Light-induced gene expression using messenger RNA molecules.

Sigurd Bøe, Stein Saebøe-Larssen, Eivind Hovig
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引用次数: 15

Abstract

The exploration of messenger RNA (mRNA) as a potential therapeutic regulator of gene expression has been significantly reduced by the inability of polyplexes to escape the endocytic pathway, combined with the lack of specific targeting. In the present study, we have developed a site-specific delivery strategy for mRNA molecules through the use of photochemical internalization (PCI) technology. When using EGFP mRNA as a model system, a 10- to 40-fold increase in EGFP-positive cells was obtainable in PCI-treated samples, compared to untreated PCI samples in a human osteosarcoma cell line. The amount of EGFP-positive cells in both PCI and non PCI-treated samples were highly dependent on the nitrogen/phosphate (N/P) ratio. Potent delivery of mRNA molecules through the endocytic pathway by the use of polyplexes and PCI was achievable without any loss of cell viability. The main benefit of the strategy proposed is the possibility for protein production from the delivered mRNA in a way that is controllable in a time- and site-specific manner.

利用信使RNA分子进行光诱导基因表达。
信使RNA (mRNA)作为基因表达的潜在治疗调节因子的探索,由于多聚体无法逃脱内吞途径,加上缺乏特异性靶向,已经大大减少了。在目前的研究中,我们通过使用光化学内化(PCI)技术开发了mRNA分子的位点特异性递送策略。当使用EGFP mRNA作为模型系统时,与未经PCI处理的人骨肉瘤细胞系样品相比,PCI处理的样品中EGFP阳性细胞增加了10至40倍。在PCI和非PCI处理的样品中,egfp阳性细胞的数量高度依赖于氮/磷酸盐(N/P)比率。在不损失细胞活力的情况下,利用多聚体和PCI通过内吞途径有效地递送mRNA分子是可以实现的。所提出的策略的主要好处是可能以一种可控的方式从递送的mRNA中产生蛋白质,这种方式具有时间和位点特异性。
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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来源期刊
Oligonucleotides
Oligonucleotides 生物-生化与分子生物学
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