Petit Institute for Bioengineering and Biosciences, Georgia Institute of Technology, Atlanta, GA 30332.
Department of Chemical Engineering, Georgia Institute of Technology, Atlanta, GA 30332.
Proc Natl Acad Sci U S A. 2024 Mar 12;121(11):e2307801120. doi: 10.1073/pnas.2307801120. Epub 2024 Mar 4.
Adding a cationic helper lipid to a lipid nanoparticle (LNP) can increase lung delivery and decrease liver delivery. However, it remains unclear whether charge-dependent tropism is universal or, alternatively, whether it depends on the component that is charged. Here, we report evidence that cationic cholesterol-dependent tropism can differ from cationic helper lipid-dependent tropism. By testing how 196 LNPs delivered mRNA to 22 cell types, we found that charged cholesterols led to a different lung:liver delivery ratio than charged helper lipids. We also found that combining cationic cholesterol with a cationic helper lipid led to mRNA delivery in the heart as well as several lung cell types, including stem cell-like populations. These data highlight the utility of exploring charge-dependent LNP tropism.
向脂质纳米颗粒(LNP)中添加阳离子辅助脂质可以增加肺部传递并减少肝脏传递。然而,目前尚不清楚电荷依赖性趋向性是普遍存在的,还是取决于带电荷的成分。在这里,我们报告的证据表明,阳离子胆固醇依赖性趋向性可能与阳离子辅助脂质依赖性趋向性不同。通过测试 196 个 LNPs 将 mRNA 递送到 22 种细胞类型的情况,我们发现带电荷的胆固醇导致的肺部:肝脏传递比例与带电荷的辅助脂质不同。我们还发现,将阳离子胆固醇与阳离子辅助脂质结合使用会导致 mRNA 在心脏以及几种肺细胞类型(包括干细胞样群体)中传递。这些数据突出了探索电荷依赖性 LNP 趋向性的实用性。