Department of Biomedical Engineering, School of Engineering, Virginia Commonwealth University, Richmond, VA 23284, USA.
Oral Oncol. 2010 Sep;46(9):698-704. doi: 10.1016/j.oraloncology.2010.07.001. Epub 2010 Aug 21.
We designed an epidermal growth factor (EGF)-containing polyamidoamine (PAMAM) Generation 4 dendrimer vector labeled with quantum dots for targeted imaging and nucleic acid delivery. (1)H NMR, SDS-PAGE, and Western blotting were applied to characterize the synthesized G4.0-GGG-EGF nanoparticles. Targeting efficiency, cell viability, proliferation, and intracellular signal transduction were evaluated using HN12, NIH3T3, and NIH3T3/EGFR cells. We found that EGF-conjugated dendrimers did not stimulate growth of EGFR-expressing cells at the selected concentration. Consistent with this, minimal stimulation of post-receptor signaling pathways was observed. These nanoparticles can localize within cells that express the EGFR in a receptor-dependent manner, whereas uptake into cells lacking the receptor was low. A well characterized vimentin shRNA (shVIM) and yellow fluorescent protein (YFP) siRNA were used to test the delivery and transfection efficiency of the constructed targeted vector. Significant knockdown of expression was observed, indicating that this vector is useful for introduction of nucleic acids or drugs into cells by a receptor-targeted mechanism.
我们设计了一种含有表皮生长因子 (EGF) 的聚酰胺-胺 (PAMAM) 四代树状大分子载体,并用量子点进行标记,用于靶向成像和核酸递送。(1)H NMR、SDS-PAGE 和 Western blot 用于表征合成的 G4.0-GGG-EGF 纳米颗粒。使用 HN12、NIH3T3 和 NIH3T3/EGFR 细胞评估靶向效率、细胞活力、增殖和细胞内信号转导。我们发现,在选定的浓度下,EGF 缀合的树突状聚合物不会刺激 EGFR 表达细胞的生长。与此一致,观察到受体后信号通路的最小刺激。这些纳米颗粒可以以受体依赖性方式定位于表达 EGFR 的细胞内,而缺乏受体的细胞摄取则较低。使用经过充分表征的波形蛋白 shRNA (shVIM) 和黄色荧光蛋白 (YFP) siRNA 来测试构建的靶向载体的递送和转染效率。观察到表达的显著敲低,表明该载体可通过受体靶向机制将核酸或药物有效递送至细胞内。