...
首页> 外文期刊>RSC Advances >Interrogation of drug effects on HeLa cells by exploiting new AFM mechanical biomarkers
【24h】

Interrogation of drug effects on HeLa cells by exploiting new AFM mechanical biomarkers

机译:通过利用新的AFM机械生物标记物询问药物对HeLa细胞的作用

获取原文
           

摘要

New mechanical biomarkers were discovered and used to investigate drug effects on HeLa cells. HeLa cells were measured using advanced atomic force microscopy (AFM) techniques before and after treatment with an anticancer drug (docetaxel, a microtubule polymerizer) and the biomechanical properties of cells were analyzed using theoretical models. The biomechanical results show that the length of the surface brush, the factor of viscosity, and the adhesion work of untreated HeLa cells reduced from 920 nm, 0.72 and 4.12 × 10?16 N m to 673 nm, 0.52 and 5.37 × 10?17 N m for treated cells, respectively. In order to reveal the underlying mechanisms of these changes, transmission electron microscopy (TEM) and western blotting assays were employed to characterize structural changes of the cells. Compared to the untreated cells, TEM images confirmed a thinner brush layer on the surface of treated cells while the western blotting of tubulin extracted from the cells indicated an increased microtubule concentration for the treated cells. These changes are consistent with previous studies on the influence of docetaxel on cells. Based on the above results, we conclude that docetaxel can lead to an increased microtubule network in HeLa cells, a thinner brush layer on HeLa cell surfaces and that the length of surface brush, the factor of viscosity, and the adhesion work can be exploited as effective mechanical biomarkers to evaluate drug effects on HeLa cells. This work demonstrates a new AFM-based technique that can be exploited to assess drug action on cells and is promising for the application of drug screening.
机译:发现了新的机械生物标记,并将其用于研究药物对HeLa细胞的作用。在使用抗癌药(多西他赛,微管聚合器)处理之前和之后,使用先进的原子力显微镜(AFM)技术测量HeLa细胞,并使用理论模型分析细胞的生物力学特性。生物力学结果表明,未处理的HeLa细胞的表面刷长度,粘度因子和粘附功从920 nm,0.72和4.12×10 ?16 N m至673 nm,分别为处理后的细胞的0.52和5.37×10 ?17 N m。为了揭示这些变化的潜在机制,采用透射电子显微镜(TEM)和蛋白质印迹分析来表征细胞的结构变化。与未处理的细胞相比,TEM图像证实处理过的细胞表面刷层更薄,而从细胞中提取的微管蛋白的蛋白质印迹表明处理过的细胞的微管浓度增加。这些变化与以前关于多西紫杉醇对细胞影响的研究一致。根据以上结果,我们得出结论,多西紫杉醇可导致HeLa细胞中微管网络的增加,HeLa细胞表面上较薄的刷子层,并且表面刷子的长度,粘度因子和粘附力可被利用为有效的机械生物标记物,以评估药物对HeLa细胞的作用。这项工作演示了一种新的基于AFM的技术,可用于评估药物对细胞的作用,并有望用于药物筛选。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号