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

Citation
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
Citations number
52
Categorie Soggetti
Neurosciences & Behavoir
Journal title
EXPERIMENTAL NEUROLOGY
ISSN journal
00144886 → ACNP
Volume
167
Issue
1
Year of publication
2001
Pages
148 - 157
Database
ISI
SICI code
0014-4886(200101)167:1<148:IOTICA>2.0.ZU;2-V
Abstract
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.