Direct in vivo gene transfer to ependymal cells in the central nervous system using recombinant adenovirus vectors
- PMID: 8485578
- DOI: 10.1038/ng0393-229
Direct in vivo gene transfer to ependymal cells in the central nervous system using recombinant adenovirus vectors
Abstract
To evaluate the potential for adenovirus-mediated central nervous system (CNS) gene transfer, the replication deficient recombinant adenovirus vectors Ad.RSV beta gal (coding for beta-galactosidase) and Ad-alpha 1AT (coding for human alpha 1-antitrypsin) were administered to the lateral ventricle of rats. Ad.RSV beta gal transferred beta-galactosidase to ependymal cells lining the ventricles whereas Ad-alpha 1AT mediated alpha 1-antitrypsin secretion into the cerebral spinal fluid for 1 week. These observations, together with beta-galactosidase activity in the globus pallidus and substantia nigra following stereotactic administration of Ad.RSV beta gal to the globus pallidus, suggest that adenovirus vectors will be useful for CNS gene therapy.
Comment in
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Gene delivery into the brain using virus vectors.Nat Genet. 1993 Mar;3(3):187-9. doi: 10.1038/ng0393-187. Nat Genet. 1993. PMID: 8485570 No abstract available.
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