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Cationic cholesterol-dependent LNP delivery to lung stem cells, the liver, and heart.

Afsane RadmandHyejin KimJared BeyersdorfCurtis N DobrowolskiRyan ZenhausernKalina PaunovskaSebastian G HuayamaresXuanwen HuaKeyi HanDavid LoughreyMarine Z C HatitAda Del CidHuanzhen NiAram ShajiiAndrea LiAbinaya MuralidharanHannah E PeckKaren E TiegreenShu JiaPhilip J SantangeloJames E Dahlman
Published in: Proceedings of the National Academy of Sciences of the United States of America (2024)
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.
Keyphrases
  • stem cells
  • regulatory t cells
  • fatty acid
  • cell therapy
  • single cell
  • heart failure
  • immune response
  • mesenchymal stem cells
  • deep learning