Controlled manipulation of TRAIL into single human colon cancer cells using atomic force microscope

Yingmin Qu, Jinyun Liu, Guoliang Wang, Zhengxun Song, Zuobin Wang
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引用次数: 1

Abstract

In this study, an AFM tip was used to penetrate the human colon cancer cells (SW480) in the culture medium containing pEGFP-N1-TRAIL plasmids. The trail plasmids encoded with the enhanced green fluorescent protein (EGFP) were moved into the SW480 cells through membrane holes created by the AFM probe. Following the penetration, the culture medium was changed into the RPMI1640 medium supplemented with 10% of fetal bovine serum and incubated for 24h. The expression of PEGFP-N1-TRAIL in SW480 cells was then observed by inverted fluorescence microscope. The experiment results indicate that the AFM tip can be used to penetrate the membranes of targeted cells individually.
利用原子力显微镜控制TRAIL进入单个人结肠癌细胞
本研究使用AFM尖端在含有pEGFP-N1-TRAIL质粒的培养基中穿透人结肠癌细胞(SW480)。用增强的绿色荧光蛋白(EGFP)编码的trail质粒通过AFM探针形成的膜孔进入SW480细胞。穿透后,将培养基改为添加10%胎牛血清的RPMI1640培养基,孵育24h。倒置荧光显微镜观察PEGFP-N1-TRAIL在SW480细胞中的表达。实验结果表明,AFM尖端可以单独穿透目标细胞的膜。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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