Department of Clinical Sciences Lund, Oncology, Faculty of Medicine, Lund University, Lund, Sweden.
Wang-Cai Biochemistry Lab, Division of Natural and Applied Sciences, Duke Kunshan University, Kunshan, Jiangsu, China.
Nat Commun. 2023 Feb 25;14(1):1075. doi: 10.1038/s41467-023-36752-1.
Endosomal escape and subsequent cytosolic delivery of small interfering RNA (siRNA) therapeutics is believed to be highly inefficient. Since it has not been possible to quantify cytosolic amounts of delivered siRNA at therapeutic doses, determining delivery bottlenecks and total efficiency has been difficult. Here, we present a confocal microscopy-based method to quantify cytosolic delivery of fluorescently labeled siRNA during lipid-mediated delivery. This method enables detection and quantification of sub-nanomolar cytosolic siRNA release amounts from individual release events with measures of quantitation confidence for each event. Single-cell kinetics of siRNA-mediated knockdown in cells expressing destabilized eGFP unveiled a dose-response relationship with respect to knockdown induction, depth and duration in the range from several hundred to thousands of cytosolic siRNA molecules. Accurate quantification of cytosolic siRNA, and the establishment of the intracellular dose-response relationships, will aid the development and characterization of novel delivery strategies for nucleic acid therapeutics.
内体逃逸和随后的小干扰 RNA(siRNA)治疗药物的细胞质递送被认为效率非常低。由于不可能在治疗剂量下定量细胞质中递送的 siRNA 量,因此确定递送瓶颈和总效率一直很困难。在这里,我们提出了一种基于共聚焦显微镜的方法,用于定量脂质介导递送过程中荧光标记 siRNA 的细胞质递送。该方法能够检测和定量来自单个释放事件的亚纳摩尔级细胞质 siRNA 释放量,并对每个事件进行定量置信度的测量。在表达不稳定 eGFP 的细胞中,siRNA 介导的基因沉默的单细胞动力学揭示了与诱导、深度和持续时间有关的剂量反应关系,其范围从几百到几千个细胞质 siRNA 分子。准确定量细胞质中的 siRNA,并建立细胞内的剂量反应关系,将有助于核酸治疗药物新型递送策略的开发和表征。