Comparative study of GDNF delivery systems for the CNS:: polymer rods, encapsulated cells, and lentiviral vectors

被引:35
作者
Bensadoun, JC
de Almeida, LP
Fine, EG
Tseng, JL
Déglon, N
Aebischer, P [1 ]
机构
[1] Swiss Fed Inst Technol, Inst Neurosci, EPFL, CH-1015 Lausanne, Switzerland
[2] Univ Lausanne, Sch Med, Div Surg Res, Lausanne, Switzerland
[3] Univ Lausanne, Sch Med, Gene Therapy Ctr, Lausanne, Switzerland
[4] Univ Coimbra, Pharmaceut Technol Lab, Fac Pharm, Coimbra, Portugal
[5] Univ Coimbra, Ctr Neurosci, Coimbra, Portugal
关键词
CNS delivery; neurotrophic factors; polymer rods; cell encapsulation; lentiviral vectors;
D O I
10.1016/S0168-3659(02)00353-X
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Glial cell line-derived neurotrophic factor (GDNF) holds great promise for the treatment of Parkinson's disease. In humans, its intracerebroventricular administration leads to limiting side effects. Direct parenchymal delivery using mechanical means, or cell and gene therapy represent potential alternatives. In the present study, a representative of each of these three approaches, i.e. polymer rods, genetically modified encapsulated cells and lentiviral vectors was analyzed for its ability to release GDNF in the striatum of rats. One week post-surgery, GDNF was detected over a distance of 4 mm with all three methods. At 4 weeks GDNF staining diminished with rods and to a lesser extent with encapsulated cells, whereas it increased with lentiviral vectors. Nanogram range of GDNF was measured with all methods at I week. At 4 weeks, GDNF levels decreased significantly with rods, whereas they remained stable with encapsulated cells and lentiviral vectors. We conclude that all three methods investigated allow striatal delivery of GDNF, but the time during which it needs to be released will determine the approach chosen for clinical application. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:107 / 115
页数:9
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