首页> 外文期刊>Biological trace element research >Studies on the mechanism of the selenite-induced decrease in cell attachment: effect of selenite on the levels of fibronectin receptor (alpha5beta1 integrin) mRNAs.
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Studies on the mechanism of the selenite-induced decrease in cell attachment: effect of selenite on the levels of fibronectin receptor (alpha5beta1 integrin) mRNAs.

机译:亚硒酸盐诱导的细胞附着减少的机制研究:亚硒酸盐对纤连蛋白受体(α5beta1整合素)mRNA水平的影响。

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摘要

We previously reported that exposure of HeLa cells to selenite for 2 h results in a decrease in their ability to attach to fibronectin (Yan and Frenkel, Cancer Res. 52, 5803-5807 [1992]), as well as a decrease in the level of fibronectin receptor (alpha5beta1 integrin) at the cell surface (Yan and Frenkel, Biol. Trace Element Res. 46, 79-89 [1994]). We have now found that after exposure to selenite, there was a decrease in the total cellular content of the receptor protein, as well as in the level of the mRNAs for both of the subunits. Exposure of cells to actinomycin D (an inhibitor of RNA synthesis) also resulted in a decrease in the level of these mRNAs, suggesting that the effect of selenite is the result of its known inhibitory effect on RNA synthesis (Frenkel, Toxicol. Lett. 25, 219-223 [1985]). Exposure of cells to actinomycin D for 2 h also resulted in a decrease in the ability of cells to attach to fibronectin. Furthermore, both selenite and actinomycin D caused a decrease in integrin mRNA levels and in cell attachment to fibronectin only when high-density cells were exposed to the agents. In contrast, when low-density cells were exposed,neither agent had any detectable effect on mRNA levels or on cell attachment. These results have suggested the following scheme for the mechanism of the inhibition of cell attachment by selenite: After exposure to selenite for 2 h, there is a significant inhibition of cellular RNA synthesis, which results in a general decrease in the cellular level of those mRNAs with relatively short half-lives, including in particular those of the fibronectin receptor. This leads to a decrease in the intracellular level of the receptor protein and, consequently, in its level at the cell surface, which in turn causes a decrease in the rate of cell attachment to fibronectin.
机译:我们先前曾报道HeLa细胞与亚硒酸盐接触2小时会导致其与纤连蛋白的附着能力降低(Yan和Frenkel,Cancer Res。52,5803-5807 [1992]),并且其水平降低。在细胞表面的纤连蛋白受体(α5β1整联蛋白)的表达(Yan和Frenkel,Biol.Trace Element Res.46,79-89 [1994])。现在我们发现,暴露于亚硒酸盐后,受体蛋白的总细胞含量以及两个亚基的mRNA水平均下降。将细胞暴露于放线菌素D(RNA合成的抑制剂)也导致这些mRNA的水平降低,这表明亚硒酸盐的作用是其对RNA合成的已知抑制作用的结果(Frenkel,Toxicol.Lett。25)。 ,219-223 [1985]。将细胞暴露于放线菌素D 2 h也导致细胞附着于纤连蛋白的能力降低。此外,亚硒酸盐和放线菌素D都仅在高密度细胞暴露于试剂的情况下才导致整联蛋白mRNA水平降低和细胞与纤连蛋白的附着。相比之下,当暴露低密度细胞时,两种药物均未对mRNA水平或细胞附着产生任何可检测的影响。这些结果表明了以下方案对亚硒酸盐抑制细胞附着的机制:暴露于亚硒酸盐2小时后,细胞RNA合成受到显着抑制,这导致这些mRNA的细胞水平普遍下降。具有相对短的半衰期,特别是纤连蛋白受体的半衰期。这导致受体蛋白的细胞内水平降低,因此导致其在细胞表面的水平降低,这进而导致细胞与纤连蛋白的附着速率降低。

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