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To develop lentiviral vectors for transducing neural stem cells (NSCs) in vivo, we produced a replication-incompetent recombinant lentiviral vector for pseudotyping with the vesicular stomatitis virus glycoprotein (VSV-G). Lentiviral vectors encoding green fluorescent protein (GFP) were pseudotyped with the vesicular stomatitis virus glycoprotein (VSV-G). We then transduced neural stem/progenitor cells, including neuronal stem cells and progenitor cells isolated from rat hippocampus, using these lentiviral vectors and analyzed transgene expression by immunohistochemical analyses. We observed GFP-expressing cells in the dentate gyrus and subventricular zone at 1 week after lentiviral vector administration. Cells expressing green fluorescent protein were restricted to the subventricular zone, which included neural stem cells, at 4 weeks. Immunohistochemical analyses of the cells expressing GFP indicated that these cells were positive for markers of neural stem/progenitor cells, including nestin, O4 and Ki67. The expression of GFP was observed mainly in the neural stem/progenitor cells but not in astrocytes. Our be359ba680
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