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9,10-蒽二酮-1,4-双[[2-[(2-羟乙基)氨基]乙基]氨基]二乙酸酯对弗瑞德白血病细胞的细胞形态和核酸的影响

Effects of 9,10-anthracenedione, 1,4-bis[[2-[(2-hydroxyethyl)amino]-ethyl]amino]-, diacetate on cell morphology and nucleic acids of friend leukemia cells.

作者信息

Evenson D P, Traganos F, Darzynkiewicz Z, Staiano-Coico L, Melamed M R

出版信息

J Natl Cancer Inst. 1980 Apr;64(4):857-66.

PMID:6928997
Abstract

Treatment of Friend leukemia cells for 18 hours with 9,10-anthracenedione, 1,4-bis[[(2-hydroxyethyl)amino]ethyl]amino]-, diacetate (ANT) at concentrations up to 1.0 microgram/ml induced significant changes in cell metabolism and structure. Alterations in cell nucleic acid content were detected in cells stained with acridine orange under conditions such that DNA and RNA contents could be measured simultaneously by flow cytometry. Cells treated for 18 hours with ANT at concentrations of 0.05-0.1 microgram/ml became partially blocked at the G2 phase. In addition, about 30% of the cells became polyploid and demonstrated diplochromosomes at the 8C level of mitosis. The nuclear chromatin of blocked cells had an altered structure as reflected by a change in sensitivity of DNA in situ to denaturation induced by low pH. All viable cells treated with ANT for 18 hours at concentrations of 0.4-1.0 microgram/ml were blocked in G2 phase. These cells had significantly more RNA than did untreated cells. Transmission electron microscopic observations of thin-sectioned cells suggested that this increased RNA content in ANT-treated cells was mostly due to an approximately 50% increased cell diameter and partly due to a disproportionate increase in nucleolar size. In addition, electron microscopy revealed that ANT caused increased chromatin condensation and granulation. The drug had no apparent effect on production of the endogenous Friend murine leukemia virus.

摘要

用浓度高达1.0微克/毫升的9,10 - 蒽二酮 - 1,4 - 双[[(2 - 羟乙基)氨基]乙基]氨基] - 二乙酸酯(ANT)处理弗瑞德白血病细胞18小时,可诱导细胞代谢和结构发生显著变化。在用吖啶橙染色的细胞中检测到细胞核酸含量的改变,在此条件下可通过流式细胞术同时测量DNA和RNA含量。用浓度为0.05 - 0.1微克/毫升的ANT处理18小时的细胞在G2期出现部分阻滞。此外,约30%的细胞变成多倍体,并在有丝分裂的8C水平显示出双染色体。阻滞细胞的核染色质结构发生改变,这可通过低pH诱导的原位DNA变性敏感性变化反映出来。用浓度为0.4 - 1.0微克/毫升的ANT处理18小时的所有活细胞都被阻滞在G2期。这些细胞的RNA含量明显高于未处理的细胞。对超薄切片细胞的透射电子显微镜观察表明,ANT处理细胞中RNA含量的增加主要是由于细胞直径增加了约50%,部分是由于核仁大小不成比例地增加。此外,电子显微镜显示ANT导致染色质凝聚和颗粒化增加。该药物对内源性弗瑞德鼠白血病病毒的产生没有明显影响。

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