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Here, we treated hDAT cells with AA along with an oxidizing solution containing Fe +3 (197 m) plus ascorbate (19.7 mm, Fe +3 /Asc

H 2 O 2 treatment upregulated the expression of APP gene both in D-iNs and E-iNs, but the effect was more prominent in D-iNs (Fig

When the cell confluence reached 80%, the cells were subcultured onto either a Transwell plate (Corning Inc.) for the permeability assay or a six-well plate (Corning Inc.) for the western blot