Cell-targeted gene modification by delivery of CRISPR-Cas9 ribonucleoprotein complexes in pseudotyped lentivirus-derived nanoparticles
To fully utilize the potential of CRISPR-Cas9-mediated genome editing, time-restricted and targeted delivery is crucial. By modulating the pseudotype of engineered lentivirus-derived nanoparticles (LVNPs), we demonstrate efficient cell-targeted delivery of Cas9/single guide RNA (sgRNA) ribonucleoprotein (RNP) complexes, supporting gene modification in a defined subset of cells in mixed cell populations. LVNPs pseudotyped with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein resulted in angiotensin-converting enzyme 2 (ACE2)-dependent insertion or deletion (indel) formation in an ACE2<sup>+</sup>/ACE2<sup>-</sup> population of cells, whereas Nipah virus glycoprotein pseudotyping resulted in Ephrin-B2/B3-specific gene knockout. Additionally, LVNPs pseudotyped with Edmonston strain measles virus glycoproteins (MV-H/F) delivered Cas9/sgRNA RNPs to CD46<sup>+</sup> cells with and without additional expression of SLAM (signaling lymphocytic activation molecule; CD150). However, an engineered SLAM-specific measles virus pseudotype (measles virus-hemagglutinin/fusion [MV-H/F]-SLAM) efficiently targeted LVNPs to SLAM<sup>+</sup> cells. Lentiviral vectors (LVs) pseudotyped with MV-H/F-SLAM efficiently transduced >80% of interleukin (IL)-4/IL-21-stimulated primary B cells cultured on CD40 ligand (CD40L)-expressing feeder cells. Notably, LVNPs pseudotyped with MV-H/F and MV-H/F-SLAM reached indel rates of >80% and >60% in stimulated primary B cells, respectively. Collectively, our findings demonstrate the modularity of LVNP-directed delivery of ready-to-function Cas9/sgRNA complexes. Using a panel of different pseudotypes, we provide evidence that LVNPs can be engineered to induce effective indel formation in a subpopulation of cells defined by the expression of surface receptors.
Authors
- Jagesh V. Shah (ORCID: https://orcid.org/0009-0001-1427-6177)
- Albert Ruzo
- Charlotte Møller
- Anne Bruun Rovsing (ORCID: https://orcid.org/0000-0002-0510-180X)
- Ian Helstrup Nielsen (ORCID: https://orcid.org/0009-0003-8736-9838)
- Andreas Bøggild (ORCID: https://orcid.org/0000-0003-2130-3521)
- Thomas Boesen (ORCID: https://orcid.org/0000-0002-5633-6844)
- Emil Aagaard Thomsen (ORCID: https://orcid.org/0000-0002-2685-7745)
- Søren E. Degn (ORCID: https://orcid.org/0000-0001-5409-045X)
- Jacob Giehm Mikkelsen (ORCID: https://orcid.org/0000-0002-1322-3209)
- Jacob Hørlück Janns
- Frederikke Nedergaard
Institutions
- Aarhus University (DK)
- Sana Biotechnology (United States) (US)
Publication Details
- Journal
- Molecular Therapy — Nucleic Acids
- Published
- 2024-08-30
- DOI
- https://doi.org/10.1016/j.omtn.2024.102318
- Citations
- 10
- Primary Topic
- CRISPR and Genetic Engineering
- Type
- article
- Field-Weighted Citation Impact
- 2.34
Funders
- Aarhus Universitet
- Innovationsfonden
- Carlsbergfondet
- Novo Nordisk
- Novo Nordisk Fonden