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3 protocols using l glutamine substitute glutamax

1

Neuronal Culture and Transduction Protocol

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Pregnant rats (E17) of the Sprague-Dawley strain were purchased from Charles River. Embryos were surgically removed from the mothers and cortices dissected in Hanks Balanced salt solution (Gibco). The meninges were removed and cells dissociated using a papain dissociation system (Worthington) before being resuspended in Neurobasal medium A supplemented with antibiotic-antimycotic solution (Gibco), L-glutamine substitute (GlutaMAX™; Gibco) and factor B27 (Gibco). Cells were plated on poly-D-lysine coated glass coverslips at a density of 5 × 105 cells/well and incubated at 37 °C in 5% CO2 with half media changes every 3 days. Cells were transduced with AAV-A53T, AAV-Empty and AAV-UbG76V-GFP 2 days post-isolation at a multiplicity of infection (MOI) of 3000. Media containing AAV vectors were removed after 72 h and cells were fixed with 4% PFA for immunofluorescence staining at 8 days post-isolation.
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Rat Cortical Neuron Culture and Transduction

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Pregnant rats (E17) of the Sprague-Dawley strain were purchased from Envigo. Embryos were surgically removed from the mothers and cortices dissected in Hanks Balanced salt solution (Gibco). The meninges were removed, and cells were dissociated using a papain dissociation system (Worthington) before being resuspended in Neurobasal medium A supplemented with antibiotic-antimycotic solution (Gibco), L-glutamine substitute (GlutaMAX™; Gibco) and factor B27 (Gibco). Cells were plated on poly-D-lysine coated glass coverslips at a density of 5 × 105 cells/well, or on poly-D-lysine coated six-well cell culture plates at a density of 2 × 106 cells/well, and incubated at 37 °C in 5% CO2 with half media changes every 3 days. Cells were transduced with A53T a-syn or EV AAVs at 2 days post-isolation at a MOI of 3000. After 3 days, media containing AAV vectors were removed. Cells were transduced with Scramble1.3 or PDpep1.3 AAVs at 2- or 5-days post-isolation at a MOI of 3000. Cells were fixed with 4% paraformaldehyde (PFA) for immunofluorescence staining or lysed for immunoblotting at 8 days post-isolation.
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3

Primary Neuronal Culture from Rat Embryos

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Pregnant Sprague-Dawley rats (E17) were purchased from Envigo. Embryos were surgically removed and cortices dissected in Hanks Balanced salt solution (Gibco). The meninges were removed, and cells were dissociated using a papain dissociation system (Worthington) before being resuspended in Neurobasal medium A supplemented with antibiotic-antimycotic solution (Gibco), L-glutamine substitute (Gluta-MAX™; Gibco) and factor B27 (Gibco). Neurons were plated on poly-Dlysine coated glass coverslips at a density of 5 × 10 5 cells/well, or on poly-D-lysine coated 6-well cell culture plates at a density of 2 × 10 6 cells/well and incubated at 37 • C in 5% CO 2 with half media changes every 3 days. Cells were transduced with AAVs 2 days post-isolation at a multiplicity of infection of 3000. Media containing AAV vectors was removed after 72 h and replaced with fresh media 5 days post-isolation. Following stimulation protocol (see below), neurons were immediately fixed with 4% paraformaldehyde (PFA) for immunofluorescence staining or lysed for immunoblotting.
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