Influence of time in culture and BDNF pretreatment on survival and function of grafted embryonic rat ventral mesencephalon in the 6-OHDA rat model ofParkinson's disease
Gu. Hoglinger et al., Influence of time in culture and BDNF pretreatment on survival and function of grafted embryonic rat ventral mesencephalon in the 6-OHDA rat model ofParkinson's disease, EXP NEUROL, 167(1), 2001, pp. 148-157
Embryonic midbrain can be maintained as free-floating roller tube cultures
prior to grafting in experimental Parkinson's disease. We examined the infl
uence of pregrafting culture time and pretreatment with brain-derived neuro
trophic factor on graft survival and function. Cultures were prepared from
solid pieces of embryonic (E14) rat ventral mesencephalon and maintained 4,
8, or 12 days in vitro with or without brain-derived neurotrophic factor (
100 ng/ml) and grafted into the striatum of 6-hydroxydopamine-lesioned rats
. Graft survival and function were evaluated by amphetamine-induced rotatio
n behavior, number of tyrosine hydroxylase-immunoreactive neurons, striatal
reinnervation, and graft volume. Rats receiving untreated tissue cultured
for 4 or 8 days displayed no differences in graft quality, while grafts fro
m 12-day-old cultures contained significantly fewer (P < 0.05) tyrosine hyd
roxylase-immunoreactive neurons (340 +/- 97, 267 +/- 92, and 62 +/- 19) and
displayed a lower survival rate (9.6 +/- 2.7, 7.9 +/- 2.7, and 2.6 +/- 0.8
% for 4, 8, and 12 days in vitro, respectively). Only rats grafted with 4-
and 8-day-old cultures recovered significantly (P < 0.05) from lesion-induc
ed rotations (69.4 +/- 18.6, 70.3 +/- 13.9, and 23.2 +/- 12.1% for 4, 8, an
d 12 days in vitro, respectively). Striatal reinnervation decreased with in
creasing culture time (P < 0.05). Pretreatment of the cultures with brain-d
erived neurotrophic factor affected only graft-induced fiber reinnervation,
which was reduced even after short culture times. We therefore suggest tha
t a storage period of 8 days is well suited to maintain embryonic rat ventr
al mesencephalon with the free-floating roller tube culture technique prior
to transplantation. BDNF pretreatment as a new strategy to improve graft s
urvival and function, however, was not effective. (C) 2001 Academic Press.