Institute of Technology, University of Tartu, 1 Nooruse Street, 50411 Tartu, Estonia.
Biochim Biophys Acta Gen Subj. 2024 Dec;1868(12):130719. doi: 10.1016/j.bbagen.2024.130719. Epub 2024 Oct 5.
The successful delivery of therapeutic nucleic acids (NAs) into eukaryotic cells is essential for numerous biomedical applications, including gene therapy, gene silencing, and genome editing. Cell-penetrating peptides (CPPs) have claimed significant attention as delivery vehicles due to their inherent ability to penetrate cellular membranes and efficiently transport cargo, including NAs, into the cells. However, further optimization and a deeper understanding of underlying mechanisms are necessary for such transfection methods. Previous studies have demonstrated that Ca ions can significantly enhance NA delivery efficiency when included in transfection media or CPP/NA nanoparticles during preparation. Similar effects have been observed for Mg, but the impact of other ions in this context has not been thoroughly investigated. In this study, we supplemented the CPP/NA formulations with various inorganic biocompatible ions by introducing solutions of the respective salts to colloidal nanoparticles at the preparation stage. Our results indicated that supplementing the CPP/NA formulations with certain salt solutions enhanced the biological effect achieved with NAs while also influencing nanoparticle size, surface charge, complexation stability, and, to some extent, the internalization route. Our findings offer valuable insights for optimizing the formation of CPP nanoparticles to improve NA delivery efficiency.
将治疗性核酸(NAs)递送到真核细胞中对于许多生物医学应用至关重要,包括基因治疗、基因沉默和基因组编辑。细胞穿透肽(CPPs)由于其内在的穿透细胞膜的能力以及将包括 NAs 在内的货物有效递送到细胞内的能力,引起了人们的极大关注。然而,对于这种转染方法,需要进一步优化和更深入地了解其潜在机制。先前的研究表明,在转染培养基或 CPP/NA 纳米颗粒的制备过程中包含 Ca 离子可以显著提高 NA 的递送效率。在这种情况下,Mg 也有类似的影响,但尚未彻底研究其他离子的影响。在这项研究中,我们通过在制备阶段将相应盐的溶液引入胶体纳米颗粒中,用各种无机生物相容性离子补充 CPP/NA 制剂。我们的结果表明,用某些盐溶液补充 CPP/NA 制剂可以增强 NAs 达到的生物学效果,同时还影响纳米颗粒大小、表面电荷、络合稳定性,并且在某种程度上影响内化途径。我们的发现为优化 CPP 纳米颗粒的形成以提高 NA 递送效率提供了有价值的见解。