前中期染色体技术的比较——以秋碱的作用为重点。

In Vitro Pub Date : 1984-12-01 DOI:10.1007/BF02619667
J E Wiley, L M Sargent, S L Inhorn, L F Meisner
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引用次数: 4

摘要

评估了六种不同的技术,以更好地定义那些对获得前期中期细胞进行条带分析最关键的技术因素。我们的研究结果表明:暴露于半胱氨酸30分钟或更短的时间对增加前中期细胞的产量没有影响,暴露于超过0.1微克/毫升的半胱氨酸可能是有毒的,甲氨蝶呤显著降低有丝分裂指数,似乎只是因为它抑制了后期形式而增加了前中期细胞的发生率;(d)低浓度放线菌素d(0.5微克/毫升)和秋碱(0.1微克/毫升)联合暴露4小时,可以获得细胞遗传学上满意的最优数量的前期细胞。该技术抑制染色体凝聚,同时允许前期中期细胞积累4小时。
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Comparison of prometaphase chromosome techniques with emphasis on the role of colcemid.

Six different techniques were evaluated to define better those technical factors that are most critical for obtaining prometaphase cells for banding analysis. Our results demonstrate: colcemid exposures of 30 min or less have no effect on increasing the yield of prometaphase cells, colcemid exposures of greater than 0.1 microgram/ml can be toxic, methotrexate depresses the mitotic index significantly and seems to increase the incidence of prometaphase cells only because it suppresses later forms; and (d) the optimum number of cytogenetically satisfactory prometaphase cells can be obtained with a 4-h exposure to a combination of low concentration actinomycin D (0.5 microgram/ml) and colcemid (0.1 microgram/ml). This technique inhibits chromosome condensation while permitting prometaphase cells to accumulate for 4 h.

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