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[离子稳态变化诱导的某些腹水肿瘤细胞中的核酸合成]

[Nucleic acid synthesis in the cells of some ascites tumors induced by change in ionic homeostasis].

作者信息

Kaz'min S D

出版信息

Biokhimiia. 1981 Jul;46(7):1226-35.

PMID:7272352
Abstract

The DNA and RNA synthesis was studied in the cells of Ehrlich ascite tumour, lymphoma NK/Ly and carcinoma T.O. was studied under conditions when the Na+/K+ ratio was changed by preincubation in salt media at low temperatures. The incorporation of [3H]thymidine was inhibited at a decrease of the Na+/K+ ratio. The high rate of synthesis was observed only when the cells interacted with K+-free media. Under these conditions some cells which had not incorporated the label induced DNA synthesis. RNA synthesis in lymphoma NK/Ly cells was repressed by about 70% at an increase in K+ concentration (cK) up to 30 mM, followed by a further increase and a subsequent decrease at cK greater than 90 mM. In Ehrlich tumour cells the RNA synthesis was increased 2-fold at an increase in cK from 0 to 30 mM and decreased 3-fold within the concentration range of 30-50 mM. At cK of 50-80 mM it remained constant and showed a further decrease at cK greater than 90 mM. As in the case of DNA synthesis this effect was reversible, i. e. when the cells were transferred to a Na+-rich medium the incorporation of the label rapidly increased and reached its maximum after 30-35 min. Ouabain (2 mM) did not prevent the activation. Actinomycin D (0.05 mkg/ml) inhibited the incorporation of [3H]uridine at any values of Na+/K+. Electrophoresis of RNA isolated from the nuclei and cytoplasm of Ehrlich tumour cells showed that the changes in ionic homeostasis result in the synthesis of new forms of RNA. It is concluded that the distribution of Na+ and K+ in intact cell nuclei is uneven and that monovalent cations can control transcription via the tertiary structure of deoxyribonucleoprotein.

摘要

在低温下于盐培养基中预孵育以改变Na⁺/K⁺比值的条件下,研究了艾氏腹水瘤细胞、淋巴瘤NK/Ly细胞和癌T.O.细胞中的DNA和RNA合成。当Na⁺/K⁺比值降低时,[³H]胸腺嘧啶核苷的掺入受到抑制。只有当细胞与无钾培养基相互作用时,才观察到高合成率。在这些条件下,一些未掺入标记物的细胞诱导了DNA合成。当钾离子浓度(cK)增加至30 mM时,淋巴瘤NK/Ly细胞中的RNA合成被抑制约70%,随后在cK大于90 mM时进一步增加并随后下降。在艾氏肿瘤细胞中,当cK从0增加到30 mM时,RNA合成增加2倍,在30 - 50 mM的浓度范围内下降3倍。在cK为50 - 80 mM时保持恒定,在cK大于90 mM时进一步下降。与DNA合成情况一样,这种效应是可逆的,即当细胞转移到富含Na⁺的培养基中时,标记物的掺入迅速增加,并在30 - 35分钟后达到最大值。哇巴因(2 mM)不能阻止这种激活。放线菌素D(0.05 μg/ml)在任何Na⁺/K⁺值下均抑制[³H]尿苷的掺入。对从艾氏肿瘤细胞核和细胞质中分离的RNA进行电泳表明,离子稳态的变化导致了新形式RNA的合成。结论是,完整细胞核中Na⁺和K⁺的分布不均匀,单价阳离子可通过脱氧核糖核蛋白的三级结构控制转录。

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