Svensson Robert U, Shey Michael R, Ballas Zuhair K, Dorkin J Robert, Goldberg Michael, Akinc Akin, Langer Robert, Anderson Daniel G, Bumcrot David, Henry Michael D
Department of Molecular Physiology and Biophysics and Pathology, Roy J. and Lucille A. Carver College of Medicine, University of Iowa, Iowa City, Iowa 52240, USA.
Mol Ther. 2008 Dec;16(12):1995-2001. doi: 10.1038/mt.2008.187. Epub 2008 Sep 9.
A significant barrier to the successful general development of small-interfering RNA (siRNA) therapeutics is the ability to deliver them systemically to target organs and cell types. In this study, we have developed a mouse strain that will facilitate the evaluation of the efficacy of siRNA delivery strategies. This strain contains robust ubiquitous expression of firefly luciferase from germ line Cre-mediated recombination of the ROSA26-LSL-Luc allele. We show that luciferase is highly and uniformly expressed in all tissues examined. Using this mouse model, we describe a facile assay that enables the assessment of the pharmacodynamics of a systemically delivered siRNA formulation. These mice can also be used as universal donors, enabling the efficient and sensitive monitoring of cell trafficking or tissue transplantation. The primary advantage of this approach is that siRNA efficacy against a nonessential target can be easily evaluated in any tissue. This strain should generally enhance the ability to rapidly screen, compare and optimize various siRNA formulations for tissue-targeted or -enhanced systemic delivery in a preclinical development setting.
小干扰RNA(siRNA)疗法成功广泛发展的一个重大障碍是将其全身递送至靶器官和细胞类型的能力。在本研究中,我们培育出了一种小鼠品系,它将有助于评估siRNA递送策略的疗效。该品系通过种系中Cre介导的ROSA26-LSL-Luc等位基因重组,实现萤火虫荧光素酶的强大且普遍的表达。我们发现荧光素酶在所检测的所有组织中均高度且均匀地表达。利用这个小鼠模型,我们描述了一种简便的检测方法,可用于评估全身递送的siRNA制剂的药效学。这些小鼠还可作为通用供体,实现对细胞转运或组织移植的高效且灵敏的监测。这种方法的主要优势在于,针对非必需靶点的siRNA疗效能够在任何组织中轻松评估。该品系通常应能增强在临床前研发环境中快速筛选、比较和优化各种用于组织靶向或增强全身递送的siRNA制剂的能力。