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首页> 外文期刊>Journal of cell biology >Phorbol esters and gene expression: the role of rapid changes in K+ transport in the induction of ornithine decarboxylase by 12-O-tetradecanoylphorbol-13-acetate in BALB/c 3T3 cells and a mutant cell line defective in Na+K+Cl- cotransport.
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Phorbol esters and gene expression: the role of rapid changes in K+ transport in the induction of ornithine decarboxylase by 12-O-tetradecanoylphorbol-13-acetate in BALB/c 3T3 cells and a mutant cell line defective in Na+K+Cl- cotransport.

机译:佛波酯和基因表达:BA- / c 3T3细胞和Na + K + Cl-共转运缺陷型突变细胞系中12-O-十四烷酰phorbol-13-乙酸酯在鸟氨酸脱羧酶诱导中K +转运的快速变化中的作用。

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A BALB/c 3T3 preadipose cell line defective in Na+K+Cl- cotransport (3T3-E12a cells) has been used to study the relationship between phorbol ester-induced rapid changes in cation fluxes and changes in expression of a gene known to be modulated by this agent. In contrast to its effect on parental 3T3 cells, 12-O-tetradecanoylphorbol-13-acetate (TPA) did not inhibit either furosemide-sensitive 86Rb+ influx or the rate of 86Rb+ efflux from preloaded mutant cells. TPA-induced changes in intracellular K+ content were diminished in 3T3-E12a cells as compared with parental cells. Thus, mutation of the Na+K+Cl- cotransport system renders overall potassium transport in mutant cells largely insensitive to modulation by TPA. The morphological and functional responses of 3T3 and 3T3-E12a cells to TPA were also compared. In contrast to the extensive and long-lasting changes in morphology of 3T3 cells after 0.16 microM TPA addition, only slight and shorter-lived morphological effects of TPA were observed in 3T3-E12a cells. The transport properties of mutant cells were not totally unresponsive to TPA since hexose transport (2-deoxyglucose uptake) could be stimulated in both cell types. To establish a possible link between early changes in cation fluxes and activation of gene expression by TPA, the induction of the enzyme ornithine decarboxylase (ODC) was studied in detail. Addition of fresh medium containing serum or exposure to hypoosmotic conditions resulted in the induction of ODC in both 3T3 and 3T3-E12a cells. However, TPA failed to cause an increase in ODC activity in mutant cells, although a substantial induction of the enzyme was seen in parental cells. These results suggest that rapid changes in ion fluxes mediated by the Na+K+Cl- cotransport system are necessary for at least one of the phorbol ester-induced changes in gene expression in responsive cells.
机译:在Na + K + Cl-共转运中存在缺陷的BALB / c 3T3脂肪细胞系(3T3-E12a细胞)已被用于研究佛波酯诱导的阳离子通量快速变化与已知的基因表达变化之间的关系。由该代理调制。与它对亲本3T3细胞的作用相反,12-O-十四烷酰佛波醇13-乙酸盐(TPA)既不抑制速尿敏感的86Rb +流入,也不抑制预载突变细胞的86Rb +外排速率。与亲本细胞相比,TPA诱导的3T3-E12a细胞的细胞内K +含量变化减少。因此,Na + K + Cl-共转运系统的突变使突变细胞中的钾转运总体上对TPA的调节不敏感。还比较了3T3和3T3-E12a细胞对TPA的形态和功能反应。与添加0.16 microM TPA后3T3细胞的形态发生广泛而持久的变化相反,在3T3-E12a细胞中仅观察到TPA的形态和寿命较短​​。由于在两种细胞类型中均可刺激己糖转运(2-脱氧葡萄糖摄取),因此突变细胞的转运特性并非完全不响应TPA。为了建立阳离子通量的早期变化与TPA激活基因表达之间的可能联系,对鸟氨酸脱羧酶(ODC)的诱导进行了详细研究。添加含有血清的新鲜培养基或暴露于低渗条件导致在3T3和3T3-E12a细胞中诱导ODC。然而,尽管在亲代细胞中看到了对该酶的实质性诱导,但是TPA未能引起突变细胞中ODC活性的增加。这些结果表明,至少一种由佛波酯诱导的反应性细胞基因表达变化中,至少需要一种由Na + K + Cl-共转运系统介导的离子通量的快速变化。

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