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[CHO-K1细胞及该细胞系对溴化乙锭耐药的克隆细胞中蛋白激酶C活性的差异]

[Differences in the protein kinase C activity in CHO-K1 cells and in clone cells of this line resistant to ethidium bromide].

作者信息

Nekrasova T P

出版信息

Tsitologiia. 1993;35(8):38-46.

PMID:8266573
Abstract

Protein kinase C (PK C) activity in cells of two ethidium bromide (EB) resistant clones with different proliferating rates, derived from CHO-K1 cell line, was assayed. After selection in the presence of 1 mkg/ml EB cells of isolated clones acquired cross-resistance also to some unrelated drugs of different structure. It is shown that resistant cells after the first step of selection elevated PK C activity level in membrane fractions. Subsequent increase in resistance (from 1 to 10 mkg/ml EB) led to a further elevated enzyme activity both in cytosolic and membrane fractions in cells of both variants. The effect of EB presence in cultural media on the enzyme activity was tested. EB at a subtoxic concentration was shown to cause an increased PK C activity both in cytosolic and membrane fractions from resistant cells sublines.

摘要

对源自CHO-K1细胞系的两个增殖速率不同的溴化乙锭(EB)抗性克隆细胞中的蛋白激酶C(PKC)活性进行了测定。在1μg/ml EB存在下进行筛选后,分离克隆的细胞对一些结构不同的无关药物也获得了交叉抗性。结果表明,在第一步筛选后的抗性细胞中,膜组分中的PKC活性水平升高。随后抗性增加(从1μg/ml EB增加到10μg/ml EB)导致两个变体细胞的胞质和膜组分中的酶活性进一步升高。测试了培养基中EB的存在对酶活性的影响。结果显示,亚毒性浓度的EB会导致抗性细胞亚系的胞质和膜组分中的PKC活性增加。

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