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Adenovirus-mediated transduction with hGDNF prevents
MPTP-induced dopamine depletion in striatum of mouse brain.
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As a novel trial of neuroprotective therapy of neurodegenerative diseases,
we have constructed a recombinant adenovirus vector (rAdv) bearing a
neurotrophic factor gene to deliver the factor to rescue neurons in vivo.

In the present study, human glial cell line-derived neurotrophic factor
(hGDNF) was chosen to examine the applicability of our strategy to a mouse
model of Parkinson's disease.

During the construction of the rAdv, we found that the strong constitutive
hGDNF expression unit somehow inhibited the appearance of the rAdv.

Therefore we adopted a self-contained tetracycline-regulated expression
system to acquire an rAdv expressing hGDNF.

By analyzing the condition medium of SH-SY5Y cells infected with our
constructed virus vector, we confirmed that biologically active GDNF was
successfully expressed in vitro.

For an animal study, we delivered this virus vector directly to the C57
black mouse brain and then exposed the animal to
1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) to injure the
nigrostriatal dopaminergic neurons.

One week after the MPTP exposure, the neuroprotective effect of the virus
vector was estimated by measurement of the dopamine content in the striatum
of the mouse brain.

The mice that had received our constructed virus had significantly higher
dopamine levels in their striatum, demonstrating that our rAdv expressing
hGDNF has therapeutic potential to protect the nigrostriatal dopaminergic
neurons in vivo.


Copyright 1997 Academic Press
Biochem Biophys Res Commun 1997 Sep 18;238(2):569-573
Kojima H, Abiru Y, Sakajiri K, Watabe K, Ohishi N,
Takamori M, Hatanaka H, Yagi K
Gifu International Institute of Biotechnology, Gifu, Japan
PMID: 9299553, MUID: 97446026
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