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. 2010 Sep 20;285(48):37293–37301. doi: 10.1074/jbc.M110.157081

FIGURE 1.

FIGURE 1.

Neural stem cells prepared in the form of neurospheres. a, neurospheres were prepared from the striata of mouse embryos (embryonic day 14.5) and cultured in Neurobasal-A medium supplemented with B27, basic FGF and EGF. b, cells forming neurospheres were stained with Rat 401 anti-nestin antibody or AK97 anti-SSEA-1 antibody. Most neurosphere-forming cells were positive for nestin (neural stem cell marker protein; green) and SSEA-1 (neural stem cell marker carbohydrate; green). coIgG and coIgM indicate subclass control IgG and control IgM (BD Biosciences), respectively. c, cells forming neurospheres were cultured in undifferentiation condition (undiffer) or differentiation condition (differ; 0 ng/ml basic FGF and EGF and 1% fetal bovine serum for 5 days) and then stained with antibodies to nestin, β-III tubulin, glial fibrillary acidic protein (GFAP), and galactocerebroside (GalC). β-III Tubulin+ neurons (green), GFAP+ astrocytes (green), and GalC+ oligodendrocytes (green) are found in the cells cultured in differentiation condition. Nuclei were stained with Hoechst 33258 (blue). Scale bars, 100 μm in a; 50 μm in b and c.