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Regulation of integrin αV subunit expression by sulfatide in hepatocellular carcinoma cells

机译:硫化物对肝癌细胞中整合素αV亚单位表达的调控

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摘要

Integrin is important in migration and metastasis of tumor cells. Changes of integrin expression and distribution will cause an alteration of cellular adhesion and migration behaviors. In this study, we investigated sulfatide regulation of the integrin αV subunit expression in hepatoma cells and observed that either exogenous or endogenous sulfatide elicited a robust upregulation of integrin αV subunit mRNA and protein expression in hepatoma cells. This regulatory effect occurred with a corresponding phosphorylation (T739) of the transcription factor Sp1. Based on the electrophoretic mobility shift assay, sulfatide enhanced the integrin αV promoter activity and strengthened the Sp1 complex super-shift. The results of chromatin immunoprecipitation analysis also indicated that sulfatide enhanced Sp1 binding to the integrin αV promoter in vivo. Silence of Sp1 diminished the stimulation of integrin αV expression by sulfatide. In the early stage of sulfatide stimulation, phosphorylation of Erk as well as c-Src was noted, and inhibition of Erk activation with either U0126 or PD98059 significantly suppressed Sp1 phosphorylation and integrin αV expression. We demonstrated that sulfatide regulated integrin αV expression and cell adhesion, which was associated with Erk activation.
机译:整联蛋白在肿瘤细胞的迁移和转移中很重要。整联蛋白表达和分布的变化将引起细胞粘附和迁移行为的改变。在这项研究中,我们调查了肝细胞中整合素αV亚基表达的硫酸盐调节,并观察到外源或内源性硫化物均会引起肝癌细胞中整合素αV亚基mRNA和蛋白质表达的强烈上调。这种调节作用是通过转录因子Sp1的相应磷酸化(T739)发生的。基于电泳迁移率变动分析,硫酸盐增强了整联蛋白αV启动子的活性并增强了Sp1复合物的超转变。染色质免疫沉淀分析的结果还表明,硫化物在体内增强了Sp1与整联蛋白αV启动子的结合。 Sp1的沉默减少了硫化物对整联蛋白αV表达的刺激。在硫化物刺激的早期阶段,注意到Erk以及c-Src的磷酸化,并且用U0126或PD98059抑制Erk活化可显着抑制Sp1磷酸化和整联蛋白αV表达。我们证明了硫酸脂调节整联蛋白αV表达和细胞粘附,这与Erk激活有关。

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