a Immunology Research Center, Tabriz University of Medical Sciences , Tabriz , Iran.
b Student Research Committee, Tabriz University of Medical Sciences , Tabriz , Iran.
Artif Cells Nanomed Biotechnol. 2016 Nov;44(7):1589-96. doi: 10.3109/21691401.2015.1102738. Epub 2015 Oct 26.
RNA interference (RNAi) guided by small interfering RNAs (siRNA), because of its potential to target and silence the expression of specific genes is utilized as an effective tool in a variety of biological applications. RNAi guided by siRNAs is a powerful tool to attain gene silencing in mammalian cells. One of the features which make siRNA as an amazing biological tool is extremely specific knockdown of target genes by degradation of analogous mRNAs. However, various non-specific effects limit the use of RNAi including the activation of innate immunity and inhibition of inadvertent target genes. One of the most common non-specific effects is inducing the innate immune system including cytoplasmic and endosomal activation of innate immune system, potentially offending the single in mammals. This activation is mainly interceded by immune cells, regularly through a Toll-like receptor (TLR) pathway. The siRNA sequence association of these pathways changes with the sort and position of the TLR involved. In contrast, non-immune cell activation can also arise generally siRNAs which enter into cytoplasm interacting with cytoplasmic RNA sensors such as retinoic acid-inducible gene I. Here, we explain the off-target effects of siRNAs that activate innate immune system and methods to alleviate them, to help enable impressive application of this exciting technology, Also we bold the aspect of molecular strategies permitting the design of therapeutic siRNAs with minute off-target effects.
RNA 干扰 (RNAi) 由小干扰 RNA (siRNA) 指导,由于其能够靶向和沉默特定基因的表达,因此被用作各种生物应用中的有效工具。siRNA 指导的 RNAi 是在哺乳动物细胞中实现基因沉默的有力工具。使 siRNA 成为一种惊人的生物工具的特点之一是通过降解类似的 mRNAs 极其特异性地敲低靶基因。然而,各种非特异性效应限制了 RNAi 的使用,包括先天免疫的激活和对意外靶基因的抑制。最常见的非特异性效应之一是诱导先天免疫系统,包括细胞质和内体先天免疫系统的激活,这可能会对哺乳动物造成单一的威胁。这种激活主要由免疫细胞介导,通常通过 Toll 样受体 (TLR) 途径。这些途径与 TLR 相关的 siRNA 序列关联会随着所涉及的 TLR 类型和位置而变化。相比之下,非免疫细胞的激活也可以由一般进入细胞质的 siRNA 引起,这些 siRNA 与细胞质 RNA 传感器相互作用,如视黄酸诱导基因 I。在这里,我们解释了激活先天免疫系统的 siRNA 的脱靶效应及其减轻方法,以帮助实现这项令人兴奋的技术的显著应用。我们还突出了允许设计具有微小脱靶效应的治疗性 siRNA 的分子策略的方面。