Laboratory of Molecular Neurobiology, Neurobiology Center, Nencki Institute of Experimental Biology of the Polish Academy of Sciences, Warsaw, 02-093, Poland.
Aix-Marseille Université, CNRS, Center Interdisciplinaire de Nanoscience de Marseille, UMR 7325, Equipe Labellisée Ligue Contre le Cancer, 13288, Marseille, France.
Nanomedicine (Lond). 2019 Sep;14(18):2441-2458. doi: 10.2217/nnm-2019-0176. Epub 2019 Aug 28.
Alterations of microglia, the brain-resident macrophages, are associated with numerous brain pathologies. Genetic manipulation of microglia in diseases using small interfering RNA (siRNA) is hampered by the lack of safe and efficient siRNA delivery methods. We assessed the amphiphilic dendrimer (AD) for functional siRNA delivery and gene knockdown in primary microglia. We characterized the ability of AD to form nanoparticles with siRNA, and studied their size, surface potential, cell uptake and gene silencing in rodent microglia. AD effectively delivered siRNA to primary microglia and decreased target gene and protein expression, leading to transcriptomic changes without affecting basal microglial functions. The dendrimer AD promises to be an innocuous carrier for siRNA delivery into microglia.
小胶质细胞是大脑中固有的巨噬细胞,其改变与许多脑部疾病有关。使用小干扰 RNA (siRNA) 对疾病中小胶质细胞进行基因操作受到缺乏安全有效的 siRNA 传递方法的阻碍。我们评估了两亲性树突(AD)在原代小胶质细胞中功能性 siRNA 传递和基因敲低的作用。我们描述了 AD 与 siRNA 形成纳米颗粒的能力,并研究了它们在啮齿动物小胶质细胞中的大小、表面电位、细胞摄取和基因沉默。AD 能有效地将 siRNA 递送至原代小胶质细胞,降低靶基因和蛋白的表达,导致转录组发生变化,而不影响小胶质细胞的基础功能。树突状聚合物 AD 有望成为一种安全的 siRNA 传递载体,用于小胶质细胞的基因治疗。