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钙-小干扰 RNA 纳米复合物:逆转性的奥秘。

Calcium-siRNA nanocomplexes: what reversibility is all about.

机构信息

Avram and Stella Goldstein-Goren Department of Biotechnology Engineering, Ben-Gurion University of the Negev, Beer-Sheva 8410501, Israel.

Avram and Stella Goldstein-Goren Department of Biotechnology Engineering, Ben-Gurion University of the Negev, Beer-Sheva 8410501, Israel.

出版信息

J Control Release. 2015 Apr 10;203:150-60. doi: 10.1016/j.jconrel.2015.02.029. Epub 2015 Feb 19.

Abstract

Gene silencing using small interfering RNA (siRNA) relies on the critical need for a safe and effective carrier, capable of strong but reversible complexation, siRNA protection, cellular uptake, and cytoplasmatic unloading of its cargo. We hypothesized that a delivery platform based on the eletrostatic interactions of siRNA with calcium ions in solution would fulfill these needs, ultimately leading to effective gene silencing. Physical characterization of the calcium-siRNA complexes, using high resolution microscopy and dynamic light scattering (DLS), showed the formation of stable nanosized complexes 80nm in diameter, bearing mild (-7mV) negative surface charge. The complexes were extremely stable in the presence of serum proteins or high concentrations of heparin; they maintained their nanosized features in suspension for days; and effectively protected the siRNA from enzymatic degradation. The Ca-siRNA complexes were disintegrated in the presence of Ca-chelating ion exchange resin, thus proving their reversibility. Excellent cytocompatibility of calcium-siRNA complexes was achieved using physiological calcium ion concentrations. The calcium-siRNA complexes successfully induced a very high (~80%) level of gene silencing in several cell types, at both mRNA and protein levels, associated with efficient cellular uptake. Collectively, our results show that the developed delivery platform based on reversible calcium-siRNA interactions offers a simple and versatile method for enhancing the therapeutic efficiency of siRNA.

摘要

利用小干扰 RNA(siRNA)进行基因沉默依赖于安全有效的载体的关键需求,该载体能够进行强烈但可逆的络合、siRNA 保护、细胞摄取以及细胞质中 cargo 的释放。我们假设基于 siRNA 与溶液中钙离子静电相互作用的递药平台将满足这些需求,最终实现有效的基因沉默。使用高分辨率显微镜和动态光散射(DLS)对钙-siRNA 复合物进行物理特性分析,表明形成了稳定的纳米尺寸复合物,直径约为 80nm,并带有轻微的(约-7mV)负表面电荷。这些复合物在存在血清蛋白或高浓度肝素的情况下极其稳定;它们在悬浮液中保持纳米尺寸特征数天;并有效地保护 siRNA 免受酶降解。在存在钙螯合离子交换树脂的情况下,Ca-siRNA 复合物会解体,从而证明其具有可逆性。使用生理钙离子浓度,实现了钙-siRNA 复合物的优异细胞相容性。钙-siRNA 复合物在几种细胞类型中成功诱导了非常高(约 80%)的基因沉默水平,在 mRNA 和蛋白质水平上都有,同时伴随着有效的细胞摄取。总之,我们的研究结果表明,基于可逆钙-siRNA 相互作用的开发的递药平台为提高 siRNA 的治疗效率提供了一种简单而通用的方法。

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