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电刺激内吞作用在基因电转导中的作用。

The role of electrically stimulated endocytosis in gene electrotransfer.

机构信息

University of Ljubljana, Faculty of Electrical Engineering, Tržaška 25, SI-1000 Ljubljana, Slovenia.

出版信息

Bioelectrochemistry. 2012 Feb;83:38-45. doi: 10.1016/j.bioelechem.2011.08.005. Epub 2011 Aug 23.

Abstract

Gene electrotransfer is an established method for transfer of genes into cells, however, the mechanism of transfer of DNA across the cell membrane is still not known. Some studies suggest that DNA is translocated through membrane pores while others propose that DNA enters the cell via electro-endocytosis, but no direct observation was performed. In this paper we investigated the second hypothesis. Cells were stained with membrane dye FM 1-43FX, which is used for observation of endocytosis, and then exposed to electric pulses. We analyzed if endocytosis was stimulated by applying electric pulses with intensities below and above the threshold value for gene electrotransfer. No increase in endocytosis from 20 min or even up to 2h after the pulse delivery was observed, regardless of the electric field strength. These observations do not correlate with electrotransfer efficiency, which increases with field strength and is observed only above the threshold value. Our results suggest that electro-endocytosis is not a crucial mechanism for gene electrotransfer and that the hypothesis of DNA entry by translocation through permeabilized membrane is more plausible. The presented results are important for better understanding of the mechanisms of gene electrotransfer and for its optimization for clinical applications.

摘要

基因电转移是将基因转入细胞的一种成熟方法,然而,DNA 穿过细胞膜的转移机制仍不清楚。一些研究表明 DNA 通过膜孔移位,而另一些研究则提出 DNA 通过电内吞作用进入细胞,但没有进行直接观察。在本文中,我们研究了第二种假说。用用于观察内吞作用的膜染料 FM 1-43FX 对细胞进行染色,然后施加电脉冲。我们分析了施加低于和高于基因电转移阈值的电脉冲是否会刺激内吞作用。无论电场强度如何,在施加脉冲后 20 分钟甚至 2 小时后,都没有观察到内吞作用的增加。这些观察结果与电转移效率不相关,电转移效率随场强增加,仅在阈值以上观察到。我们的结果表明,电内吞作用不是基因电转移的关键机制,而 DNA 通过穿孔的膜移位进入的假说更合理。这些结果对于更好地理解基因电转移的机制以及优化其用于临床应用非常重要。

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