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首页> 外文期刊>BioMetals: An International Journal on the Role of Metal Ions in Biology, Biochemistry and Medicine >Effects of cadmium on the sub-cellular localization of β-catenin and β-catenin-regulated gene expression in NRK-52E cells
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Effects of cadmium on the sub-cellular localization of β-catenin and β-catenin-regulated gene expression in NRK-52E cells

机译:镉对NRK-52E细胞β-catenin亚细胞定位及β-catenin调节基因表达的影响

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The E-cadherin/β-catenin complex is a structural component of adherens-type junctions in epithelial cells. Moreover, β-catenin acts as an intracellular signaling molecule that can influence the expression of a variety of genes that regulate apoptosis and cell cycle control. Cadmium (Cd) is an environmental toxicant that causes renal dysfunction and disrupts cadherin-dependent cell-cell adhesion in various types of epithelial cells. In this study, we examined the effects of Cd on the subcellular localization of β-catenin, the cadherin/β-catenin complex and β-catenin-mediated gene transcription in rat proximal tubule NRK-52E cells. Exposure to 5-10 lM Cd for 4 h caused the NRK cells to separate from each other without killing the cells or causing them to detach from the growing surface. This effect was associated with the loss of β-catenin and E-cadherin from the cell-cell contacts and apparent changes in the accumulation of β-catenin in the nuclear cell subfraction. The expression of the β-catenin-sensitive gene, c-jun was significantly increased in cells exposed to 5 lM Cd. However, there was no change in the expression of several other β-catenin-regulated genes including: c-myc, cyclin D1 and matrilysin. Additional studies utilizing the TOPFLASH β-catenin reporter gene construct showed that Cd caused a 2-3 fold increase in the expression of the luciferase reporter gene. Overall, these results indicate that Cd disrupts the cadherin/β-catenin complex in NRK-52E cells, but this effect leads to only partial activation of β-catenin- mediated gene transcription.
机译:E-钙粘蛋白/β-连环蛋白复合物是上皮细胞中粘附型连接的结构成分。此外,β-catenin充当细胞内信号分子,可以影响调节细胞凋亡和细胞周期控制的各种基因的表达。镉(Cd)是一种环境毒物,可导致肾功能不全并破坏各种类型的上皮细胞中依赖钙粘着蛋白的细胞粘附。在这项研究中,我们研究了镉对大鼠近端肾小管NRK-52E细胞中β-catenin,钙粘蛋白/β-catenin复合物和β-catenin介导的基因转录亚细胞定位的影响。暴露于5-10 lM Cd中4小时会导致NRK细胞彼此分离,而不会杀死细胞或使它们从生长表面脱离。这种作用与细胞间接触中β-catenin和E-cadherin的损失以及核细胞亚组分中β-catenin积聚的明显变化有关。在暴露于5 lM Cd的细胞中,β-catenin敏感基因c-jun的表达明显增加。但是,其他几个受β-连环蛋白调节的基因的表达没有变化,包括:c-myc,cyclin D1和基质溶素。利用TOPFLASHβ-catenin报告基因构建物的其他研究表明,Cd导致萤光素酶报告基因表达增加了2-3倍。总体而言,这些结果表明Cd破坏了NRK-52E细胞中的钙粘蛋白/β-连环蛋白复合物,但是这种作用仅导致β-连环蛋白介导的基因转录的部分活化。

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