Glial cell line-derived neurotrophic factor-supplemented hibernation of fetal ventral mesencephalic neurons for transplantation in Parkinson disease: long-term storage

被引:21
作者
Hebb, AO
Hebb, K
Ramachandran, AC
Mendez, I
机构
[1] Dalhousie Univ, Dept Anat, Fac Med, Halifax, NS B3H 4H7, Canada
[2] Dalhousie Univ, Dept Neurobiol, Fac Med, Halifax, NS B3H 4H7, Canada
[3] Dalhousie Univ, Dept Surg, Fac Med, Div Neurosurg, Halifax, NS B3H 4H7, Canada
关键词
glial cell line-derived neurotrophic factor; neural transplantation; hibernation; Parkinson disease; rat;
D O I
10.3171/jns.2003.98.5.1078
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Object. Transplantation of fetal dopaminergic tissue is being investigated in animal models and clinical trials for its potential as a treatment for advanced Parkinson disease. At the same time, the availability of fetal tissue is limited, making its storage time prior to transplantation a key practical issue. Although it results in a smaller percentage of surviving cells, a longer storage time enables fetal tissue obtained over several days to be pooled for transplantation in a recipient. Glial cell line-derived neurotrophic factor (GDNF) has been shown to improve survival of human dopaminergic tissue that has been stored prior to transplantation. The objective of this study was to evaluate the effects on fetal dopaminergic tissue of GDNF-supplemented hibernation for extended periods of 6 to 15 days. Methods. The ventral mesencephalon (VM) was harvested in a total of 27 14-day-old rat fetuses, and three VMs were cultured immediately (fresh control group). The remaining 24 VMs were divided sagittally along the midline to yield 48 equal pieces of hemimesencephalon. Twenty-four pieces were stored with GDNF-supplemented hibernation medium for 6, 9, 12, or 15 days, and the 24 "partner" hemimesencephalon pieces were stored in control hibernation medium for the same periods of time. Tissue was cultured for 48 hours and processed for tyrosine hydroxylase (TH) immunoreactivity and double-stained with cresyl violet. Cell counts for all cultures and the percentage of TH-immunoreactive cells were obtained. The percentage of TH-immunoreactive cells for the fresh control group was 6.3 +/- 0.5%. The percentage of TH-immunoreactive cells in cultures derived from tissue stored in GDNF-supplemented medium was significantly increased at 6 and 9 days posthibernation compared with the fresh control group and the "partner" groups stored in hibernation medium only. No significant increase in the percentage of TH-immunoreactive cells was observed in the 12- and 15-day groups. Conclusions. In this study the authors have demonstrated that fetal dopaminergic tissue can be safely stored for up to 9 days in GDNF-supplemented hibernation medium. Furthermore, the percentage of TH-immunoreactive cells is significantly increased after 6 and 9 days of storage in this medium, improving the yield of TH-immunoreactive cells prior to transplantation. These observations have practical clinical implications for collecting fetal dopaminergic cells and improving their survival after transplantation.
引用
收藏
页码:1078 / 1083
页数:6
相关论文
共 61 条
[1]   Glial cell line-derived neurotrophic factor improves intrastriatal graft survival of stored dopaminergic cells [J].
Apostolides, C ;
Sanford, E ;
Hong, M ;
Mendez, I .
NEUROSCIENCE, 1998, 83 (02) :363-372
[2]   RECONSTRUCTION OF THE NIGROSTRIATAL DOPAMINE PATHWAY BY INTRA-CEREBRAL NIGRAL TRANSPLANTS [J].
BJORKLUND, A ;
STENEVI, U .
BRAIN RESEARCH, 1979, 177 (03) :555-560
[3]  
BRUNDIN P, 1988, EXP BRAIN RES, V70, P192
[4]   CRYOPRESERVATION AND STORAGE OF EMBRYONIC RAT MESENCEPHALIC DOPAMINE NEURONS FOR ONE-YEAR - COMPARISON TO FRESH TISSUE IN CULTURE AND NEURAL GRAFTS [J].
COLLIER, TJ ;
GALLAGHER, MJ ;
SLADEK, CD .
BRAIN RESEARCH, 1993, 623 (02) :249-256
[5]   SUSCEPTIBILITY OF HUMAN FETAL BRAIN-TISSUE TO COOL-STORAGE AND FREEZE-STORAGE [J].
DONG, JF ;
DETTA, A ;
HITCHCOCK, ER .
BRAIN RESEARCH, 1993, 621 (02) :242-248
[6]   GDNF signalling through the Ret receptor tyrosine kinase [J].
Durbec, P ;
MarcosGutierrez, CV ;
Kilkenny, C ;
Grigoriou, M ;
Wartiovaara, K ;
Suvanto, P ;
Smith, D ;
Ponder, B ;
Costantini, F ;
Saarma, M ;
Sariola, H ;
Pachnis, V .
NATURE, 1996, 381 (6585) :789-793
[7]   Glial cell line-derived neurotrophic factor protects dopaminergic neurons from 6-hydroxydopamine toxicity in vitro [J].
Eggert, K ;
Schlegel, J ;
Oertel, W ;
Würz, C ;
Krieg, JC ;
Vedder, H .
NEUROSCIENCE LETTERS, 1999, 269 (03) :178-182
[8]  
Freed C. R., 1996, Society for Neuroscience Abstracts, V22, P1210
[9]   Transplantation of embryonic dopamine neurons for severe Parkinson's disease. [J].
Freed, CR ;
Greene, PE ;
Breeze, RE ;
Tsai, WY ;
DuMouchel, W ;
Kao, R ;
Dillon, S ;
Winfield, H ;
Culver, S ;
Trojanowski, JQ ;
Eidelberg, D ;
Fahn, S .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (10) :710-719
[10]   BILATERAL FETAL NIGRAL TRANSPLANTATION INTO THE POSTCOMMISSURAL PUTAMEN IN PARKINSONS-DISEASE [J].
FREEMAN, TB ;
OLANOW, CW ;
HAUSER, RA ;
NAUERT, GM ;
SMITH, DA ;
BORLONGAN, CV ;
SANBERG, PR ;
HOLT, DA ;
KORDOWER, JH ;
VINGERHOETS, JG ;
SNOW, BJ ;
CALNE, D ;
GAUGER, LI .
ANNALS OF NEUROLOGY, 1995, 38 (03) :379-388