The aggregated culture contains multiple layers of cells, making it difficult for the testing reagents and antibodies to access the cultured cells for later quantification. Recently, a dissociated neuron-OL co-culture model from mouse embroynic spinal cord

has been described (Thomson et al. 2008). Interestingly, the authors noted also that such culture derived from embryonic rat spinal cord tissue failed to myelinate. Here, we described a novel modified Inhibitors,research,lifescience,medical neuron-OL co-culture rat model that can be utilized to investigate the mechanisms of CNS-related myelin deficits. Material and Methods Chemicals Dulbecco’s modified Eagle Medium (DMEM)/Ham’s F12, neural basal medium (NBM), B27 supplement, 7.5% bovine serum albumin (BSA), Hank’s Balanced Inhibitors,research,lifescience,medical Salt Solution (HBSS), and penicillin/streptomycin were purchased from Invitrogen (Carlsbad, CA, USA). Recombinant rat nerve growth factor (NGF), neurotrophin-3 (NT-3), tumor necrosis factor-α (TNFα), and interleukin-1β (IL-1β), were obtained from R&D system (Minneapolis, MN, USA). Normal horse and fetal bovine serum, insulin, transferrin, sodium selenium, progesterone, putrescine, GDC-0973 ic50 hydrocortisone, Inhibitors,research,lifescience,medical biotin, N-acetyl-L-cysteine, triiodothyronine (T3), L-α-Lysophosphatidylcholine (LPC) were

obtained from Sigma-Aldrich (St. Louis, MO, USA). Normal guinea pig serum was from EMD Chemicals (Philadelphia, PA, USA). The sources and specificity of primary antibodies are listed in Table 1. Second antibodies (biotin or fluorescein labeled) were obtained from Jackson ImmunoResearch Inhibitors,research,lifescience,medical Lab (West Grove, PA, USA). Table 1 Antibodies used in immunocytochemistry in this study Myelination co-culture The dissection of rat E16 spinal cord is similar to that described previously in mice (Thomson et al. 2008). Briefly, spinal cords from six embryos Inhibitors,research,lifescience,medical were collected in a petri dish containing

1 mL of 1× HBSS (without Ca2+ and Mg2+). After carefully removing the meninges, the spinal cord tissue was cut into small pieces using a surgical blade. The minced tissue were then transferred into a 15-mL centrifuge tube with 1 mL Trypsin-EDTA (Sigma #T4299) and incubated for 15 min at 37°C. The enzymatic reaction was stopped by mixing the tissue with 1.5-mL trypsin through inhibitor-DNase I solution (0.05% soybean trypsin inhibitor, 0.02% DNase-I, and 0.3% BSA in DMEM), and tissue suspension was centrifuged at 800 g for 5 min. The supernatant was replaced with 5-mL plating medium (50% normal horse serum and 20% 1× HBSS with Ca2+/Mg2+ in DMEM). Tissue was titrated with a 1-mL pipette tip for 10 times. The dissociated cell suspension was then passed through a 40-μm cell strainer. Total number of cells was counted by mixing one part of cell suspension with one part of trypan blue solution. The viable cells typically exceeded 80%. Cells were then seeded on poly-L-lysine-coated cover slips at a density of 0.4 × 105/cm2.