱导因子对于位于不同细胞核中的所有染色体而言,其浓度可能并不总是相等,因此在其他细胞核到达前期末期(此时细胞中所有细胞核的核膜同时解体)之前,它们有时可能无法完全浓缩。