Hall Arnaldur, Lächelt Ulrich, Bartek Jiri, Wagner Ernst, Moghimi Seyed Moein
Genome Integrity Unit, Danish Cancer Society Research Center, 2100 Copenhagen, Denmark.
Pharmaceutical Biotechnology, Department of Pharmacy, Ludwig-Maximilians-Universität, 81377 Munich, Germany; Nanosystems Initiative Munich, 80799 Munich, Germany.
Mol Ther. 2017 Jul 5;25(7):1476-1490. doi: 10.1016/j.ymthe.2017.01.024. Epub 2017 Mar 6.
Polyethylenimine (PEI) is a gold standard polycationic transfectant. However, the highly efficient transfecting activity of PEI and many of its derivatives is accompanied by serious cytotoxic complications and safety concerns at innate immune levels, which impedes the development of therapeutic polycationic nucleic acid carriers in general and their clinical applications. In recent years, the dilemma between transfection efficacy and adverse PEI activities has been addressed from in-depth investigations of cellular processes during transfection and elucidation of molecular mechanisms of PEI-mediated toxicity and translation of these integrated events to chemical engineering of novel PEI derivatives with an improved benefit-to-risk ratio. This review addresses these perspectives and discusses molecular events pertaining to dynamic and multifaceted PEI-mediated cytotoxicity, including membrane destabilization, mitochondrial dysfunction, and perturbations of glycolytic flux and redox homeostasis as well as chemical strategies for the generation of better tolerated polycations. We further examine the effect of PEI and its derivatives on complement activation and interaction with Toll-like receptors. These perspectives are intended to lay the foundation for an improved understanding of interlinked mechanisms controlling transfection and toxicity and their translation for improved engineering of polycation-based transfectants.
聚乙烯亚胺(PEI)是一种金标准聚阳离子转染剂。然而,PEI及其许多衍生物的高效转染活性伴随着严重的细胞毒性并发症以及在先天免疫水平上的安全性问题,这总体上阻碍了治疗性聚阳离子核酸载体的发展及其临床应用。近年来,通过对转染过程中细胞过程的深入研究、阐明PEI介导的毒性分子机制以及将这些综合事件转化为具有改善的风险效益比的新型PEI衍生物的化学工程,解决了转染效率与PEI不良活性之间的困境。本综述阐述了这些观点,并讨论了与动态和多方面的PEI介导的细胞毒性相关的分子事件,包括膜不稳定、线粒体功能障碍、糖酵解通量和氧化还原稳态的扰动以及生成耐受性更好的聚阳离子的化学策略。我们进一步研究了PEI及其衍生物对补体激活的影响以及与Toll样受体的相互作用。这些观点旨在为更好地理解控制转染和毒性的相互关联机制及其转化以改进基于聚阳离子的转染剂工程奠定基础。