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Efficient transduction of neurons using Ross River glycoprotein-pseudotyped lentiviral vectors.

Author

Summary, in English

Lentiviral vectors are promising tools for CNS gene transfer since they efficiently transduce the cells of the nervous system in vivo. In this study, we have investigated the transduction efficiency of lentiviral vectors pseudotyped with Ross River virus glycoprotein (RRV-G) (RRV-G-pseudotyped lentiviral vectors (RRV-LV)). The RRV is an alphavirus with an extremely broad host range, including the cells of the central nervous system. Previous studies have shown that lentiviral vectors can be efficiently pseudotyped with this envelope protein and have demonstrated promising features of such vectors, including the possibility to establish stable producer cell lines. After injection of RRV-LV expressing green fluorescent protein into different structures in the rat brain we found efficient transduction of both neurons and glial cells. By using two cell-type-specific promoters, neuron-specific enolase and human glial fibrillary acidic protein, we demonstrated cell-specific transgene expression in the desired cell type. Ross River virus glycoprotein-pseudotyped lentiviral vectors also transduced human neural progenitor cells in vitro, showing that receptors for the RRV-G are present on human neural cells.

Publishing year

2006

Language

English

Pages

966-973

Publication/Series

Gene Therapy

Volume

13

Issue

12

Document type

Journal article

Publisher

Nature Publishing Group

Topic

  • Neurosciences

Keywords

  • green fluorescent protein
  • alphavirus
  • astrocyte
  • gene transfer

Status

Published

Research group

  • Neurobiology
  • CNS Gene Therapy

ISBN/ISSN/Other

  • ISSN: 0969-7128