Adeno-associated virus vector-mediated bcl-2 gene transfer info post-ischemic gerbil brain in vivo: prospects for gene therapy of ischemia-induced neuronal death

被引:72
作者
Shimazaki, K
Urabe, M
Monahan, J
Ozawa, K
Kawai, N
机构
[1] Jichi Med Sch, Dept Physiol, Minami Kawachi, Tochigi 3290498, Japan
[2] Jichi Med Sch, Ctr Mol Med, Div Genet Therapeut, Minami Kawachi, Tochigi 3290498, Japan
[3] Jichi Med Sch, Dept Hematol, Minami Kawachi, Tochigi 3290498, Japan
[4] Avigen Inc, Alameda, CA USA
关键词
adeno-associated virus vector; bcl-2; hippocampus; ischemia; delayed neuronal death;
D O I
10.1038/sj.gt.3301211
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The proto-oncogene bcl-2 is known as an anti-apoptotic gene that confers the ability to block neuronal cell death after transient ischemia. In order to examine whether the bcl-2 gene can be used for protection of ischemic brain injury, we generated adeno-associated virus (AAV) vectors capable of expressing human bcl-2. Replication-defective AAV Vectors were found effectively to transfer and express bcl-2 gene in the gerbil hippocampal neurons. Transduction with AAV bcl-2 5 days before forebrain ischemia prevented the DNA fragmentation in the CA1 neurons that is commonly associated with ischemia-induced cell death. Furthermore, the application of AAV bcl-2 as late as Ih following an ischemic insult also prevented DNA fragmentation in CA1 neurons. These results suggest that the bcl-2 protein has neuroprotective functions that inhibit ischemic cell death and demonstrate the potential of AAV bcl-2 for use in post-ischemic gene therapy in the brain.
引用
收藏
页码:1244 / 1249
页数:6
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