Efficient transduction of neurons using Ross River glycoprotein-pseudotyped lentiviral vectors.
(2006) In Gene Therapy 13(12). p.966-973- Abstract
- 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... (More)
- 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. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/154854
- author
- Jakobsson, Johan LU ; Tolstrup Nielsen, Troels LU ; Staflin, Karin LU ; Georgievska, Biljana LU and Lundberg, Cecilia LU
- organization
- publishing date
- 2006
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- green fluorescent protein, alphavirus, astrocyte, gene transfer
- in
- Gene Therapy
- volume
- 13
- issue
- 12
- pages
- 966 - 973
- publisher
- Nature Publishing Group
- external identifiers
-
- pmid:16511527
- wos:000238041000004
- scopus:33744820829
- pmid:16511527
- ISSN
- 0969-7128
- DOI
- 10.1038/sj.gt.3302701
- language
- English
- LU publication?
- yes
- id
- cd164568-bebd-4f09-9556-3fb825f57e46 (old id 154854)
- alternative location
- http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=16511527&dopt=Abstract
- date added to LUP
- 2016-04-01 11:46:19
- date last changed
- 2022-01-26 18:02:14
@article{cd164568-bebd-4f09-9556-3fb825f57e46, abstract = {{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.}}, author = {{Jakobsson, Johan and Tolstrup Nielsen, Troels and Staflin, Karin and Georgievska, Biljana and Lundberg, Cecilia}}, issn = {{0969-7128}}, keywords = {{green fluorescent protein; alphavirus; astrocyte; gene transfer}}, language = {{eng}}, number = {{12}}, pages = {{966--973}}, publisher = {{Nature Publishing Group}}, series = {{Gene Therapy}}, title = {{Efficient transduction of neurons using Ross River glycoprotein-pseudotyped lentiviral vectors.}}, url = {{http://dx.doi.org/10.1038/sj.gt.3302701}}, doi = {{10.1038/sj.gt.3302701}}, volume = {{13}}, year = {{2006}}, }