1. Differentiation of dopaminergic neural progenitor cells
- Thawing MD NPCs (midbrain dopaminergic neural progenitor cells)
- Prepare a BMM (basic matrix membrane)-coated plate and warm complete N2B27. Add 10 mL of warm DMEM/F12 to a 15 mL conical tube. Place a cryovial in a 37 °C heat block for 2 min.
- Transfer the cells from the cryovial to the tube containing DMEM/F12. Centrifuge at 300 x g for 5 min.
- Aspirate the supernatant, resuspend the cells in 2 mL of N2B27, and add the cell suspension to one well of the BMM-coated plate. Incubate the cells at 37 °C with 5% CO2.
2. Transduction of MD NPCs and the analysis of methylation changes
- Transduction of MD NPCs
- Transduce MD NPCs at 70% confluence with LV (lentiviral vector)-guide RNA/deactivated Cas9-DNMT3A (DNA methyltransferase enzyme 3A) vectors at MOI (multiplicity of infection) = 2. Replace the N2B27 medium 16h posttransduction.
- Add N2B27 with 5 µg/mL puromycin, 48 h after the transduction. Culture the cells for 3 weeks in N2B27 plus puromycin to obtain the stable MD NPC lines. Cells are ready for downstream applications (DNA, RNA, protein analyses, phenotypic characterization, freezing, and passaging).