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纳米载体介导的靶向干细胞分化的 siRNA 递呈

Nanocarrier Mediated siRNA Delivery Targeting Stem Cell Differentiation.

机构信息

Department of Biological Sciences, BITS Pilani, K. K. Birla Goa campus, Zuarinagar, Goa-403726, India.

出版信息

Curr Stem Cell Res Ther. 2020;15(2):155-172. doi: 10.2174/1574888X14666191202095041.

Abstract

Stem cell-based regenerative medicine holds exceptional therapeutic potential and hence the development of efficient techniques to enhance control over the rate of differentiation has been the focus of active research. One of the strategies to achieve this involves delivering siRNA into stem cells and exploiting the RNA interference (RNAi) mechanism. Transport of siRNA across the cell membrane is a challenge due to its anionic property, especially in primary human cells and stem cells. Moreover, naked siRNA incites immune responses, may cause off-target effects, exhibits low stability and is easily degraded by endonucleases in the bloodstream. Although siRNA delivery using viral vectors and electroporation has been used in stem cells, these methods demonstrate low transfection efficiency, cytotoxicity, immunogenicity, events of integration and may involve laborious customization. With the advent of nanotechnology, nanocarriers which act as novel gene delivery vehicles designed to overcome the problems associated with safety and practicality are being developed. The various nanomaterials that are currently being explored and discussed in this review include liposomes, carbon nanotubes, quantum dots, protein and peptide nanocarriers, magnetic nanoparticles, polymeric nanoparticles, etc. These nanodelivery agents exhibit advantages such as low immunogenic response, biocompatibility, design flexibility allowing for surface modification and functionalization, and control over the surface topography for achieving the desired rate of siRNA delivery and improved gene knockdown efficiency. This review also includes discussion on siRNA co-delivery with imaging agents, plasmid DNA, drugs etc. to achieve combined diagnostic and enhanced therapeutic functionality, both for in vitro and in vivo applications.

摘要

基于干细胞的再生医学具有特殊的治疗潜力,因此,开发有效的技术来增强对分化速度的控制一直是研究的重点。实现这一目标的策略之一是将 siRNA 递送到干细胞中,并利用 RNA 干扰 (RNAi) 机制。由于其阴离子特性,siRNA 穿过细胞膜的运输是一个挑战,尤其是在原代人细胞和干细胞中。此外,裸露的 siRNA 会引发免疫反应,可能导致脱靶效应,表现出低稳定性,并容易被血液中的核酸酶降解。尽管使用病毒载体和电穿孔将 siRNA 递送至干细胞中已有报道,但这些方法的转染效率低、细胞毒性、免疫原性、整合事件较高,并且可能涉及繁琐的定制。随着纳米技术的出现,正在开发纳米载体作为新型基因传递载体,旨在克服与安全性和实用性相关的问题。目前正在探索和讨论的各种纳米材料包括脂质体、碳纳米管、量子点、蛋白质和肽纳米载体、磁性纳米颗粒、聚合物纳米颗粒等。这些纳米递药系统具有低免疫原性、生物相容性、设计灵活性,允许表面修饰和功能化,以及控制表面形貌以实现所需的 siRNA 递药速度和提高基因敲低效率等优点。本综述还讨论了 siRNA 与成像剂、质粒 DNA、药物等的共递药,以实现体外和体内应用的联合诊断和增强治疗功能。

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