M. Meyer et al., Improved survival of embryonic porcine dopaminergic neurons in coculture with a conditionally immortalized GDNF-producing hippocampal cell line, EXP NEUROL, 164(1), 2000, pp. 82-93
Transplantation of embryonic nigral tissue is used as an experimental thera
py for patients with Parkinson's disease but is hampered by a limited survi
val rate of dopaminergic neurons. Glial cell line-derived neurotrophic fact
or (GDNF) is a potent survival factor for nigrostriatal dopaminergic neuron
s, and the present in vitro study aimed at improving the survival of dopami
nergic neurons in porcine mesencephalic brain slice cultures by adding tran
sfected, immortalized, temperature-sensitive GDNF-releasing HiB5 cells (HiB
5-GDNF). Embryonic (E27/28) porcine ventral mesencephalic brain slices were
placed on membrane inserts in six-well plates with serum-containing medium
, and HiB5-GDNF, nontransfected HiB5 cells (HiB5-control), or green fluores
cent protein-producing HiB5 cells (HiB5-GFP) were seeded onto each tissue s
lice. The concentration of GDNF in the coculture medium was 0.49 +/- 0.13 n
g/ml at day 9 and 0.22 +/- 0.05 ng/ml at day 19 (mean +/- SEM) as measured
by GDNF ELISA, The decrease in release of GDNF over time was paralleled by
a gradual reduction in the number of HiB5-GFP cells expressing the reporter
gene (EGFP). At day 12, HPLC analysis revealed that medium from HiB5-GDNF
cocultures contained 2.0 times more dopamine than medium from HiB5-control
cocultures. At day 21 there was 1.6 times more dopamine. Similar results we
re obtained for the dopamine metabolite 3,4-dihydroxyphenylacetic acid. At
day 21, cell counts showed that HiB5-GDNF cocultures contained 1.5 times mo
re tyrosine hydroxylase immunoreactive neurons than HiB5-control cocultures
, which must be compared with a 1.8 fold increase after chronic treatment w
ith rhGDNF (10 ng/ml). In conclusion, the better survival of HiB5-GDNF cocu
ltures is promising for the generation of effective cell lines for local de
livery of neurotrophic factors to intracerebral nigral grafts. (C) 2000 Aca
demic Press.