The use of fetal astrocytes for gene delivery into brains with neurodegener
ative diseases has been suggested. Therefore, the effects of neurotransmitt
ers in the brain on such cells are of interest. The presence of D-1 (D-1A)
receptors and the effect of dopamine on a fetal human astrocyte cell line (
SVG cells) in vitro were examined. SVG cells expressed D-1 (D-1A), but not
D-5 (D-1B) receptors, as shown by RT-PCR. Exposure to dopamine, apomorphine
, and the specific D-1 agonist, SKF-38393, increased glial-derived neurotro
phic factor production of SVG cells, as well as intracellular free calcium.
Exposure to the specific D-1 antagonist, SCH 23390, blocked these effects.
Thus, if implanted into a brain region rich in dopamine, or if transfected
with the tyrosine hydroxylase gene, fetal astrocytes may serve as paracrin
e/autocrine cells capable of supplying critical growth factors to diseased
brain tissue. (C) 2001 Wiley-Liss, Inc.