不同细胞周期阶段人外周血淋巴细胞的磷酸酶抑制剂与染色体过早凝聚。

R Kanda, K Eguchi-Kasai, I Hayata
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引用次数: 37

摘要

观察了人外周血淋巴细胞对冈田酸和calyculin A的细胞遗传学反应。Calyculin A诱导PCC的效果是冈田酸的20倍。从它们的剂量依赖性和染色体形态判断它们诱导PCC的机制相似。与早期研究表明化学物质不能在细胞周期蛋白B较少的G1细胞中诱导PCC相反,本研究表明,calyculin A不仅可以在S和G2/M阶段诱导淋巴细胞PCC,而且在体外PHA刺激后的第二G1期也可以诱导PCC。即使calyculin A浓度增加100倍,淋巴细胞在G0期和体外第一G1期均有轻微的PCC诱导。发现钙离子载体A23187增加了calyculin A诱导的G0-PCC的频率,尽管需要进一步细化以获得适合细胞遗传学研究的G0-PCC形态。
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Phosphatase inhibitors and premature chromosome condensation in human peripheral lymphocytes at different cell-cycle phases.

The cytogenetical reaction of human peripheral lymphocytes to okadaic acid and calyculin A was examined. Calyculin A could induce PCC about 20 times more effectively than okadaic acid. Their mechanisms of PCC induction were judged similar by their dose-dependent manner and chromosome morphology. Contrary to earlier studies suggesting that chemicals could not induce PCC in G1 cells where little cyclin B is present, the present study showed that calyculin A could induce PCC in lymphocytes not only at S and G2/M but also at the second G1 phase after PHA stimulation in vitro. PCC was induced slightly in lymphocytes both at G0 and the first in vitro G1 phase even when the calyculin A concentration increased one hundred fold. It was found that calcium ionophore A23187 increased frequencies of G0-PCC induced by calyculin A, although a further refinement is necessary to obtain a suitable morphology of G0-PCC for cytogenetic studies.

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