, 2003). Cortices and hippocampi from E17.5 to E18.5 embryos were dissected in Hank’s balanced salt solution (HBSS) supplemented with HEPES (10 mM) and glucose (0.66 M; Sigma-Aldrich). Tissues were dissociated in papain (Worthington) supplemented with DNase I (100 mg/ml; Sigma-Aldrich) for 20 min at 37°C, Veliparib mw washed three times, and manually triturated in plating medium. Cells were then plated at 565 cells/mm2 on glass-bottom dishes coated with poly-D-lysine

(1 mg/ml; Sigma-Aldrich) and cultured in neurobasal medium supplemented with 2.5% fetal bovine serum (Gemini), B27 (1×), L-glutamine (2 mM), and penicillin (2.5 U/ml)-streptomycin (2.5 mg/ml) (Invitrogen). At 5 DIV, half of the medium was replaced with serum-free medium, and one-third of the medium was then changed every 5 days. At 7 DIV, 5-Fluoro-5′-deoxyuridine (Sigma-Aldrich) was added to the culture medium at a final concentration of 5 μM to limit glia proliferation. Cells were maintained at 37°C in 5% CO2 for 18–22 days. Neurons were transfected at 11 or 15 DIV by magnetofection using NeuroMag (OZ Bioscience), according to manufacturer’s instructions. Cotransfections were performed at a 1:1 ratio (w/w). Briefly, cDNA (2 μg final) was incubated with NeuroMag in neurobasal medium for 15 min at room temperature and then the mixture was applied dropwise on culture cells. Cultures were placed on a magnet for 20 min for transfection

(see Supplemental Information). Cell recordings were performed using a multiclamp 700B amplifier (Axon Instruments). Neurons were recorded in Protease Inhibitor Library supplier Parvulin a bath solution containing 140 mM NaCl, 5 mM KCl, 0.8 mM MgCl2, 10 mM HEPES, 2 mM CaCl2, and 10 mM glucose. The whole-cell internal solution contained 135 mM CsCl2, 10 mM HEPES, 1 mM EGTA, 4 mM Na-ATP, and 0.40 mM Na-GTP. Spontaneous mEPSCs were isolated by adding 0.2 mM picrotoxin and 0.1 mM tetrodotoxin in the recording bath solution and sampled in voltage-clamp configuration using pClamp 10 (Axon Instruments). Analyses were done offline using Clampfit 10 (Axon Instruments)

and Excel (Microsoft). For illustration purpose, traces were filtered at 200 Hz to remove noise. There were no differences in membrane capacitance (Cm) or input resting membrane resistance (Rm) among experimental groups: CONT (control, EGFP only), Cm = 71.12 ± 5.9 pF and Rm = 117.62 ± 7.2 MΩ (n = 16); CONT+Aβ42, Cm = 68.50 ± 4.4 pF and Rm = 105.28 ± 7.8 MΩ (n = 21); CAMKK2 KD, Cm = 67.66 ± 4.0 pF and Rm = 103.31 ± 8.2 MΩ (n = 18); and CAMKK2 KD+Aβ42, Cm = 83.95 ± 7.0 pF and Rm = 113.01 ± 8.0 MΩ (n = 16). In utero electroporation was performed as previously described by Yi et al. (2010) with slight modifications in order to target the embryonic hippocampus (see Supplemental Information). Images were acquired in 1,024 × 1,024 resolution with a Nikon Ti-E microscope equipped with the A1R laser-scanning confocal microscope using the Nikon software NIS-Elements (Nikon, Melville, NY, USA).