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α-辅肌动蛋白4和钠氢交换子调节因子1在微电场刺激人宫颈癌Hela细胞迁移中的作用机制
Mechanistic study on the effect of α-actinin 4 and NHERF1 induced migration of human cervical cancer cells treated by EF
【摘要】 目的探讨α-actinin 4和NHERF1在微电场刺激人宫颈癌Hela细胞迁移运动中的分子机制。方法试验分为阴性对照组(control)、加电组(EF)、NHERF1基因沉默组(siRNA)、基因沉默加电组(siRNA+EF)。(1)RT-qPCR检测各组细胞NHERF1和α-actinin 4 mRNA的表达。(2)划痕试验观察各组细胞迁移速度。结果 (1)与对照组比较,EF组NHERF1的表达明显增加;siRNA组和siRNA+EF组NHERF1的表达均明显降低。siRNA+EF组NHERF1的表达比siRNA组稍有增加。EF组α-actinin 4的表达明显减少;siRNA组α-actinin 4的表达明显增加;siRNA+EF组α-actinin 4的表达增加,但差异无显著性。(2)与对照组比较,EF组细胞迁移速度明显增加;siRNA组细胞迁移速度明显降低;siRNA+EF组细胞迁移速度高于siRNA组。结论 NHERF1调节α-actinin 4的表达,在微电场刺激人宫颈癌Hela细胞迁移运动中起作用。
【Abstract】 Objective To investigate the mechanism of α-actinin 4 and NHERF1 induced migration of human cervical cancer cells treated by EF. Methods The grouping experiment was divided into control group,EF group,NHERF1 siRNA group,and siRNA + EF group.(1)The expression of NHERF1 and α-actinin 4 mrna was detected by RT-qPCR.(2)The cell migration rate was measured by scratch test. Results(1)Compared with the control group,the expression of NHERF1 mRNA increased significantly in EF group,and decreased in siRNA group and siRNA+EF group;the expression of NHERF1 mRNA in siRNA+EF group is slightly higher than that of siRNA group. The expression of α-actinin 4 mRNA decreased significantly in EF group,and increased in siRNA group;the expression of α-actinin 4 mRNA in siRNA+EF group is higher,but there was no significant difference.(2)Compared with the control group,the cell migration rate of EF group increased significantly in EF group;the migration rate of cells decreased significantly in siRNA group;the cell migration rate of siRNA + EF group was higher than that of siRNA group. Conclusion NHERF1 regulates the expression of α-actinin 4,which plays a role in the migration of HeLa cells stimulated by EF.
【Key words】 α-actinin 4; NHERF1; Human cervical cancer cells; Cell migraton; Direct current electric fields;
- 【文献出处】 实用医药杂志 ,Practical Journal of Medicine & Pharmacy , 编辑部邮箱 ,2021年03期
- 【分类号】R737.33
- 【被引频次】1
- 【下载频次】51