Trayford Chloe, Wilhalm Alissa, Habibovic Pamela, Smeets Hubert, van Tienen Florence, van Rijt Sabine
Department of Instructive Biomaterials Engineering, MERLN Institute for Technology-Inspired Regenerative Medicine, Maastricht University, P.O. Box 616, 6200 MD, Maastricht, The Netherlands.
Department of Toxicogenomics, School for Mental Health and Neuroscience, Maastricht University, PO Box 616, 6200 MD, Maastricht, The Netherlands.
Discov Nano. 2023 Dec 21;18(1):161. doi: 10.1186/s11671-023-03926-1.
Mutations in nuclear and mitochondrial genes are responsible for severe chronic disorders such as mitochondrial myopathies. Gene therapy using antisense oligonucleotides is a promising strategy to treat mitochondrial DNA (mtDNA) diseases by blocking the replication of the mutated mtDNA. However, transport vehicles are needed for intracellular, mitochondria-specific transport of oligonucleotides. Nanoparticle (NP) based vectors such as large pore mesoporous silica nanoparticles (LP) often rely on surface complexation of oligonucleotides exposing them to nucleases and limiting mitochondria targeting and controlled release ability. In this work, stable, fluorescent, hollow silica nanoparticles (HSN) that encapsulate and protect oligonucleotides in the hollow core were synthesized by a facile one-pot procedure. Both rhodamine B isothiocyanate and bis[3-(triethoxysilyl)propyl]tetrasulfide were incorporated in the HSN matrix by co-condensation to enable cell tracing, intracellular-specific degradation and controlled oligonucleotide release. We also synthesized LP as a benchmark to compare the oligonucleotide loading and release efficacy of our HSN. Mitochondria targeting was enabled by NP functionalization with cationic, lipophilic Triphenylphosphine (TPP) and, for the first time a fusogenic liposome based carrier, previously reported under the name MITO-Porter. HSN exhibited high oligonucleotide incorporation ratios and release dependent on intracellular degradation. Further, MITO-Porter capping of our NP enabled delayed, glutathione (GSH) responsive oligonucleotide release and mitochondria targeting at the same efficiency as TPP functionalized NP. Overall, our NP are promising vectors for anti-gene therapy of mtDNA disease as well as many other monogenic disorders worldwide.
核基因和线粒体基因的突变是导致线粒体肌病等严重慢性疾病的原因。使用反义寡核苷酸的基因疗法是一种有前景的治疗线粒体DNA(mtDNA)疾病的策略,通过阻断突变mtDNA的复制来实现。然而,寡核苷酸的细胞内、线粒体特异性运输需要运输载体。基于纳米颗粒(NP)的载体,如大孔介孔二氧化硅纳米颗粒(LP),通常依赖于寡核苷酸的表面络合,这会使它们暴露于核酸酶,并限制线粒体靶向和控释能力。在这项工作中,通过简便的一锅法合成了稳定、荧光、中空二氧化硅纳米颗粒(HSN),其在中空核心中封装并保护寡核苷酸。异硫氰酸罗丹明B和双[3-(三乙氧基硅基)丙基]四硫化物通过共缩合被掺入HSN基质中,以实现细胞追踪、细胞内特异性降解和寡核苷酸的控释。我们还合成了LP作为基准,以比较我们的HSN的寡核苷酸负载和释放效果。通过用阳离子、亲脂性三苯基膦(TPP)对NP进行功能化,以及首次使用一种基于融合脂质体的载体(以前称为MITO-Porter)来实现线粒体靶向。HSN表现出高寡核苷酸掺入率和依赖于细胞内降解的释放。此外,我们的NP的MITO-Porter封端能够实现延迟的、谷胱甘肽(GSH)响应的寡核苷酸释放,并以与TPP功能化NP相同的效率实现线粒体靶向。总体而言,我们的NP是用于mtDNA疾病以及全球许多其他单基因疾病的抗基因治疗的有前景的载体。