Technical Chemistry I and Center for Nanointegration Duisburg-Essen (CENIDE), University of Duisburg-Essen, Universitaetsstr. 7, 45141 Essen, Germany.
Institute of Medical Microbiology, University Hospital Essen, University Duisburg-Essen, Hufelandstr. 55, 45147 Essen, Germany.
Sci Rep. 2016 Jul 6;6:28709. doi: 10.1038/srep28709.
Immune responses have to be tightly controlled to guarantee maintenance of immunological tolerance and efficient clearance of pathogens and tumorigenic cells without induction of unspecific side effects. CD4(+) CD25(+) regulatory T cells (Tregs) play an important role in these processes due to their immunosuppressive function. Genetic modification of Tregs would be helpful to understand which molecules and pathways are involved in their function, but currently available methods are limited by time, costs or efficacy. Here, we made use of biofunctionalized gold nanoparticles as non-viral carriers to transport genetic information into murine Tregs. Confocal microscopy and transmission electron microscopy revealed an efficient uptake of the bioconjugates by Tregs. Most importantly, coupling eGFP-siRNA to those particles resulted in a dose and time dependent reduction of up to 50% of eGFP expression in Tregs isolated from Foxp3eGFP reporter mice. Thus, gold particles represent a suitable carrier for efficient import of nucleic acids into murine CD4(+) CD25(+) Tregs, superior to electroporation.
免疫应答必须受到严格控制,以保证在不引起非特异性副作用的情况下维持免疫耐受和有效清除病原体和肿瘤细胞。CD4(+) CD25(+)调节性 T 细胞(Tregs)因其免疫抑制功能在这些过程中发挥重要作用。对 Tregs 进行基因修饰有助于了解其功能涉及哪些分子和途径,但目前可用的方法受到时间、成本或疗效的限制。在这里,我们利用生物功能化的金纳米粒子作为非病毒载体将遗传信息导入到小鼠 Tregs 中。共聚焦显微镜和透射电子显微镜显示 Tregs 能够有效地摄取生物缀合物。最重要的是,将 eGFP-siRNA 与这些颗粒偶联,导致从 Foxp3eGFP 报告小鼠中分离的 Tregs 中 eGFP 表达减少了 50%,这与剂量和时间呈依赖性。因此,金纳米粒子是一种将核酸有效导入小鼠 CD4(+) CD25(+) Tregs 的合适载体,优于电穿孔。