Masamizu Yoshito, Okada Takashi, Ishibashi Hidetoshi, Takeda Shin'ichi, Yuasa Shigeki, Nakahara Kiyoshi
Department of Animal Models for Human Disease, National Institute of Neuroscience, NCNP, Tokyo, Japan.
Neuroreport. 2010 Apr 21;21(6):447-51. doi: 10.1097/WNR.0b013e328338ba00.
Although the adeno-associated virus (AAV) vector is a promising tool for gene transfer into neurons, especially for therapeutic purposes, neurotropism in primate brains is not fully elucidated for specific AAV serotypes. Here, we injected AAV serotype 8 (AAV8) vector carrying the enhanced green fluorescent protein (EGFP) gene under a ubiquitous promoter into the cerebral cortex, striatum and substantia nigra of common marmosets. Robust neuronal EGFP expression was observed at all injected sites. Cell typing with immunohistochemistry confirmed efficient AAV8-mediated gene transfer into the pyramidal neurons in the cortex, calbindin-positive medium spiny neurons in the striatum and dopaminergic neurons in the substantia nigra. The results indicate a preferential tropism of AAV8 for subsets of neurons, but not for glia, in monkey brains.
尽管腺相关病毒(AAV)载体是一种将基因导入神经元的有前景的工具,特别是用于治疗目的,但特定AAV血清型在灵长类动物大脑中的嗜神经特性尚未完全阐明。在这里,我们将携带增强型绿色荧光蛋白(EGFP)基因的AAV血清型8(AAV8)载体在遍在启动子的调控下注射到普通狨猴的大脑皮层、纹状体和黑质中。在所有注射部位均观察到强烈的神经元EGFP表达。免疫组织化学细胞分型证实AAV8介导的基因有效导入到皮层中的锥体神经元、纹状体中钙结合蛋白阳性的中等棘状神经元以及黑质中的多巴胺能神经元。结果表明,在猴脑中,AAV8对神经元亚群具有优先嗜性,而对神经胶质细胞没有优先嗜性。