Brink Peter R, Robinson Richard B, Rosen Michael R, Cohen Ira S
Stony Brook University, Department of Physiology and Biophysics, Stony Brook, NY 11794, USA.
IDrugs. 2010 Jun;13(6):383-7.
Current in vivo approaches for the delivery of siRNAs have been hindered by inefficient targeting to cells and by the triggering of immune responses. The cellular delivery of siRNA by immunoprivileged cells avoids the immune response, because the siRNA is delivered from one cell interior to another via gap junctions, thereby avoiding the extracellular compartment. Human mesenchymal stem cells (hMSCs) can be delivered focally or systemically, and have also exhibited the ability to migrate to targeted tissue in vivo. These features suggest the potential use of hMSCs as a cellular delivery system for siRNA. This feature review discusses the role of gap junctions to facilitate the transfer of siRNA directly to target cells, thus avoiding the disadvantages involved with approaches that are dependent on the extracellular space for siRNA delivery.
目前用于递送小干扰RNA(siRNA)的体内方法受到细胞靶向效率低下和免疫反应触发的阻碍。免疫特权细胞对siRNA的细胞递送可避免免疫反应,因为siRNA通过间隙连接从一个细胞内部传递到另一个细胞,从而避开细胞外区室。人间充质干细胞(hMSCs)可以局部或全身递送,并且在体内也表现出迁移到靶组织的能力。这些特性表明hMSCs有可能用作siRNA的细胞递送系统。这篇专题综述讨论了间隙连接在促进siRNA直接转移到靶细胞中的作用,从而避免了依赖细胞外空间进行siRNA递送的方法所具有的缺点。