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哪种热方法(加热 DNA 或细胞)能提高哺乳动物细胞中的基因表达?

Which one of the thermal approaches (heating DNA or cells) enhances the gene expression in mammalian cells?

机构信息

Department of Cellular and Molecular Biology, Faculty of Advanced Sciences and Technology, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran.

Department of Hepatitis and AIDS, Pasteur Institute of Iran, Tehran, Iran.

出版信息

Biotechnol Lett. 2021 Oct;43(10):1955-1966. doi: 10.1007/s10529-021-03176-0. Epub 2021 Sep 5.

Abstract

OBJECTIVES

Heat treatment as a physical method could increase the cellular uptake of nucleic acids. In this study, the effects of heat shock were evaluated to enhance the transfection efficiency of three plasmid DNAs into HeLa and TC-1 cancerous, and HEK-293 T and Vero non-cancerous cell lines using lipofectamine 2000 reagent.

METHODS

Two methods of cell- and DNA-based heat treatment were used. Heating DNA solution was performed at 94 °C for 5, 10 and 15 min, and also 72 °C for 30, 60 and 120 min, individually. Moreover, heating the cells was done by incubation at 42 °C for 2 h in different times such as before, during and after DNA transfection.

RESULTS

Our data showed that the conformation of plasmid DNAs was changed at different temperatures with increasing time. The heat-treated plasmid DNAs (94 °C for 10 min or 72 °C for 30 min) indicated higher transfection efficiency than untreated plasmid DNAs (p < 0.05). Furthermore, heat treatment of cells before and during the transfection was higher than untreated cells (p < 0.01). Our results demonstrated that DNA transfection efficiency in cancerous cells was less than non-cancerous cells (p < 0.01).

CONCLUSION

Generally, these findings showed that transfection mediated by thermal stimulation could enhance gene transfection in mammalian cell lines.

摘要

目的

热处理作为一种物理方法,可以增加细胞对核酸的摄取。本研究评估了热休克对三种质粒 DNA 转染 HeLa 和 TC-1 癌细胞系以及 HEK-293T 和 Vero 非癌细胞系的转染效率的影响,使用了脂质体 2000 试剂。

方法

采用细胞和基于 DNA 的两种热处理方法。加热 DNA 溶液分别在 94°C 下加热 5、10 和 15 分钟,以及在 72°C 下加热 30、60 和 120 分钟。此外,通过在不同时间(转染前、转染中和转染后)将细胞孵育在 42°C 2 小时来加热细胞。

结果

我们的数据表明,质粒 DNA 的构象在不同温度下随时间的增加而发生变化。与未经处理的质粒 DNA(p<0.05)相比,经热处理(94°C 10 分钟或 72°C 30 分钟)的质粒 DNA 显示出更高的转染效率。此外,转染前和转染期间对细胞进行热处理比未经处理的细胞更高(p<0.01)。我们的结果表明,癌细胞中的 DNA 转染效率低于非癌细胞(p<0.01)。

结论

一般来说,这些发现表明热刺激介导的转染可以增强哺乳动物细胞系中的基因转染。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1be5/8418791/f452e6725fff/10529_2021_3176_Fig1_HTML.jpg

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