Efficient transduction of neural cells in vitro and in vivo by a baculovirus-derived vector.

Abstract:

:Gene delivery to the central nervous system is central to the development of gene therapy for neurological diseases. We developed a baculovirus-derived vector, the Bac-CMV-GFP vector, containing a reporter gene encoding for the green fluorescent protein (GFP) under the control of the cytomegalovirus (CMV) promoter. Two neuroblastomal cell lines and three human primary neural cultures could be efficiently transduced. In all cases, addition of butyrate, an inhibitor of histone deacetylase, increased the level of expression in terms of the number of GFP-expressing cells and the intensity of fluorescence. The level of expression in a human telencephalic culture was over 50% of transduced cells with a multiplicity of infection of 25. GFP expression was demonstrated to be genuine expression and not pseudotransduction of the reporter protein. Most interestingly, Bac-CMV-GFP could transduce neural cells in vivo when directly injected into the brain of rodents and was not inactivated by the complement system. Thus, baculovirus is a promising tool for gene transfer into the central nervous system both for studies of the function of foreign genes and the development of gene therapy strategies.

authors

Sarkis C,Serguera C,Petres S,Buchet D,Ridet JL,Edelman L,Mallet J

doi

10.1073/pnas.260472897

keywords:

subject

Has Abstract

pub_date

2000-12-19 00:00:00

pages

14638-43

issue

26

eissn

0027-8424

issn

1091-6490

pii

260472897

journal_volume

97

pub_type

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