The State Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Nanjing University, Nanjing, 210023, China,
Changzhou High-Tech Research Institute of Nanjing University and Jiangsu Target Pharma Laboratories Inc., Changzhou, China,
Int J Nanomedicine. 2018 Oct 24;13:6603-6623. doi: 10.2147/IJN.S176991. eCollection 2018.
The discovery and development of RNA interference has made a tremendous contribution to the biochemical and biomedical field. However, liposomal transfection protocols to deliver siRNAs to certain types of cells, eg, immune cells, are not viable due to exceedingly low transfection efficiency. While viral delivery and electroporation are two widely adopted approaches to transfect immune cells, they are associated with certain drawbacks such as complexity of preparation, biosafety issues, and high cytotoxicity. We believe amendments can be made to liposomal formulas and protocols to achieve a highly efficient knockdown of genes by liposome-loaded siRNAs.
The aim of this study was to use the apoptotic-mimic Ca-PS lipopolyplex to achieve highly efficient siRNA knockdown of genes in the hard-to-transfect macrophages with reduced cytotoxicity and more efficient cellular uptake.
We devised an anionic liposomal formula containing phosphatidylserine to mimic the apoptotic body, the Ca-PS lipopolyplex. Ca-PS lipopolyplex was proven to be capable of delivering and effecting efficient gene knockdown in multiple cell lines at lowered cytotoxicity. Among the two types of macrophages, namely Ana-1 and bone-marrow derived macrophages, Ca-PS lipopolyplex showed an improvement in knockdown efficiency, as high as 157%, over Lipo2000. Further investigations revealed that Ca-PS promotes increased cellular uptake, lysosomal escape and localization of siRNAs to the perinuclear regions in macrophages. Lastly, transfection by Ca-PS lipopolyplex did not induce spontaneous polarization of macrophages.
The apoptotic body-mimic Ca-PS lipopolyplex is a stable, non-cytotoxic liposomal delivery system for siRNAs featuring vastly improved potency for macrophages and lowered cytotoxicity. It is speculated that Ca-PS lipopolyplex can be applied to other immune cells such as T cells and DC cells, but further research efforts are required to explore its promising potentials.
RNA 干扰的发现和发展为生化和生物医学领域做出了巨大贡献。然而,由于转染效率极低,将 siRNA 递送至某些类型的细胞(例如免疫细胞)的脂质体转染方案不可行。虽然病毒传递和电穿孔是转染免疫细胞的两种广泛采用的方法,但它们存在一些缺点,例如制备复杂、生物安全问题和高细胞毒性。我们相信可以对脂质体配方和方案进行修改,以通过负载 siRNA 的脂质体实现基因的高效敲低。
本研究旨在使用凋亡模拟 Ca-PS 脂质体聚合物实现难以转染的巨噬细胞中基因的高效 siRNA 敲低,同时降低细胞毒性和提高细胞摄取效率。
我们设计了一种含有磷脂酰丝氨酸的阴离子脂质体配方来模拟凋亡小体,即 Ca-PS 脂质体聚合物。Ca-PS 脂质体聚合物已被证明能够在降低细胞毒性的情况下在多种细胞系中递送和实现有效的基因敲低。在两种巨噬细胞(即 Ana-1 和骨髓来源的巨噬细胞)中,Ca-PS 脂质体聚合物的敲低效率比 Lipo2000 提高了 157%。进一步的研究表明,Ca-PS 促进了巨噬细胞中 siRNA 的细胞摄取、溶酶体逃逸和向核周区域的定位增加。最后,Ca-PS 转染不会诱导巨噬细胞自发极化。
凋亡小体模拟 Ca-PS 脂质体聚合物是一种稳定、非细胞毒性的 siRNA 递送系统,对巨噬细胞具有极高的效力,同时降低了细胞毒性。推测 Ca-PS 脂质体聚合物可以应用于其他免疫细胞,如 T 细胞和 DC 细胞,但需要进一步的研究努力来探索其潜在的应用。