RNA Therapeutics Institute, University of Massachusetts Medical School, Worcester, MA, USA.
Department of Molecular Medicine, University of Massachusetts Medical School, Worcester, MA, USA.
Nucleic Acids Res. 2019 Feb 20;47(3):1070-1081. doi: 10.1093/nar/gky1232.
Efficient delivery of therapeutic RNA beyond the liver is the fundamental obstacle preventing its clinical utility. Lipid conjugation increases plasma half-life and enhances tissue accumulation and cellular uptake of small interfering RNAs (siRNAs). However, the mechanism relating lipid hydrophobicity, structure, and siRNA pharmacokinetics is unclear. Here, using a diverse panel of biologically occurring lipids, we show that lipid conjugation directly modulates siRNA hydrophobicity. When administered in vivo, highly hydrophobic lipid-siRNAs preferentially and spontaneously associate with circulating low-density lipoprotein (LDL), while less lipophilic lipid-siRNAs bind to high-density lipoprotein (HDL). Lipid-siRNAs are targeted to lipoprotein receptor-enriched tissues, eliciting significant mRNA silencing in liver (65%), adrenal gland (37%), ovary (35%), and kidney (78%). Interestingly, siRNA internalization may not be completely driven by lipoprotein endocytosis, but the extent of siRNA phosphorothioate modifications may also be a factor. Although biomimetic lipoprotein nanoparticles have been explored for the enhancement of siRNA delivery, our findings suggest that hydrophobic modifications can be leveraged to incorporate therapeutic siRNA into endogenous lipid transport pathways without the requirement for synthetic formulation.
有效的将治疗性 RNA 递送至肝脏以外的部位是阻止其临床应用的根本障碍。脂质偶联可增加 RNA 的血浆半衰期,并增强小干扰 RNA(siRNA)在组织中的积累和细胞摄取。然而,脂质疏水性、结构和 siRNA 药代动力学之间的关系的机制尚不清楚。在这里,我们使用多种天然存在的脂质,表明脂质偶联直接调节 siRNA 的疏水性。当体内给药时,疏水性较强的脂质-siRNA 优先并自发地与循环中的低密度脂蛋白(LDL)结合,而疏水性较弱的脂质-siRNA 则与高密度脂蛋白(HDL)结合。脂质-siRNA 被靶向到富含脂蛋白受体的组织,在肝脏(65%)、肾上腺(37%)、卵巢(35%)和肾脏(78%)中引发显著的 mRNA 沉默。有趣的是,siRNA 的内化可能不完全由脂蛋白内吞作用驱动,但是 siRNA 硫代磷酸酯修饰的程度也可能是一个因素。尽管仿生脂蛋白纳米颗粒已被探索用于增强 siRNA 的递送,但我们的研究结果表明,疏水性修饰可被利用将治疗性 siRNA 整合到内源性脂质运输途径中,而无需合成制剂。