Multifunctional Magnetic Nanocarriers for Image-Tagged SiRNA Delivery to Intact Pancreatic Islets

被引:26
作者
Medarova, Zdravka [1 ]
Kumar, Mohanraja [1 ]
Ng, Shu-wing [2 ]
Yang, Junzheng [2 ]
Barteneva, Natasha [3 ,4 ]
Evgenov, Natalia V. [1 ]
Petkova, Victoria [5 ]
Moore, Anna [1 ]
机构
[1] Harvard Univ, Massachusetts Gen Hosp, Sch Med,Mol Imaging Lab, MGH MIT HMS,Athinoula A Martinos Ctr Biomed Imagi, Charlestown, MA 02129 USA
[2] Brigham & Womens Hosp, Dept Obstet Gynecol & Reprod Biol, Div Gynecol Oncol, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Immune Dis Inst, Boston, MA USA
[4] Harvard Univ, Sch Med, Dept Pathol, Boston, MA 02115 USA
[5] Harvard Univ, Beth Israel Deaconess Med Ctr, Sch Med, Boston, MA 02215 USA
关键词
Magnetic resonance imaging; Optical imaging; RNA interference; Pancreatic islets;
D O I
10.1097/TP.0b013e31818a81b2
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. With the ultimate hope of finding a cure for diabetes, researches are looking into altering the genetic profile of the beta cell as a way to manage metabolic dysregulation. One of the most powerful new approaches for the directed regulation of gene expression uses the phenomenon of RNA interference. Methods. Here, we establish the feasibility of a novel technology centered around multifunctional magnetic nanocarriers, which concurrently deliver siRNA to intact pancreatic islets and can be detected by magnetic resonance and optical imaging. Results. In the proof-of-principle studies described here, we demonstrate that, after in vitro incubation, magnetic nanoparticles carrying siRNA designed to target the model gene for enhanced green fluorescent protein are efficiently taken up by murine pancreatic islets, derived from egfp transgenic animals. This uptake can be visualized by magnetic resonance imaging and near-infrared fluorescence optical imaging and results in suppression of the target gene. Conclusions. These results illustrate the value of our approach in overcoming the challenges associated with genetic modification of intact pancreatic islets in a clinically acceptable manner. Furthermore, an added advantage of our technology derives from the combined capability of our magnetic nanoparticles for siRNA delivery and magnetic labeling of pancreatic islets.
引用
收藏
页码:1170 / 1177
页数:8
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