Department of Pharmaceutical Sciences, College of Pharmacy, Robertson Life Sciences Building, Oregon State University, Portland, Oregon 97201, USA.
Department of Pharmaceutical Sciences, College of Pharmacy, Robertson Life Sciences Building, Oregon State University, Portland, Oregon 97201, USA and Department of Biomedical Engineering, Robertson Life Sciences Building, Oregon Health & Science University, Portland, Oregon 97201, USA.
Biomater Sci. 2021 Jun 15;9(12):4289-4300. doi: 10.1039/d0bm01947j.
Lipid-based nanoparticles (LNPs) for the delivery of mRNA have jumped to the forefront of non-viral gene delivery. Despite this exciting development, poor endosomal escape after LNP cell entry remains an unsolved, rate-limiting bottleneck. Here we report the use of a galectin 8-GFP (Gal8-GFP) cell reporter system to visualize the endosomal escape capabilities of LNP-encapsulated mRNA. LNPs substituted with phytosterols in place of cholesterol exhibited various levels of Gal8 recruitment in the Gal8-GFP reporter system. In live-cell imaging, LNPs containing β-sitosterol (LNP-Sito) showed a 10-fold increase in detectable endosomal perturbation events when compared to the standard cholesterol LNPs (LNP-Chol), suggesting the superior capability of LNP-Sito to escape from endosomal entrapment. Trafficking studies of these LNPs showed strong localization with late endosomes. This highly sensitive and robust Gal8-GFP reporter system can be a valuable tool to elucidate intricacies of LNP trafficking and ephemeral endosomal escape events, enabling advancements in gene delivery.
基于脂质的纳米颗粒(LNPs)已成为 mRNA 传递的首选非病毒基因传递载体。尽管这一发展令人兴奋,但 LNP 进入细胞后的内体逃逸仍然是一个未解决的、限速的瓶颈。在这里,我们报告了使用半乳糖凝集素 8-GFP(Gal8-GFP)细胞报告系统来可视化 LNP 包裹的 mRNA 的内体逃逸能力。用植物固醇替代胆固醇的 LNPs 在 Gal8-GFP 报告系统中表现出不同程度的 Gal8 募集。在活细胞成像中,与标准胆固醇 LNPs(LNP-Chol)相比,含有 β-谷甾醇的 LNP(LNP-Sito)显示出可检测到的内体扰动事件增加了 10 倍,这表明 LNP-Sito 具有更好的从内体捕获中逃逸的能力。这些 LNPs 的运输研究显示与晚期内体的强烈定位。这种高度敏感和强大的 Gal8-GFP 报告系统可以成为阐明 LNP 运输和短暂内体逃逸事件复杂性的有价值工具,从而推动基因传递的发展。