Division of Pharmaceutical Sciences, School of Pharmacy, University of Missouri-Kansas City, Kansas City, MO, USA.
Division of Pharmaceutical Sciences, School of Pharmacy, University of Missouri-Kansas City, Kansas City, MO, USA.
Nanomedicine. 2018 Jan;14(1):51-61. doi: 10.1016/j.nano.2017.08.017. Epub 2017 Sep 7.
Insulin-like growth factor 2 receptor (IGF2R) is overexpressed in activated hepatic stellate cells (HSCs) and therefore can be utilized for HSC-specific drug delivery. We recently discovered an IGF2R-specific peptide using a novel biopanning. Here, we adopted biotin-conjugated IGF2R-specific peptide, cholesterol, and vitamin A as the targeting ligands for the neutravidin-based siRNA nanocomplex to deliver PCBP2 siRNA, a potentially antifibrotic agent, to HSCs. Compared to vitamin A and cholesterol, the IGF2R-specific peptide exhibited the highest targeting effect to human LX-2 HSC, rat HSC-T6 cell line, and activated primary rat HSCs. Accordingly, the IGF2R-specific peptide coupled nanocomplex demonstrated higher silencing activity of PCBP2 and better inhibition on the migration of activated HSCs. Compared to free siRNA and the nanocomplexes coupled with vitamin A and cholesterol, the IGF2R-specific peptide coupled nanocomplex showed the highest uptake in the liver and lowest uptake in the lung and kidney of the rats with CCl-induced liver fibrosis.
胰岛素样生长因子 2 受体(IGF2R)在活化的肝星状细胞(HSCs)中过度表达,因此可用于 HSC 特异性药物传递。我们最近使用一种新的生物淘选技术发现了一种 IGF2R 特异性肽。在这里,我们采用生物素化的 IGF2R 特异性肽、胆固醇和维生素 A 作为基于链霉亲和素的 siRNA 纳米复合物的靶向配体,将潜在的抗纤维化药物 PCBP2 siRNA 递送至 HSCs。与维生素 A 和胆固醇相比,IGF2R 特异性肽对人 LX-2 HSC、大鼠 HSC-T6 细胞系和活化的原代大鼠 HSCs 具有最高的靶向作用。因此,IGF2R 特异性肽偶联纳米复合物表现出更高的 PCBP2 沉默活性,并更好地抑制活化的 HSCs 的迁移。与游离 siRNA 和与维生素 A 和胆固醇偶联的纳米复合物相比,IGF2R 特异性肽偶联的纳米复合物在 CCl 诱导的肝纤维化大鼠的肝脏中具有最高的摄取率,在肺和肾脏中的摄取率最低。