Abstract
Serum-free culture conditions for retinoic acid-induced neural differentiation of mouse P19 embryonal carcinoma cells were determined for future ex vivo retroviral gene transfer and brain transplantation studies. Neural differentiation of P19 cells was dependent on the seeding densities, and both neurons and astroglia differentiated efficiently at high seeding densities (2 × 104 and 5 × 104 cells/cm2) but not at low seeding density (1 × 104 cells/cm2). In addition, P19 cells cultured at 5 × 104 cells/cm2 showed neural differentiation whether or not they were infected with Friend leukemia virus FrC6-V, which inhibited neural differentiation at 2 × 104 cells/cm2. These results indicate that FrC6-V-infected P19 embryonal carcinoma cells should be seeded at high density to achieve efficient neural differentiation in vitro for ex vivo gene transfer with a FrC6-V–derived retroviral vector system.
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