Cerebellar granule cells offer a useful model system to study the effe
cts of neurotrophins during development. We have used a defective herp
es simplex virus type 1 (HSV-1) vector containing brain-derived neurot
rophic factor (BDNF) to ex-press this neurotrophin in aggregate cultur
es of granule cells. Viral infection led to easily detectable BDNF exp
ression and neurite outgrowth of granule cells, expressing the high af
finity receptor TrkB. Neurite elongation mediated by the HSV-1 vector
producing BDNF was similar to that found after exposure to purified BD
NF. This study demonstrates the efficacy of HSV-1 vectors for delivery
and expression of neurotrophins in cerebellar granule cells. The biol
ogical responses measured indicate the effectiveness of HSV-1 vectors
as potential therapeutic tools.